Medical Billing Code Search
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9172 results found
| G8752 | Sys bp less 140 | Description: Most recent systolic blood pressure < 140 mmhg |
| G8753 | Sys bp > or = 140 | Description: Most recent systolic blood pressure >= 140 mmhg |
| G8754 | Dias bp less 90 | Description: Most recent diastolic blood pressure < 90 mmhg |
| G8755 | Dias bp > or = 90 | Description: Most recent diastolic blood pressure >= 90 mmhg |
| G8756 | No bp measure doc | Description: No documentation of blood pressure measurement, reason not given |
| G8757 | Copd mg qual act perform | Description: All quality actions for the applicable measures in the chronic obstructive pulmonary disease (copd) measures group have been performed for this patient |
| G8758 | Ibd mg qual act perform | Description: All quality actions for the applicable measures in the inflammatory bowel disease (ibd) measures group have been performed for this patient |
| G8759 | Osa mg qual act perform | Description: All quality actions for the applicable measures in the sleep apnea measures group have been performed for this patient |
| G8761 | Dementia mg qual act perform | Description: All quality actions for the applicable measures in the dementia measures group have been performed for this patient |
| G8762 | Pd mg qual act perform | Description: All quality actions for the applicable measures in the parkinson's disease measures group have been performed for this patient |
| G8763 | Hyperten mg qual act perform | Description: All quality actions for the applicable measures in the hypertension (htn) measures group have been performed for this patient |
| G8764 | Car prev mg qual act perform | Description: All quality actions for the applicable measures in the cardiovascular prevention measures group have bee performed for this patient |
| G8765 | Cataract mg qual act perform | Description: All quality actions for the applicable measures in the cataract measures group have been performed for this patient |
| G8767 | Lipid panel res doc rev | Description: Lipid panel results documented and reviewed (must include total cholesterol, hdl-c, triglycerides and calculated ldl-c) |
| G8768 | Doc med reas no lipid profle | Description: Documentation of medical reason(s) for not performing lipid profile (e.g., patients with palliative goals or for whom treatment of hypertension with standard treatment goals is not clinically appropriate) |
| G8769 | Lipid profile not perform | Description: Lipid profile not performed, reason not given |
| G8770 | Urine protein test doc rev | Description: Urine protein test result documented and reviewed |
| G8771 | Doc dx ckd | Description: Documentation of diagnosis of chronic kidney disease |
| G8772 | Doc med reas no urine protn | Description: Documentation of medical reason(s) for not performing urine protein test (e.g., patients with palliative goals or for whom treatment of hypertension with standard treatment goals is not cllinically appropriate) |
| G8773 | No urine protein test | Description: Urine protein test was not performed, reason not given |
| G8774 | Serum creatinine doc rev | Description: Serum creatinine test result documented and reviewed |
| G8775 | Doc med reas no serum crtn | Description: Documentation of medical reason(s) for not performing serum creatinine test (e.g., patients with palliative goals or for whom treatment of hypertension with standard treatment goals is not clinically appropriate) |
| G8776 | No serum creatinine test | Description: Serum creatinine test not performed, reason not given |
| G8777 | Diabetes screen | Description: Diabetes screening test performed |
| G8778 | Doc med reas no diabete scrn | Description: Documentation of medical reason(s) for not performing diabetes screening test (e.g., patients with a diagnosis of diabetes, or with palliative goals or for whom treatment of hypertension with standard treatment goals is not clinically appropriate) |
| G8779 | No diabetes screen | Description: Diabetes screening test not performed, reason not given |
| G8780 | Counsel diet phys activity | Description: Counseling for diet and physical activity performed |
| G8781 | Doc med reas no counsel diet | Description: Documentation of medical reason(s) for patient not receiving counseling for diet and physical activity (e.g., patients with palliative goals or for whom treatment of hypertension with standard treatment goals is not clinically appropriate) |
| G8782 | No counsel diet phys act | Description: Counseling for diet and physical activity not performed, reason not given |
| G8783 | Bp scrn perf rec interval | Description: Normal blood pressure reading documented, follow-up not required |
| G8784 | Pt no elig for bp assess | Description: Patient not eligible (e.g., documentation the patient is not eligible due to active diagnosis of hypertension, patient refuses, urgent or emergent situation) |
| G8785 | Bp scrn no perf at interval | Description: Blood pressure reading not documented, reason not given |
| G8797 | Specimen site not esophagus | Description: Specimen site other than anatomic location of esophagus |
| G8798 | Specimen site not prostate | Description: Specimen site other than anatomic location of prostate |
| G8806 | Perf ultrsnd to lct preg doc | Description: Performance of trans-abdominal or trans-vaginal ultrasound and pregnancy location documented |
| G8807 | No ta tv ultrasnd | Description: Trans-abdominal or trans-vaginal ultrasound not performed for reasons documented by clinician (e.g., patient has a documented intrauterine pregnancy [iup]) |
| G8808 | Ultrasound not perf, rng | Description: Trans-abdominal or trans-vaginal ultrasound not performed, reason not given |
| G8809 | Rh-immunoglobulin order | Description: Rh-immunoglobulin (rhogam) ordered |
| G8810 | Doc reas no rh-immuno | Description: Rh-immunoglobulin (rhogam) not ordered for reasons documented by clinician (e.g., patient had prior documented receipt of rhogam within 12 weeks, patient refusal) |
| G8811 | No rh-immunoglobulin order | Description: Documentation rh-immunoglobulin (rhogam) was not ordered, reason not given |
| G8815 | Doc reas no statin therapy | Description: Documented reason in the medical records for why the statin therapy was not prescribed (i.e., lower extremity bypass was for a patient with non-artherosclerotic disease) |
| G8816 | Statin med pres at disch | Description: Statin medication prescribed at discharge |
| G8817 | Doc reas no statin med disch | Description: Statin therapy not prescribed at discharge, reason not given |
| G8818 | Pt disch to home by day#7 | Description: Patient discharge to home no later than post-operative day #7 |
| G8825 | Pt not disch to home day#7 | Description: Patient not discharged to home by post-operative day #7 |
| G8826 | Pt disch home day #2 evar | Description: Patient discharged to home no later than post-operative day #2 following evar |
| G8833 | Pt not disch home day#2 evar | Description: Patient not discharged to home by post-operative day #2 following evar |
| G8834 | Pt disch home day #2 cea | Description: Patient discharged to home no later than post-operative day #2 following cea |
| G8838 | Not disch home by day #2 | Description: Patient not discharged to home by post-operative day #2 following cea |
| G8839 | Sleep apnea assess | Description: Sleep apnea symptoms assessed, including presence or absence of snoring and daytime sleepiness |
| G8840 | Doc reas no sleep apnea | Description: Documentation of reason(s) for not documenting an assessment of sleep symptoms (e.g., patient didn't have initial daytime sleepiness, patient visited between initial testing and initiation of therapy) |
| G8841 | No sleep apnea assess | Description: Sleep apnea symptoms not assessed, reason not given |
| G8842 | Ahi rdi rei doc win 2mo | Description: Apnea hypopnea index (ahi), respiratory disturbance index (rdi) or respiratory event index (rei) documented or measured within 2 months after initial evaluation for suspected obstructive sleep apnea |
| G8843 | Doc reas no ahi rdi rei | Description: Documentation of reason(s) for not measuring an apnea hypopnea index (ahi), a respiratory disturbance index (rdi), or a respiratory event index (rei) within 2 months after initial evaluation for suspected obstructive sleep apnea (e.g., medical, neurological, or psychiatric disease that prohibits successful completion of a sleep study, patients for whom a sleep study would present a bigger risk than benefit or would pose an undue burden, dementia, patients previously diagnosed with osa and severity assessed by another provider, patients who decline ahi/rdi/rei measurement, patients who had a financial reason for not completing testing, test was ordered but not completed, patients decline because their insurance (payer) does not cover the expense) |
| G8844 | No ahi rdi rei ini dx no rsn | Description: Apnea hypopnea index (ahi), respiratory disturbance index (rdi), or respiratory event index (rei) not documented or measured within 2 months after initial evaluation for suspected obstructive sleep apnea, reason not given |
| G8845 | Pos airway press prescribed | Description: Positive airway pressure therapy prescribed |
| G8846 | Mod or severe osa | Description: Moderate or severe obstructive sleep apnea (apnea hypopnea index (ahi) or respiratory disturbance index (rdi) of 15 or greater) |
| G8848 | Mild osa | Description: Mild obstructive sleep apnea (apnea hypopnea index (ahi) or respiratory disturbance index (rdi) of less than 15) |
| G8849 | Doc reas no pos air press | Description: Documentation of reason(s) for not prescribing positive airway pressure therapy (e.g., patient unable to tolerate, alternative therapies use, patient declined, financial, insurance coverage) |
| G8850 | No pap prescribed | Description: Positive airway pressure therapy not prescribed, reason not given |
| G8851 | Adhere tx assess at lst ann | Description: Adherence to therapy was assessed at least annually through an objective informatics system or through self-reporting (if objective reporting is not available, documented) |
| G8852 | Pos air press prescribe | Description: Positive airway pressure therapy was prescribed |
| G8853 | Pos air press not prescribe | Description: Positive airway pressure therapy not prescribed |
| G8854 | Reas no adhere therapy | Description: Documentation of reason(s) for not objectively reporting adherence to evidence-based therapy (e.g., patients who have been diagnosed with a terminal or advanced disease with an expected life span of less than 6 months, patients who decline therapy, patients who do not return for follow-up at least annually, patients unable to access/afford therapy, patient's insurance will not cover therapy) |
| G8855 | Ther not assessed annually | Description: Adherence to therapy was not assessed at least annually through an objective informatics system or through self-reporting (if objective reporting is not available), reason not given |
| G8856 | Ref for oto eval | Description: Referral to a physician for an otologic evaluation performed |
| G8857 | No elig ref for oto eval | Description: Patient is not eligible for the referral for otologic evaluation measure (e.g., patients who are already under the care of a physician for acute or chronic dizziness) |
| G8858 | Not ref for oto eval | Description: Referral to a physician for an otologic evaluation not performed, reason not given |
| G8859 | Corticosteroids 10mg 60 days | Description: Patient receiving corticosteroids greater than or equal to 10mg/day for 60 or greater consecutive days |
| G8860 | Corticosteroid 10 mg 60 days | Description: Patients who have received dose of corticosteroids greater than or equal to 10mg/day for 60 or greater consecutive days |
| G8861 | Dxa ordered for osteo | Description: Within the past 2 years, central dual-energy x-ray absorptiometry (dxa) ordered and documented, review of systems and medication history or pharmacologic therapy (other than minerals/vitamins) for osteoporosis prescribed |
| G8862 | No corticostrd 10mg 60 days | Description: Patients not receiving corticosteroids greater than or equal to 10mg/day for 60 or greater consecutive days |
| G8863 | No assess bone loss | Description: Patients not assessed for risk of bone loss, reason not given |
| G8864 | Pneumococcal vaccine admin | Description: Pneumococcal vaccine administered or previously received |
| G8865 | Doc med reas no pneumococcal | Description: Documentation of medical reason(s) for not administering or previously receiving pneumococcal vaccine (e.g., patient allergic reaction, potential adverse drug reaction) |
| G8866 | Doc pt reas no pneumococcal | Description: Documentation of patient reason(s) for not administering or previously receiving pneumococcal vaccine (e.g., patient refusal) |
| G8867 | No pneumococcal admin | Description: Pneumococcal vaccine not administered or previously received, reason not given |
| G8868 | 1st course antitnf | Description: Patients receiving a first course of anti-tnf therapy |
| G8869 | Doc immune hep b antitnf | Description: Patient has documented immunity to hepatitis b and initiating anti-tnf therapy |
| G8870 | Hepb admin 1st antitnf | Description: Hepatitis b vaccine injection administered or previously received and is receiving a first course of anti-tnf therapy |
| G8871 | No 1st antitnf | Description: Patient not receiving a first course of anti-tnf therapy |
| G8872 | Intraop image confirm excise | Description: Excised tissue evaluated by imaging intraoperatively to confirm successful inclusion of targeted lesion |
| G8873 | Specimen not intraop image | Description: Patients with needle localization specimens which are not amenable to intraoperative imaging such as mri needle wire localization, or targets which are tentatively identified on mammogram or ultrasound which do not contain a biopsy marker but which can be verified on intraoperative inspection or pathology (e.g., needle biopsy site where the biopsy marker is remote from the actual biopsy site) |
| G8874 | Tissue not image intraop | Description: Excised tissue not evaluated by imaging intraoperatively to confirm successful inclusion of targeted lesion |
| G8875 | Breast cancer dx min invsive | Description: Clinician diagnosed breast cancer preoperatively by a minimally invasive biopsy method |
| G8876 | Doc reas no min inv dx | Description: Documentation of reason(s) for not performing minimally invasive biopsy to diagnose breast cancer preoperatively (e.g., lesion too close to skin, implant, chest wall, etc., lesion could not be adequately visualized for needle biopsy, patient condition prevents needle biopsy [weight, breast thickness, etc.], duct excision without imaging abnormality, prophylactic mastectomy, reduction mammoplasty, excisional biopsy performed by another physician) |
| G8877 | No brst cncr dx min invasive | Description: Clinician did not attempt to achieve the diagnosis of breast cancer preoperatively by a minimally invasive biopsy method, reason not given |
| G8878 | Sent lymph node biopsy | Description: Sentinel lymph node biopsy procedure performed |
| G8879 | Node neg inv brst cncr | Description: Clinically node negative (t1n0m0 or t2n0m0) invasive breast cancer |
| G8880 | Sen lym p node biop not perf | Description: Documentation of reason(s) sentinel lymph node biopsy not performed (e.g., reasons could include but not limited to; non-invasive cancer, incidental discovery of breast cancer on prophylactic mastectomy, incidental discovery of breast cancer on reduction mammoplasty, pre-operative biopsy proven lymph node (ln) metastases, inflammatory carcinoma, stage 3 locally advanced cancer, recurrent invasive breast cancer, clinically node positive after neoadjuvant systemic therapy, patient refusal after informed consent, patient with significant age, comorbidities, or limited life expectancy and favorable tumor; adjuvant systemic therapy unlikely to change) |
| G8881 | Brst cncr stage > t1n0m0 | Description: Stage of breast cancer is greater than t1n0m0 or t2n0m0 |
| G8882 | No sent lymph node biopsy | Description: Sentinel lymph node biopsy procedure not performed, reason not given |
| G8883 | Rev, comm, track, doc biopsy | Description: Biopsy results reviewed, communicated, tracked and documented |
| G8884 | Doc reas biopsy not review | Description: Clinician documented reason that patient's biopsy results were not reviewed |
| G8885 | No rev, comm, track biopsy | Description: Biopsy results not reviewed, communicated, tracked or documented |
| G8886 | Bp under control | Description: Most recent blood pressure under control |
| G8887 | Doc med reas bp not control | Description: Documentation of medical reason(s) for most recent blood pressure not being under control (e.g., patients with palliative goals or for whom treatment of hypertension with standard treatment goals is not clinically appropriate) |
| G8888 | Bp not under control | Description: Most recent blood pressure not under control, results documented and reviewed |
| G8889 | No doc bp | Description: No documentation of blood pressure measurement, reason not given |
| G8890 | Ldl-c under control | Description: Most recent ldl-c under control, results documented and reviewed |
| G8891 | Doc med reas no ldl-c contrl | Description: Documentation of medical reason(s) for most recent ldl-c not under control (e.g., patients with palliative goals for whom treatment of hypertension with standard treatment goals is not clinically appropriate) |
| G8892 | Doc med reas no ldl-c test | Description: Documentation of medical reason(s) for not performing ldl-c test (e.g. patients with palliative goals or for whom treatment of hypertension with standard treatment goals is not clinically appropriate) |
| G8893 | Ldl-c not under control | Description: Most recent ldl-c not under control, results documented and reviewed |
| G8894 | Ldl-c not performed | Description: Ldl-c not performed, reason not given |
| G8895 | Antrom prescribe | Description: Oral aspirin or other antithrombotic therapy prescribed |
| G8896 | Doc med reas no antihtrom | Description: Documentation of medical reason(s) for not prescribing oral aspirin or other antithrombotic therapy (e.g., patient documented to be low risk or patient with terminal illness or treatment of hypertension with standard treatment goals is not clinically appropriate, or for whom risk of aspirin or other antithrombotic therapy exceeds potential benefits such as for individuals whose blood pressure is poorly controlled) |
| G8897 | Antithrom not prescribe | Description: Oral aspirin or other antithrombotic therapy was not prescribed, reason not given |
| G8898 | Copd measures group | Description: I intend to report the chronic obstructive pulmonary disease (copd) measures group |
| G8899 | Inflammatory bowel dis mg | Description: I intend to report the inflammatory bowel disease (ibd) measures group |
| G8900 | Obstructive sleep apnea mg | Description: I intend to report the sleep apnea measures group |
| G8902 | Dementia measures group | Description: I intend to report the dementia measures group |
| G8903 | Parkinson's disease mg | Description: I intend to report the parkinson's disease measures group |
| G8904 | Hypertension mg | Description: I intend to report the hypertension (htn) measures group |
| G8905 | Cardiovascular prevention mg | Description: I intend to report the cardiovascular prevention measures group |
| G8906 | Cataract measures group | Description: I intend to report the cataract measures group |
| G8907 | Pt doc no events on discharg | Description: Patient documented not to have experienced any of the following events: a burn prior to discharge; a fall within the facility; wrong site/side/patient/procedure/implant event; or a hospital transfer or hospital admission upon discharge from the facility |
| G8908 | Pt doc w burn prior to d/c | Description: Patient documented to have received a burn prior to discharge |
| G8909 | Pt doc no burn prior to d/c | Description: Patient documented not to have received a burn prior to discharge |
| G8910 | Pt doc to have fall in asc | Description: Patient documented to have experienced a fall within asc |
| G8911 | Pt doc no fall in asc | Description: Patient documented not to have experienced a fall within ambulatory surgical center |
| G8912 | Pt doc with wrong event | Description: Patient documented to have experienced a wrong site, wrong side, wrong patient, wrong procedure or wrong implant event |
| G8913 | Pt doc no wrong event | Description: Patient documented not to have experienced a wrong site, wrong side, wrong patient, wrong procedure or wrong implant event |
| G8914 | Pt trans to hosp post d/c | Description: Patient documented to have experienced a hospital transfer or hospital admission upon discharge from asc |
| G8915 | Pt not trans to hosp at d/c | Description: Patient documented not to have experienced a hospital transfer or hospital admission upon discharge from asc |
| G8916 | Pt w iv ab given on time | Description: Patient with preoperative order for iv antibiotic surgical site infection (ssi) prophylaxis, antibiotic initiated on time |
| G8917 | Pt w iv ab not given on time | Description: Patient with preoperative order for iv antibiotic surgical site infection (ssi) prophylaxis, antibiotic not initiated on time |
| G8918 | Pt w/o preop order iv ab pro | Description: Patient without preoperative order for iv antibiotic surgical site infection (ssi) prophylaxis |
| G8923 | Lvef <= 40% or lvsd | Description: Current or prior left ventricular ejection fraction (lvef) <= 40% or documentation of moderately or severely depressed left ventricular systolic function |
| G8924 | Spir res doc fev1/fvc<70% | Description: Spirometry results documented (fev1/fvc < 70%) |
| G8925 | Spir fev1/fvc>=60% & no copd | Description: Spirometry test results demonstrate fev1 >= 60% fev1/fvc >= 70%, predicted or patient does not have copd symptoms |
| G8926 | Spiro no perf or doc | Description: Spirometry test not performed or documented, reason not given |
| G8927 | Adj chem pres ajcc iii | Description: Adjuvant chemotherapy referred, prescribed or previously received for ajcc stage iii, colon cancer |
| G8928 | Adj chem not pres rsn spec | Description: Adjuvant chemotherapy not prescribed or previously received, for documented reasons (e.g., medical co-morbidities, diagnosis date more than 5 years prior to the current visit date, patient's diagnosis date is within 120 days of the end of the 12 month reporting period, patient's cancer has metastasized, medical contraindication/allergy, poor performance status, other medical reasons, patient refusal, other patient reasons, patient is currently enrolled in a clinical trial that precludes prescription of chemotherapy, other system reasons) |
| G8929 | Adj cmo not pres rsn not gvn | Description: Adjuvant chemotherapy not prescribed or previously received, reason not given |
| G8930 | Assess of dep @ initial eval | Description: Assessment of depression severity at the initial evaluation |
| G8931 | Asses of dep not documented | Description: Assessment of depression severity not documented, reason not given |
| G8932 | Suicd rsk assessed init eval | Description: Suicide risk assessed at the initial evaluation |
| G8933 | Suicide risk not assessed | Description: Suicide risk not assessed at the initial evaluation, reason not given |
| G8934 | Lvef <=40% or dep lv sys fcn | Description: Current or prior left ventricular ejection fraction (lvef) <=40% or documentation of moderately or severely depressed left ventricular systolic function |
| G8935 | Rx ace or arb therapy | Description: Clinician prescribed angiotensin converting enzyme (ace) inhibitor or angiotensin receptor blocker (arb) therapy |
| G8936 | Pt not eligible ace/arb | Description: Clinician documented that patient was not an eligible candidate for angiotensin converting enzyme (ace) inhibitor or angiotensin receptor blocker (arb) therapy (eg, allergy, intolerance, pregnancy, renal failure due to ace inhibitor, diseases of the aortic or mitral valve, other medical reasons) or (eg, patient declined, other patient reasons) |
| G8937 | No rx ace/arb therapy | Description: Clinician did not prescribe angiotensin converting enzyme (ace) inhibitor or angiotensin receptor blocker (arb) therapy, reason not given |
| G8938 | Bmi doc onl fup nt doc | Description: Bmi is documented as being outside of normal parameters, follow-up plan is not documented, documentation the patient is not eligible |
| G8939 | Pain as doc positive, no f/u | Description: Pain assessment documented as positive, follow-up plan not documented, documentation the patient is not eligible at the time of the encounter |
| G8940 | Scr dep pos, no plan done | Description: Screening for depression documented as positive, a follow-up plan not completed, documented reason |
| G8941 | Eld maltreatment doc as pos | Description: Elder maltreatment screen documented as positive, follow-up plan not documented, documentation the patient is not eligible for follow-up plan at the time of the encounter |
| G8942 | Doc fcn/care plan w/30 days | Description: Functional outcome assessment using a standardized tool is documented within the previous 30 days and a care plan, based on identified deficiencies is documented within two days of the functional outcome assessment |
| G8943 | Ldlc not pres w/i 12 mo prir | Description: Ldl-c result not present or not within 12 months prior |
| G8944 | Ajcc mel cnr stg 0 - iic | Description: Ajcc melanoma cancer stage 0 through iic melanoma |
| G8946 | Mibm but no dx of breast ca | Description: Minimally invasive biopsy method attempted but not diagnostic of breast cancer (e.g., high risk lesion of breast such as atypical ductal hyperplasia, lobular neoplasia, atypical lobular hyperplasia, lobular carcinoma in situ, atypical columnar hyperplasia, flat epithelial atypia, radial scar, complex sclerosing lesion, papillary lesion, or any lesion with spindle cells) |
| G8947 | 1 or more neuropsych | Description: One or more neuropsychiatric symptoms |
| G8948 | No neuropsych symptoms | Description: No neuropsychiatric symptoms |
| G8949 | Doc pt reas on counsel diet | Description: Documentation of patient reason(s) for patient not receiving counseling for diet and physical activity (e.g., patient is not willing to discuss diet or exercise interventions to help control blood pressure, or the patient said he/she refused to make these changes) |
| G8950 | Pre-htn or htn doc, f/u indc | Description: Elevated or hypertensive blood pressure reading documented, and the indicated follow-up is documented |
| G8951 | Pre-htn/htn doc, no pt f/u | Description: Pre-hypertensive or hypertensive blood pressure reading documented, indicated follow-up not documented, documentation the patient is not eligible |
| G8952 | Pre-htn/htn, no f/u, not gvn | Description: Elevated or hypertensive blood pressure reading documented, indicated follow-up not documented, reason not given |
| G8953 | Oncology mg qual act perform | Description: All quality actions for the applicable measures in the oncology measures group have been performed for this patient |
| G8955 | Most recent assess vol mgmt | Description: Most recent assessment of adequacy of volume management documented |
| G8956 | Pt rcv hedia outpt dyls fac | Description: Patient receiving maintenance hemodialysis in an outpatient dialysis facility |
| G8957 | Pt no hedia in outpt fac | Description: Patient not receiving maintenance hemodialysis in an outpatient dialysis facility |
| G8958 | Assess vol mgmt not doc | Description: Assessment of adequacy of volume management not documented, reason not given |
| G8959 | Clin tx mdd comm to tx clin | Description: Clinician treating major depressive disorder communicates to clinician treating comorbid condition |
| G8960 | Clin tx mdd not comm | Description: Clinician treating major depressive disorder did not communicate to clinician treating comorbid condition, reason not given |
| G8961 | Csit lowrisk surg pts preop | Description: Cardiac stress imaging test primarily performed on low-risk surgery patient for preoperative evaluation within 30 days preceding this surgery |
| G8962 | Csit on pt any reas 30 days | Description: Cardiac stress imaging test performed on patient for any reason including those who did not have low risk surgery or test that was performed more than 30 days preceding low risk surgery |
| G8963 | Csi per asx pt w/pci 2 yrs | Description: Cardiac stress imaging performed primarily for monitoring of asymptomatic patient who had pci within 2 years |
| G8964 | Csi any other than pci 2 yr | Description: Cardiac stress imaging test performed primarily for any other reason than monitoring of asymptomatic patient who had pci within 2 years (e.g., symptomatic patient, patient greater than 2 years since pci, initial evaluation, etc) |
| G8965 | Csit perf on low chd rsk | Description: Cardiac stress imaging test primarily performed on low chd risk patient for initial detection and risk assessment |
| G8966 | Csit perf sx or high chd rsk | Description: Cardiac stress imaging test performed on symptomatic or higher than low chd risk patient or for any reason other than initial detection and risk assessment |
| G8967 | Warf or other fda drug presc | Description: Fda approved oral anticoagulant is prescribed |
| G8968 | Doc med not presb | Description: Documentation of medical reason(s) for not prescribing an fda-approved anticoagulant (e.g., present or planned atrial appendage occlusion or ligation or patient being currently enrolled in a clinical trial related to af/atrial flutter treatment) |
| G8969 | Doc pt rsn no presc warf/fda | Description: Documentation of patient reason(s) for not prescribing an oral anticoagulant that is fda approved for the prevention of thromboembolism (e.g., patient preference for not receiving anticoagulation) |
| G8970 | No rsk fac or 1 mod risk te | Description: No risk factors or one moderate risk factor for thromboembolism |
| G8971 | Warfrn or othr antcog no rx | Description: Warfarin or another oral anticoagulant that is fda approved not prescribed, reason not given |
| G8972 | 1>=risk or>= mod risk for te | Description: One or more high risk factors for thromboembolism or more than one moderate risk factor for thromboembolism |
| G8973 | Mst rcnt hbb < 10g/dl | Description: Most recent hemoglobin (hgb) level < 10 g/dl |
| G8974 | Hgb not doc rns not gvn | Description: Hemoglobin level measurement not documented, reason not given |
| G8975 | Hgb <10g/dl, med rsn | Description: Documentation of medical reason(s) for patient having a hemoglobin level < 10 g/dl (e.g., patients who have non-renal etiologies of anemia [e.g., sickle cell anemia or other hemoglobinopathies, hypersplenism, primary bone marrow disease, anemia related to chemotherapy for diagnosis of malignancy, postoperative bleeding, active bloodstream or peritoneal infection], other medical reasons) |
| G8976 | Hgb >= 10 g/dl | Description: Most recent hemoglobin (hgb) level >= 10 g/dl |
| G8977 | Oncology measures grp | Description: I intend to report the oncology measures group |
| G8978 | Mobility current status | Description: Mobility: walking & moving around functional limitation, current status, at therapy episode outset and at reporting intervals |
| G8979 | Mobility goal status | Description: Mobility: walking & moving around functional limitation, projected goal status, at therapy episode outset, at reporting intervals, and at discharge or to end reporting |
| G8980 | Mobility d/c status | Description: Mobility: walking & moving around functional limitation, discharge status, at discharge from therapy or to end reporting |
| G8981 | Body pos current status | Description: Changing & maintaining body position functional limitation, current status, at therapy episode outset and at reporting intervals |
| G8982 | Body pos goal status | Description: Changing & maintaining body position functional limitation, projected goal status, at therapy episode outset, at reporting intervals, and at discharge or to end reporting |
| G8983 | Body pos d/c status | Description: Changing & maintaining body position functional limitation, discharge status, at discharge from therapy or to end reporting |
| G8984 | Carry current status | Description: Carrying, moving & handling objects functional limitation, current status, at therapy episode outset and at reporting intervals |
| G8985 | Carry goal status | Description: Carrying, moving and handling objects, projected goal status, at therapy episode outset, at reporting intervals, and at discharge or to end reporting |
| G8986 | Carry d/c status | Description: Carrying, moving & handling objects functional limitation, discharge status, at discharge from therapy or to end reporting |
| G8987 | Self care current status | Description: Self care functional limitation, current status, at therapy episode outset and at reporting intervals |
| G8988 | Self care goal status | Description: Self care functional limitation, projected goal status, at therapy episode outset, at reporting intervals, and at discharge or to end reporting |
| G8989 | Self care d/c status | Description: Self care functional limitation, discharge status, at discharge from therapy or to end reporting |
| G8990 | Other pt/ot current status | Description: Other physical or occupational therapy primary functional limitation, current status, at therapy episode outset and at reporting intervals |
| G8991 | Other pt/ot goal status | Description: Other physical or occupational therapy primary functional limitation, projected goal status, at therapy episode outset, at reporting intervals, and at discharge or to end reporting |
| G8992 | Other pt/ot d/c status | Description: Other physical or occupational therapy primary functional limitation, discharge status, at discharge from therapy or to end reporting |
| G8993 | Sub pt/ot current status | Description: Other physical or occupational therapy subsequent functional limitation, current status, at therapy episode outset and at reporting intervals |
| G8994 | Sub pt/ot goal status | Description: Other physical or occupational therapy subsequent functional limitation, projected goal status, at therapy episode outset, at reporting intervals, and at discharge or to end reporting |
| G8995 | Sub pt/ot d/c status | Description: Other physical or occupational therapy subsequent functional limitation, discharge status, at discharge from therapy or to end reporting |
| G8996 | Swallow current status | Description: Swallowing functional limitation, current status at therapy episode outset and at reporting intervals |
| G8997 | Swallow goal status | Description: Swallowing functional limitation, projected goal status, at therapy episode outset, at reporting intervals, and at discharge or to end reporting |
| G8998 | Swallow d/c status | Description: Swallowing functional limitation, discharge status, at discharge from therapy or to end reporting |
| G8999 | Motor speech current status | Description: Motor speech functional limitation, current status at therapy episode outset and at reporting intervals |
| G9001 | Mccd, initial rate | Description: Coordinated care fee, initial rate |
| G9002 | Mccd,maintenance rate | Description: Coordinated care fee, maintenance rate |
| G9003 | Mccd, risk adj hi, initial | Description: Coordinated care fee, risk adjusted high, initial |
| G9004 | Mccd, risk adj lo, initial | Description: Coordinated care fee, risk adjusted low, initial |
| G9005 | Mccd, risk adj, maintenance | Description: Coordinated care fee, risk adjusted maintenance |
| G9006 | Mccd, home monitoring | Description: Coordinated care fee, home monitoring |
| G9007 | Mccd, sch team conf | Description: Coordinated care fee, scheduled team conference |
| G9008 | Mccd,phys coor-care ovrsght | Description: Coordinated care fee, physician coordinated care oversight services |
| G9009 | Mccd, risk adj, level 3 | Description: Coordinated care fee, risk adjusted maintenance, level 3 |
| G9010 | Mccd, risk adj, level 4 | Description: Coordinated care fee, risk adjusted maintenance, level 4 |
| G9011 | Mccd, risk adj, level 5 | Description: Coordinated care fee, risk adjusted maintenance, level 5 |
| G9012 | Other specified case mgmt | Description: Other specified case management service not elsewhere classified |
| G9013 | Esrd demo bundle level i | Description: Esrd demo basic bundle level i |
| G9014 | Esrd demo bundle-level ii | Description: Esrd demo expanded bundle including venous access and related services |
| G9016 | Demo-smoking cessation coun | Description: Smoking cessation counseling, individual, in the absence of or in addition to any other evaluation and management service, per session (6-10 minutes) [demo project code only] |
| G9017 | Amantadine hcl 100mg oral | Description: Amantadine hydrochloride, oral, per 100 mg (for use in a medicare-approved demonstration project) |
| G9018 | Zanamivir,inhalation pwd 10m | Description: Zanamivir, inhalation powder, administered through inhaler, per 10 mg (for use in a medicare-approved demonstration project) |
| G9019 | Oseltamivir phosphate 75mg | Description: Oseltamivir phosphate, oral, per 75 mg (for use in a medicare-approved demonstration project) |
| G9020 | Rimantadine hcl 100mg oral | Description: Rimantadine hydrochloride, oral, per 100 mg (for use in a medicare-approved demonstration project) |
| G9033 | Amantadine hcl oral brand | Description: Amantadine hydrochloride, oral brand, per 100 mg (for use in a medicare-approved demonstration project) |
| G9034 | Zanamivir, inh pwdr, brand | Description: Zanamivir, inhalation powder, administered through inhaler, brand, per 10 mg (for use in a medicare-approved demonstration project) |
| G9035 | Oseltamivir phosp, brand | Description: Oseltamivir phosphate, oral, brand, per 75 mg (for use in a medicare-approved demonstration project) |
| G9036 | Rimantadine hcl, brand | Description: Rimantadine hydrochloride, oral, brand, per 100 mg (for use in a medicare-approved demonstration project) |
| G9037 | Intrpro req fr rec phys/qhcp | Description: Interprofessional telephone/internet/electronic health record clinical question/request for specialty recommendations by a treating/requesting physician or other qualified health care professional for the care of the patient (i.e. not for professional education or scheduling) and may include subsequent follow up on the specialist's recommendations; 30 minutes |
| G9038 | Co-management services | Description: Co-management services with the following elements: new diagnosis or acute exacerbation and stabilization of existing condition; condition which may benefit from joint care planning; condition for which specialist is taking a co-management role; condition expected to last at least 3 months; comprehensive care plan established, implemented, revised or monitored in partnership with co-managing clinicians; ongoing communication and care coordination between co-managing clinicians furnishing care |
| G9050 | Oncology work-up evaluation | Description: Oncology; primary focus of visit; work-up, evaluation, or staging at the time of cancer diagnosis or recurrence (for use in a medicare-approved demonstration project) |
| G9051 | Oncology tx decision-mgmt | Description: Oncology; primary focus of visit; treatment decision-making after disease is staged or restaged, discussion of treatment options, supervising/coordinating active cancer directed therapy or managing consequences of cancer directed therapy (for use in a medicare-approved demonstration project) |
| G9052 | Onc surveillance for disease | Description: Oncology; primary focus of visit; surveillance for disease recurrence for patient who has completed definitive cancer-directed therapy and currently lacks evidence of recurrent disease; cancer directed therapy might be considered in the future (for use in a medicare-approved demonstration project) |
| G9053 | Onc expectant management pt | Description: Oncology; primary focus of visit; expectant management of patient with evidence of cancer for whom no cancer directed therapy is being administered or arranged at present; cancer directed therapy might be considered in the future (for use in a medicare-approved demonstration project) |
| G9054 | Onc supervision palliative | Description: Oncology; primary focus of visit; supervising, coordinating or managing care of patient with terminal cancer or for whom other medical illness prevents further cancer treatment; includes symptom management, end-of-life care planning, management of palliative therapies (for use in a medicare-approved demonstration project) |
| G9055 | Onc visit unspecified nos | Description: Oncology; primary focus of visit; other, unspecified service not otherwise listed (for use in a medicare-approved demonstration project) |
| G9056 | Onc prac mgmt adheres guide | Description: Oncology; practice guidelines; management adheres to guidelines (for use in a medicare-approved demonstration project) |
| G9057 | Onc pract mgmt differs trial | Description: Oncology; practice guidelines; management differs from guidelines as a result of patient enrollment in an institutional review board approved clinical trial (for use in a medicare-approved demonstration project) |
| G9058 | Onc prac mgmt disagree w/gui | Description: Oncology; practice guidelines; management differs from guidelines because the treating physician disagrees with guideline recommendations (for use in a medicare-approved demonstration project) |
| G9059 | Onc prac mgmt pt opt alterna | Description: Oncology; practice guidelines; management differs from guidelines because the patient, after being offered treatment consistent with guidelines, has opted for alternative treatment or management, including no treatment (for use in a medicare-approved demonstration project) |
| G9060 | Onc prac mgmt dif pt comorb | Description: Oncology; practice guidelines; management differs from guidelines for reason(s) associated with patient comorbid illness or performance status not factored into guidelines (for use in a medicare-approved demonstration project) |
| G9061 | Onc prac cond noadd by guide | Description: Oncology; practice guidelines; patient's condition not addressed by available guidelines (for use in a medicare-approved demonstration project) |
| G9062 | Onc prac guide differs nos | Description: Oncology; practice guidelines; management differs from guidelines for other reason(s) not listed (for use in a medicare-approved demonstration project) |
| G9063 | Onc dx nsclc stgi no progres | Description: Oncology; disease status; limited to non-small cell lung cancer; extent of disease initially established as stage i (prior to neo-adjuvant therapy, if any) with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) |
| G9064 | Onc dx nsclc stg2 no progres | Description: Oncology; disease status; limited to non-small cell lung cancer; extent of disease initially established as stage ii (prior to neo-adjuvant therapy, if any) with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) |
| G9065 | Onc dx nsclc stg3a no progre | Description: Oncology; disease status; limited to non-small cell lung cancer; extent of disease initially established as stage iii a (prior to neo-adjuvant therapy, if any) with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) |
| G9066 | Onc dx nsclc stg3b-4 metasta | Description: Oncology; disease status; limited to non-small cell lung cancer; stage iii b- iv at diagnosis, metastatic, locally recurrent, or progressive (for use in a medicare-approved demonstration project) |
| G9067 | Onc dx nsclc dx unknown nos | Description: Oncology; disease status; limited to non-small cell lung cancer; extent of disease unknown, staging in progress, or not listed (for use in a medicare-approved demonstration project) |
| G9068 | Onc dx sclc/nsclc limited | Description: Oncology; disease status; limited to small cell and combined small cell/non-small cell; extent of disease initially established as limited with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) |
| G9069 | Onc dx sclc/nsclc ext at dx | Description: Oncology; disease status; small cell lung cancer, limited to small cell and combined small cell/non-small cell; extensive stage at diagnosis, metastatic, locally recurrent, or progressive (for use in a medicare-approved demonstration project) |
| G9070 | Onc dx sclc/nsclc ext unknwn | Description: Oncology; disease status; small cell lung cancer, limited to small cell and combined small cell/non-small; extent of disease unknown, staging in progress, or not listed (for use in a medicare-approved demonstration project) |
| G9071 | Onc dx brst stg1-2b hr,nopro | Description: Oncology; disease status; invasive female breast cancer (does not include ductal carcinoma in situ); adenocarcinoma as predominant cell type; stage i or stage iia-iib; or t3, n1, m0; and er and/or pr positive; with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) |
| G9072 | Onc dx brst stg1-2 noprogres | Description: Oncology; disease status; invasive female breast cancer (does not include ductal carcinoma in situ); adenocarcinoma as predominant cell type; stage i, or stage iia-iib; or t3, n1, m0; and er and pr negative; with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) |
| G9073 | Onc dx brst stg3-hr, no pro | Description: Oncology; disease status; invasive female breast cancer (does not include ductal carcinoma in situ); adenocarcinoma as predominant cell type; stage iiia-iiib; and not t3, n1, m0; and er and/or pr positive; with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) |
| G9074 | Onc dx brst stg3-noprogress | Description: Oncology; disease status; invasive female breast cancer (does not include ductal carcinoma in situ); adenocarcinoma as predominant cell type; stage iiia-iiib; and not t3, n1, m0; and er and pr negative; with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) |
| G9075 | Onc dx brst metastic/ recur | Description: Oncology; disease status; invasive female breast cancer (does not include ductal carcinoma in situ); adenocarcinoma as predominant cell type; m1 at diagnosis, metastatic, locally recurrent, or progressive (for use in a medicare-approved demonstration project) |
| G9077 | Onc dx prostate t1no progres | Description: Oncology; disease status; prostate cancer, limited to adenocarcinoma as predominant cell type; t1-t2c and gleason 2-7 and psa < or equal to 20 at diagnosis with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) |
| G9078 | Onc dx prostate t2no progres | Description: Oncology; disease status; prostate cancer, limited to adenocarcinoma as predominant cell type; t2 or t3a gleason 8-10 or psa > 20 at diagnosis with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) |
| G9079 | Onc dx prostate t3b-t4noprog | Description: Oncology; disease status; prostate cancer, limited to adenocarcinoma as predominant cell type; t3b-t4, any n; any t, n1 at diagnosis with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) |
| G9080 | Onc dx prostate w/rise psa | Description: Oncology; disease status; prostate cancer, limited to adenocarcinoma; after initial treatment with rising psa or failure of psa decline (for use in a medicare-approved demonstration project) |
| G9083 | Onc dx prostate unknwn nos | Description: Oncology; disease status; prostate cancer, limited to adenocarcinoma; extent of disease unknown, staging in progress, or not listed (for use in a medicare-approved demonstration project) |
| G9084 | Onc dx colon t1-3,n1-2,no pr | Description: Oncology; disease status; colon cancer, limited to invasive cancer, adenocarcinoma as predominant cell type; extent of disease initially established as t1-3, n0, m0 with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) |
| G9085 | Onc dx colon t4, n0 w/o prog | Description: Oncology; disease status; colon cancer, limited to invasive cancer, adenocarcinoma as predominant cell type; extent of disease initially established as t4, n0, m0 with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) |
| G9086 | Onc dx colon t1-4 no dx prog | Description: Oncology; disease status; colon cancer, limited to invasive cancer, adenocarcinoma as predominant cell type; extent of disease initially established as t1-4, n1-2, m0 with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) |
| G9087 | Onc dx colon metas evid dx | Description: Oncology; disease status; colon cancer, limited to invasive cancer, adenocarcinoma as predominant cell type; m1 at diagnosis, metastatic, locally recurrent, or progressive with current clinical, radiologic, or biochemical evidence of disease (for use in a medicare-approved demonstration project) |
| G9088 | Onc dx colon metas noevid dx | Description: Oncology; disease status; colon cancer, limited to invasive cancer, adenocarcinoma as predominant cell type; m1 at diagnosis, metastatic, locally recurrent, or progressive without current clinical, radiologic, or biochemical evidence of disease (for use in a medicare-approved demonstration project) |
| G9089 | Onc dx colon extent unknown | Description: Oncology; disease status; colon cancer, limited to invasive cancer, adenocarcinoma as predominant cell type; extent of disease unknown, staging in progress, or not listed (for use in a medicare-approved demonstration project) |
| G9090 | Onc dx rectal t1-2 no progr | Description: Oncology; disease status; rectal cancer, limited to invasive cancer, adenocarcinoma as predominant cell type; extent of disease initially established as t1-2, n0, m0 (prior to neo-adjuvant therapy, if any) with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) |
| G9091 | Onc dx rectal t3 n0 no prog | Description: Oncology; disease status; rectal cancer, limited to invasive cancer, adenocarcinoma as predominant cell type; extent of disease initially established as t3, n0, m0 (prior to neo-adjuvant therapy, if any) with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) |
| G9092 | Onc dx rectal t1-3,n1-2noprg | Description: Oncology; disease status; rectal cancer, limited to invasive cancer, adenocarcinoma as predominant cell type; extent of disease initially established as t1-3, n1-2, m0 (prior to neo-adjuvant therapy, if any) with no evidence of disease progression, recurrence or metastases (for use in a medicare-approved demonstration project) |
| G9093 | Onc dx rectal t4,n,m0 no prg | Description: Oncology; disease status; rectal cancer, limited to invasive cancer, adenocarcinoma as predominant cell type; extent of disease initially established as t4, any n, m0 (prior to neo-adjuvant therapy, if any) with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) |
| G9094 | Onc dx rectal m1 w/mets prog | Description: Oncology; disease status; rectal cancer, limited to invasive cancer, adenocarcinoma as predominant cell type; m1 at diagnosis, metastatic, locally recurrent, or progressive (for use in a medicare-approved demonstration project) |
| G9095 | Onc dx rectal extent unknwn | Description: Oncology; disease status; rectal cancer, limited to invasive cancer, adenocarcinoma as predominant cell type; extent of disease unknown, staging in progress, or not listed (for use in a medicare-approved demonstration project) |
| G9096 | Onc dx esophag t1-t3 noprog | Description: Oncology; disease status; esophageal cancer, limited to adenocarcinoma or squamous cell carcinoma as predominant cell type; extent of disease initially established as t1-t3, n0-n1 or nx (prior to neo-adjuvant therapy, if any) with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) |
| G9097 | Onc dx esophageal t4 no prog | Description: Oncology; disease status; esophageal cancer, limited to adenocarcinoma or squamous cell carcinoma as predominant cell type; extent of disease initially established as t4, any n, m0 (prior to neo-adjuvant therapy, if any) with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) |
| G9098 | Onc dx esophageal mets recur | Description: Oncology; disease status; esophageal cancer, limited to adenocarcinoma or squamous cell carcinoma as predominant cell type; m1 at diagnosis, metastatic, locally recurrent, or progressive (for use in a medicare-approved demonstration project) |
| G9099 | Onc dx esophageal unknown | Description: Oncology; disease status; esophageal cancer, limited to adenocarcinoma or squamous cell carcinoma as predominant cell type; extent of disease unknown, staging in progress, or not listed (for use in a medicare-approved demonstration project) |
| G9100 | Onc dx gastric no recurrence | Description: Oncology; disease status; gastric cancer, limited to adenocarcinoma as predominant cell type; post r0 resection (with or without neoadjuvant therapy) with no evidence of disease recurrence, progression, or metastases (for use in a medicare-approved demonstration project) |
| G9101 | Onc dx gastric p r1-r2noprog | Description: Oncology; disease status; gastric cancer, limited to adenocarcinoma as predominant cell type; post r1 or r2 resection (with or without neoadjuvant therapy) with no evidence of disease progression, or metastases (for use in a medicare-approved demonstration project) |
| G9102 | Onc dx gastric unresectable | Description: Oncology; disease status; gastric cancer, limited to adenocarcinoma as predominant cell type; clinical or pathologic m0, unresectable with no evidence of disease progression, or metastases (for use in a medicare-approved demonstration project) |
| G9103 | Onc dx gastric recurrent | Description: Oncology; disease status; gastric cancer, limited to adenocarcinoma as predominant cell type; clinical or pathologic m1 at diagnosis, metastatic, locally recurrent, or progressive (for use in a medicare-approved demonstration project) |
| G9104 | Onc dx gastric unknown nos | Description: Oncology; disease status; gastric cancer, limited to adenocarcinoma as predominant cell type; extent of disease unknown, staging in progress, or not listed (for use in a medicare-approved demonstration project) |
| G9105 | Onc dx pancreatc p r0 res no | Description: Oncology; disease status; pancreatic cancer, limited to adenocarcinoma as predominant cell type; post r0 resection without evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) |
| G9106 | Onc dx pancreatc p r1/r2 no | Description: Oncology; disease status; pancreatic cancer, limited to adenocarcinoma; post r1 or r2 resection with no evidence of disease progression, or metastases (for use in a medicare-approved demonstration project) |
| G9107 | Onc dx pancreatic unresectab | Description: Oncology; disease status; pancreatic cancer, limited to adenocarcinoma; unresectable at diagnosis, m1 at diagnosis, metastatic, locally recurrent, or progressive (for use in a medicare-approved demonstration project) |
| G9108 | Onc dx pancreatic unknwn nos | Description: Oncology; disease status; pancreatic cancer, limited to adenocarcinoma; extent of disease unknown, staging in progress, or not listed (for use in a medicare-approved demonstration project) |
| G9109 | Onc dx head/neck t1-t2no prg | Description: Oncology; disease status; head and neck cancer, limited to cancers of oral cavity, pharynx and larynx with squamous cell as predominant cell type; extent of disease initially established as t1-t2 and n0, m0 (prior to neo-adjuvant therapy, if any) with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) |
| G9110 | Onc dx head/neck t3-4 noprog | Description: Oncology; disease status; head and neck cancer, limited to cancers of oral cavity, pharynx and larynx with squamous cell as predominant cell type; extent of disease initially established as t3-4 and/or n1-3, m0 (prior to neo-adjuvant therapy, if any) with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) |
| G9111 | Onc dx head/neck m1 mets rec | Description: Oncology; disease status; head and neck cancer, limited to cancers of oral cavity, pharynx and larynx with squamous cell as predominant cell type; m1 at diagnosis, metastatic, locally recurrent, or progressive (for use in a medicare-approved demonstration project) |
| G9112 | Onc dx head/neck ext unknown | Description: Oncology; disease status; head and neck cancer, limited to cancers of oral cavity, pharynx and larynx with squamous cell as predominant cell type; extent of disease unknown, staging in progress, or not listed (for use in a medicare-approved demonstration project) |
| G9113 | Onc dx ovarian stg1a-b no pr | Description: Oncology; disease status; ovarian cancer, limited to epithelial cancer; pathologic stage ia-b (grade 1) without evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) |
| G9114 | Onc dx ovarian stg1a-b or 2 | Description: Oncology; disease status; ovarian cancer, limited to epithelial cancer; pathologic stage ia-b (grade 2-3); or stage ic (all grades); or stage ii; without evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) |
| G9115 | Onc dx ovarian stg3/4 noprog | Description: Oncology; disease status; ovarian cancer, limited to epithelial cancer; pathologic stage iii-iv; without evidence of progression, recurrence, or metastases (for use in a medicare-approved demonstration project) |
| G9116 | Onc dx ovarian recurrence | Description: Oncology; disease status; ovarian cancer, limited to epithelial cancer; evidence of disease progression, or recurrence, and/or platinum resistance (for use in a medicare-approved demonstration project) |
| G9117 | Onc dx ovarian unknown nos | Description: Oncology; disease status; ovarian cancer, limited to epithelial cancer; extent of disease unknown, staging in progress, or not listed (for use in a medicare-approved demonstration project) |
| G9123 | Onc dx cml chronic phase | Description: Oncology; disease status; chronic myelogenous leukemia, limited to philadelphia chromosome positive and/or bcr-abl positive; chronic phase not in hematologic, cytogenetic, or molecular remission (for use in a medicare-approved demonstration project) |
| G9124 | Onc dx cml acceler phase | Description: Oncology; disease status; chronic myelogenous leukemia, limited to philadelphia chromosome positive and/or bcr-abl positive; accelerated phase not in hematologic cytogenetic, or molecular remission (for use in a medicare-approved demonstration project) |
| G9125 | Onc dx cml blast phase | Description: Oncology; disease status; chronic myelogenous leukemia, limited to philadelphia chromosome positive and/or bcr-abl positive; blast phase not in hematologic, cytogenetic, or molecular remission (for use in a medicare-approved demonstration project) |
| G9126 | Onc dx cml remission | Description: Oncology; disease status; chronic myelogenous leukemia, limited to philadelphia chromosome positive and/or bcr-abl positive; in hematologic, cytogenetic, or molecular remission (for use in a medicare-approved demonstration project) |
| G9128 | Onc dx multi myeloma stage i | Description: Oncology; disease status; limited to multiple myeloma, systemic disease; smoldering, stage i (for use in a medicare-approved demonstration project) |
| G9129 | Onc dx mult myeloma stg2 hig | Description: Oncology; disease status; limited to multiple myeloma, systemic disease; stage ii or higher (for use in a medicare-approved demonstration project) |
| G9130 | Onc dx multi myeloma unknown | Description: Oncology; disease status; limited to multiple myeloma, systemic disease; extent of disease unknown, staging in progress, or not listed (for use in a medicare-approved demonstration project) |
| G9131 | Onc dx brst unknown nos | Description: Oncology; disease status; invasive female breast cancer (does not include ductal carcinoma in situ); adenocarcinoma as predominant cell type; extent of disease unknown, staging in progress, or not listed (for use in a medicare-approved demonstration project) |
| G9132 | Onc dx prostate mets no cast | Description: Oncology; disease status; prostate cancer, limited to adenocarcinoma; hormone-refractory/androgen-independent (e.g., rising psa on anti-androgen therapy or post-orchiectomy); clinical metastases (for use in a medicare-approved demonstration project) |
| G9133 | Onc dx prostate clinical met | Description: Oncology; disease status; prostate cancer, limited to adenocarcinoma; hormone-responsive; clinical metastases or m1 at diagnosis (for use in a medicare-approved demonstration project) |
| G9134 | Onc nhlstg 1-2 no relap no | Description: Oncology; disease status; non-hodgkin's lymphoma, any cellular classification; stage i, ii at diagnosis, not relapsed, not refractory (for use in a medicare-approved demonstration project) |
| G9135 | Onc dx nhl stg 3-4 not relap | Description: Oncology; disease status; non-hodgkin's lymphoma, any cellular classification; stage iii, iv, not relapsed, not refractory (for use in a medicare-approved demonstration project) |
| G9136 | Onc dx nhl trans to lg bcell | Description: Oncology; disease status; non-hodgkin's lymphoma, transformed from original cellular diagnosis to a second cellular classification (for use in a medicare-approved demonstration project) |
| G9137 | Onc dx nhl relapse/refractor | Description: Oncology; disease status; non-hodgkin's lymphoma, any cellular classification; relapsed/refractory (for use in a medicare-approved demonstration project) |
| G9138 | Onc dx nhl stg unknown | Description: Oncology; disease status; non-hodgkin's lymphoma, any cellular classification; diagnostic evaluation, stage not determined, evaluation of possible relapse or non-response to therapy, or not listed (for use in a medicare-approved demonstration project) |
| G9139 | Onc dx cml dx status unknown | Description: Oncology; disease status; chronic myelogenous leukemia, limited to philadelphia chromosome positive and/or bcr-abl positive; extent of disease unknown, staging in progress, not listed (for use in a medicare-approved demonstration project) |
| G9140 | Frontier extended stay demo | Description: Frontier extended stay clinic demonstration; for a patient stay in a clinic approved for the cms demonstration project; the following measures should be present: the stay must be equal to or greater than 4 hours; weather or other conditions must prevent transfer or the case falls into a category of monitoring and observation cases that are permitted by the rules of the demonstration; there is a maximum frontier extended stay clinic (fesc) visit of 48 hours, except in the case when weather or other conditions prevent transfer; payment is made on each period up to 4 hours, after the first 4 hours |
| G9143 | Warfarin respon genetic test | Description: Warfarin responsiveness testing by genetic technique using any method, any number of specimen(s) |
| G9147 | Outpt iv insulin tx any mea | Description: Outpatient intravenous insulin treatment (oivit) either pulsatile or continuous, by any means, guided by the results of measurements for: respiratory quotient; and/or, urine urea nitrogen (uun); and/or, arterial, venous or capillary glucose; and/or potassium concentration |
| G9148 | Medical home level 1 | Description: National committee for quality assurance - level 1 medical home |
| G9149 | Medical home level ii | Description: National committee for quality assurance - level 2 medical home |
| G9150 | Medical home level iii | Description: National committee for quality assurance - level 3 medical home |
| G9151 | Mapcp demo state | Description: Mapcp demonstration - state provided services |
| G9152 | Mapcp demo community | Description: Mapcp demonstration - community health teams |
| G9153 | Mapcp demo physician | Description: Mapcp demonstration - physician incentive pool |
| G9156 | Evaluation for wheelchair | Description: Evaluation for wheelchair requiring face to face visit with physician |
| G9157 | Transesoph doppl cardiac mon | Description: Transesophageal doppler measurement of cardiac output (including probe placement, image acquisition, and interpretation per course of treatment) for monitoring purposes |
| G9158 | Motor speech d/c status | Description: Motor speech functional limitation, discharge status, at discharge from therapy or to end reporting |
| G9159 | Lang comp current status | Description: Spoken language comprehension functional limitation, current status at therapy episode outset and at reporting intervals |
| G9160 | Lang comp goal status | Description: Spoken language comprehension functional limitation, projected goal status at therapy episode outset, at reporting intervals, and at discharge or to end reporting |
| G9161 | Lang comp d/c status | Description: Spoken language comprehension functional limitation, discharge status, at discharge from therapy or to end reporting |
| G9162 | Lang express current status | Description: Spoken language expression functional limitation, current status at therapy episode outset and at reporting intervals |
| G9163 | Lang express goal status | Description: Spoken language expression functional limitation, projected goal status at therapy episode outset, at reporting intervals, and at discharge or to end reporting |
| G9164 | Lang express d/c status | Description: Spoken language expression functional limitation, discharge status at discharge from therapy or to end reporting |
| G9165 | Atten current status | Description: Attention functional limitation, current status at therapy episode outset and at reporting intervals |
| G9166 | Atten goal status | Description: Attention functional limitation, projected goal status at therapy episode outset, at reporting intervals, and at discharge or to end reporting |
| G9167 | Atten d/c status | Description: Attention functional limitation, discharge status at discharge from therapy or to end reporting |
| G9168 | Memory current status | Description: Memory functional limitation, current status at therapy episode outset and at reporting intervals |
| G9169 | Memory goal status | Description: Memory functional limitation, projected goal status at therapy episode outset, at reporting intervals, and at discharge or to end reporting |
| G9170 | Memory d/c status | Description: Memory functional limitation, discharge status at discharge from therapy or to end reporting |
| G9171 | Voice current status | Description: Voice functional limitation, current status at therapy episode outset and at reporting intervals |
| G9172 | Voice goal status | Description: Voice functional limitation, projected goal status at therapy episode outset, at reporting intervals, and at discharge or to end reporting |
| G9173 | Voice d/c status | Description: Voice functional limitation, discharge status at discharge from therapy or to end reporting |
| G9174 | Speech lang current status | Description: Other speech language pathology functional limitation, current status at therapy episode outset and at reporting intervals |
| G9175 | Speech lang goal status | Description: Other speech language pathology functional limitation, projected goal status at therapy episode outset, at reporting intervals, and at discharge or to end reporting |
| G9176 | Speech lang d/c status | Description: Other speech language pathology functional limitation, discharge status at discharge from therapy or to end reporting |
| G9186 | Motor speech goal status | Description: Motor speech functional limitation, projected goal status at therapy episode outset, at reporting intervals, and at discharge or to end reporting |
| G9187 | Bpci home visit | Description: Bundled payments for care improvement initiative home visit for patient assessment performed by a qualified health care professional for individuals not considered homebound including, but not limited to, assessment of safety, falls, clinical status, fluid status, medication reconciliation/management, patient compliance with orders/plan of care, performance of activities of daily living, appropriateness of care setting; (for use only in the meidcare-approved bundled payments for care improvement initiative); may not be billed for a 30-day period covered by a transitional care management code |
| G9188 | Beta not given no reason | Description: Beta-blocker therapy not prescribed, reason not given |
| G9189 | Beta pres or already taking | Description: Beta-blocker therapy prescribed or currently being taken |
| G9190 | Medical reason for no beta | Description: Documentation of medical reason(s) for not prescribing beta-blocker therapy (eg, allergy, intolerance, other medical reasons) |
| G9191 | Pt reason for no beta | Description: Documentation of patient reason(s) for not prescribing beta-blocker therapy (eg, patient declined, other patient reasons) |
| G9192 | System reason for no beta | Description: Documentation of system reason(s) for not prescribing beta-blocker therapy (eg, other reasons attributable to the health care system) |
| G9193 | Doc not eligible for dep med | Description: Clinician documented that patient with a diagnosis of major depression was not an eligible candidate for antidepressant medication treatment or patient did not have a diagnosis of major depression |
| G9194 | Mdd pt treated for 180d | Description: Patient with a diagnosis of major depression documented as being treated with antidepressant medication during the entire 180 day (6 month) continuation treatment phase |
| G9195 | Mdd pt not treated for 180d | Description: Patient with a diagnosis of major depression not documented as being treated with antidepressant medication during the entire 180 day (6 months) continuation treatment phase |
| G9196 | Med reason for no ceph | Description: Documentation of medical reason(s) for not ordering a first or second generation cephalosporin for antimicrobial prophylaxis (e.g., patients enrolled in clinical trials, patients with documented infection prior to surgical procedure of interest, patients who were receiving antibiotics more than 24 hours prior to surgery [except colon surgery patients taking oral prophylactic antibiotics], patients who were receiving antibiotics within 24 hours prior to arrival [except colon surgery patients taking oral prophylactic antibiotics], other medical reason(s)) |
| G9197 | Order for ceph | Description: Documentation of order for first or second generation cephalosporin for antimicrobial prophylaxis |
| G9198 | No order for ceph no reason | Description: Order for first or second generation cephalosporin for antimicrobial prophylaxis was not documented, reason not given |
| G9199 | Doc reason for no vte | Description: Venous thromboembolism (vte) prophylaxis not administered the day of or the day after hospital admission for documented reasons (eg, patient is ambulatory, patient expired during inpatient stay, patient already on warfarin or another anticoagulant, other medical reason(s) or eg, patient left against medical advice, other patient reason(s)) |
| G9200 | No reason for no vte | Description: Venous thromboembolism (vte) prophylaxis was not administered the day of or the day after hospital admission, reason not given |
| G9201 | Vte given upon admission | Description: Venous thromboembolism (vte) prophylaxis administered the day of or the day after hospital admission |
| G9202 | Hep c aby pos | Description: Patients with a positive hepatitis c antibody test |
| G9203 | Hep c rna done prior to med | Description: Rna testing for hepatitis c documented as performed within 12 months prior to initiation of antiviral treatment for hepatitis c |
| G9204 | No reason for no hep c rna | Description: Rna testing for hepatitis c was not documented as performed within 12 months prior to initiation of antiviral treatment for hepatitis c, reason not given |
| G9205 | Hep c antiviral started | Description: Patient starting antiviral treatmentfor hepatitis c during the measurement period |
| G9206 | Hep c therapy started | Description: Patient starting antiviral treatment for hepatitis c during the measurement period |
| G9207 | Hep c genotype prior to med | Description: Hepatitis c genotype testing documented as performed within 12 months prior to initiation of antiviral treatment for hepatitis c |
| G9208 | No reason for no hep c geno | Description: Hepatitis c genotype testing was not documented as performed within 12 months prior to initiation of antiviral treatment for hepatitis c, reason not given |
| G9209 | Hep c rna 4to12 wk after med | Description: Hepatitis c quantitative rna testing documented as performed between 4-12 weeks after the initiation of antiviral treatment |
| G9210 | No hepc rna after med docrsn | Description: Hepatitis c quantitative rna testing not performed between 4-12 weeks after the initiation of antiviral treatment for documented reason(s) (e.g., patients whose treatment was discontinued during the testing period prior to testing, other medical reasons, patient declined, other patient reasons) |
| G9211 | No hepc rna after med no rsn | Description: Hepatitis c quantitative rna testing was not documented as performed between 4-12 weeks after the initiation of antiviral treatment, reason not given |
| G9212 | Doc of dsm-iv init eval | Description: Dsm-ivtm criteria for major depressive disorder documented at the initial evaluation |
| G9213 | No doc of dsm-iv | Description: Dsm-iv-tr criteria for major depressive disorder not documented at the initial evaluation, reason not otherwise specified |
| G9214 | Cd4 count documented | Description: Cd4+ cell count or cd4+ cell percentage results documented |
| G9215 | No cd4 count no reason | Description: Cd4+ cell count or percentage not documented as performed, reason not given |
| G9216 | No pcp proph at dx no reason | Description: Pcp prophylaxis was not prescribed at time of diagnosis of hiv, reason not given |
| G9217 | No pcp proph low cd4 norsn | Description: Pcp prophylaxis was not prescribed within 3 months of low cd4+ cell count below 200 cells/mm3, reason not given |
| G9218 | No pcp prop low at cd4 norsn | Description: Pcp prophylaxis was not prescribed within 3 months oflow cd4+ cell count below 500 cells/mm3 or a cd4 percentage below 15%, reason not given |
| G9219 | No oder pjp for med reason | Description: Pneumocystis jiroveci pneumonia prophylaxis not prescribed within 3 months of low cd4+ cell count below 200 cells/mm3 for medical reason (i.e., patient's cd4+ cell count above threshold within 3 months after cd4+ cell count below threshold, indicating that the patient's cd4+ levels are within an acceptable range and the patient does not require pcp prophylaxis) |
| G9220 | No order for pjp for medrsn | Description: Pneumocystis jiroveci pneumonia prophylaxis not prescribed within 3 months of low cd4+ cell count below 500 cells/mm3 or a cd4 percentage below 15% for medical reason (i.e., patient's cd4+ cell count above threshold within 3 months after cd4+ cell count below threshold, indicating that the patient's cd4+ levels are within an acceptable range and the patient does not require pcp prophylaxis) |
| G9221 | Pjp proph prescribed | Description: Pneumocystis jiroveci pneumonia prophlaxis prescribed |
| G9222 | Pjp proph ordered low cd4 | Description: Pneumocystis jiroveci pneumonia prophylaxis prescribed wthin 3 months of low cd4+ cell count below 200 cells/mm3 |
| G9223 | Pjp proph ordered cd4 low | Description: Pneumocystis jiroveci pneumonia prophylaxis prescribed within 3 months of low cd4+ cell count below 500 cells/mm3 or a cd4 percentage below 15% |
| G9224 | Medrsn no foot exam | Description: Documentation of medical reason for not performing foot exam (e.g., patient with bilateral foot/leg amputation) |
| G9225 | Norsn no foot exam | Description: Foot exam was not performed, reason not given |
| G9226 | 3 comp foot exam completed | Description: Foot examination performed (includes examination through visual inspection, sensory exam with 10-g monofilament plus testing any one of the following: vibration using 128-hz tuning fork, pinprick sensation, ankle reflexes, or vibration perception threshold, and pulse exam; report when all of the 3 components are completed) |
| G9227 | Foa doc, care plan not doc | Description: Functional outcome assessment documented, care plan not documented, documentation the patient is not eligible for a care plan at the time of the encounter |
| G9228 | Gc chl syp documented | Description: Chlamydia, gonorrhea and syphilis screening results documented (report when results are present for all of the 3 screenings) |
| G9229 | Ptrsn no gc chl syp test | Description: Chlamydia, gonorrhea, and syphilis screening results not documented (patient refusal is the only allowed exception) |
| G9230 | Norsn for gc chl syp test | Description: Chlamydia, gonorrhea, and syphilis not screened, reason not given |
| G9231 | Doc esrd dia trans preg | Description: Documentation of end stage renal disease (esrd), dialysis, renal transplant before or during the measurement period or pregnancy during the measurement period |
| G9232 | Ptrsn no comm comorbid | Description: Clinician treating major depressive disorder did not communicate to clinician treating comorbid condition for specified patient reason (e.g., patient is unable to communicate the diagnosis of a comorbid condition; the patient is unwilling to communicate the diagnosis of a comorbid condition; or the patient is unaware of the comorbid condition, or any other specified patient reason) |
| G9233 | Tkr composite | Description: All quality actions for the applicable measures in the total knee replacement measures group have been performed for this patient |
| G9234 | Tkr intent | Description: I intend to report the total knee replacement measures group |
| G9235 | Gs mg composite | Description: All quality actions for the applicable measures in the general surgery measures group have been performed for this patient |
| G9236 | Op rad mg composite | Description: All quality actions for the applicable measures in the optimizing patient exposure to ionizing radiation measures group have been performed for this patient |
| G9237 | Gs mg intent | Description: I intend to report the general surgery measures group |
| G9238 | Op rad mg intent | Description: I intend to report the optimizing patient exposure to ionizing radiation measures group |
| G9239 | Doc rsn hemod & cath acc | Description: Documentation of reasons for patient initiating maintenance hemodialysis with a catheter as the mode of vascular access (e.g., patient has a maturing arteriovenous fistula (avf)/arteriovenous graft (avg), time-limited trial of hemodialysis, other medical reasons, patient declined avf/avg, other patient reasons, patient followed by reporting nephrologist for fewer than 90 days, other system reasons) |
| G9240 | Doc pt w cath maint dia | Description: Patient whose mode of vascular access is a catheter at the time maintenance hemodialysis is initiated |
| G9241 | Doc pt w out cath maint dia | Description: Patient whose mode of vascular access is not a catheter at the time maintenance hemodialysis is initiated |
| G9242 | Doc viral load >=200 | Description: Documentation of viral load equal to or greater than 200 copies/ml or viral load not performed |
| G9243 | Doc viral load <200 | Description: Documentation of viral load less than 200 copies/ml |
| G9244 | Antiviral not ordered | Description: Antiretroviral thereapy not prescribed |
| G9245 | Antiviral ordered | Description: Antiretroviral therapy prescribed |
| G9246 | No enc or enc/vir ld 90days | Description: Patient did not have two eligible encounters at least 90 days apart or one eligible encounter and one hiv viral load test at least 90 days apart |
| G9247 | 2 enc enc/vir ld 90d | Description: Patient had two eligible encounters at least 90 days apart or one eligible encounter and one hiv viral load test at least 90 days apart |
| G9248 | No med visit 6mo | Description: Patient did not have a medical visit in the last 6 months |
| G9249 | Med visit w in 6mo | Description: Patient had a medical visit in the last 6 months |
| G9250 | Doc of pain comfort 48hr | Description: Documentation of patient pain brought to a comfortable level within 48 hours from initial assessment |
| G9251 | Doc no pain comfort 48hr | Description: Documentation of patient with pain not brought to a comfortable level within 48 hours from initial assessment |
| G9252 | Neo detect scrn colo | Description: Adenoma(s) or other neoplasm detected during screening colonoscopy |
| G9253 | No neo detect scrn colo | Description: Adenoma(s) or other neoplasm not detected during screening colonoscopy |
| G9254 | Doc pt dischg >2d | Description: Documentation of patient discharged to home later than post-operative day 2 following cea or cas |
| G9255 | Pt dc home 2nd po day | Description: Documentation of patient discharged to home no later than post operative day 2 following cea or cas |
| G9256 | Doc of pat death after cas | Description: Documentation of patient death following cas |
| G9257 | Doc of pat stroke after cas | Description: Documentation of patient stroke following cas |
| G9258 | Doc of pat stroke after cea | Description: Documentation of patient stroke following cea |
| G9259 | Survive/no stroke post cas | Description: Documentation of patient survival and absence of stroke following cas |
| G9260 | Doc of pat death after cea | Description: Documentation of patient death following cea |
| G9261 | Survive/no stroke post cea | Description: Documentation of patient survival and absence of stroke following cea |
| G9262 | Doc of death post-aaa repair | Description: Documentation of patient death in the hospital following endovascular aaa repair |
| G9263 | Doc of disch post-aaa repair | Description: Documentation of patient discharged alive following endovascular aaa repair |
| G9264 | Doc rsn hemod w/cath >=90d | Description: Documentation of patient receiving maintenance hemodialysis for greater than or equal to 90 days with a catheter for documented reasons (e.g., other medical reasons, patient declined arteriovenous fistula (avf)/arteriovenous graft (avg), other patient reasons) |
| G9265 | Doc cath >90d for maint dia | Description: Patient receiving maintenance hemodialysis for greater than or equal to 90 days with a catheter as the mode of vascular access |
| G9266 | Norsn pt cath >=90d | Description: Patient receiving maintenance hemodialysis for greater than or equal to 90 days without a catheter as the mode of vascular access |
| G9267 | Doc comp or mort w in 30d | Description: Documentation of patient with one or more complications or mortality within 30 days |
| G9268 | Doc comp or mort w in 90d | Description: Documentation of patient with one or more complications within 90 days |
| G9269 | Doc no comp or mort w in 30d | Description: Documentation of patient without one or more complications and without mortality within 30 days |
| G9270 | Doc no comp or mort w in 90d | Description: Documentation of patient without one or more complications within 90 days |
| G9271 | Ldl under 100 | Description: Ldl value < 100 |
| G9272 | Ldl 100 and over | Description: Ldl value >= 100 |
| G9273 | Sys<140 and dia<90 | Description: Blood pressure has a systolic value of < 140 and a diastolic value of < 90 |
| G9274 | Bp out of nrml limits | Description: Blood pressure has a systolic value of =140 and a diastolic value of = 90 or systolic value < 140 and diastolic value = 90 or systolic value = 140 and diastolic value < 90 |
| G9275 | Doc of non tobacco user | Description: Documentation that patient is a current non-tobacco user |
| G9276 | Doc of tobacco user | Description: Documentation that patient is a current tobacco user |
| G9277 | Doc daily aspirin or contra | Description: Documentation that the patient is on daily aspirin or anti-platelet or has documentation of a valid contraindication or exception to aspirin/anti-platelet; contraindications/exceptions include anti-coagulant use, allergy to aspirin or anti-platelets, history of gastrointestinal bleed and bleeding disorder; additionally, the following exceptions documented by the physician as a reason for not taking daily aspirin or anti-platelet are acceptable (use of non-steroidal anti-inflammatory agents, documented risk for drug interaction, uncontrolled hypertension defined as >180 systolic or >110 diastolic or gastroesophageal reflux) |
| G9278 | Doc no daily aspirin | Description: Documentation that the patient is not on daily aspirin or anti-platelet regimen |
| G9279 | Pne scrn done doc vac done | Description: Pneumococcal screening performed and documentation of vaccination received prior to discharge |
| G9280 | Pne not given norsn | Description: Pneumococcal vaccination not administered prior to discharge, reason not specified |
| G9281 | Pne scrn done doc not ind | Description: Screening performed and documentation that vaccination not indicated/patient refusal |
| G9282 | Doc medrsn no histo type | Description: Documentation of medical reason(s) for not reporting the histological type or nsclc-nos classification with an explanation (e.g., biopsy taken for other purposes in a patient with a history of non-small cell lung cancer or other documented medical reasons) |
| G9283 | Hist type doc on report | Description: Non small cell lung cancer biopsy and cytology specimen report documents classification into specific histologic type or classified as nsclc-nos with an explanation |
| G9284 | No hist type doc on report | Description: Non small cell lung cancer biopsy and cytology specimen report does not document classification into specific histologic type or classified as nsclc-nos with an explanation |
| G9285 | Site not small cell lung ca | Description: Specimen site other than anatomic location of lung or is not classified as non small cell lung cancer |
| G9286 | Antibio rx w in 10d of sympt | Description: Antibiotic regimen prescribed within 10 days after onset of symptoms |
| G9287 | No antibio w in 10d of sympt | Description: Antibiotic regimen not prescribed within 10 days after onset of symptoms |
| G9288 | Doc medrsn no hist type rpt | Description: Documentation of medical reason(s) for not reporting the histological type or nsclc-nos classification with an explanation (e.g., a solitary fibrous tumor in a person with a history of non-small cell carcinoma or other documented medical reasons) |
| G9289 | Doc type nsm lung ca | Description: Non small cell lung cancer biopsy and cytology specimen report documents classification into specific histologic type or classified as nsclc-nos with an explanation |
| G9290 | No doc type nsm lung ca | Description: Non small cell lung cancer biopsy and cytology specimen report does not document classification into specific histologic type or classified as nsclc-nos with an explanation |
| G9291 | Not nsm lung ca | Description: Specimen site other than anatomic location of lung, is not classified as non small cell lung cancer or classified as nsclc-nos |
| G9292 | Medrsn no pt category | Description: Documentation of medical reason(s) for not reporting pt category and a statement on thickness and ulceration and for pt1, mitotic rate (e.g., negative skin biopsies in a patient with a history of melanoma or other documented medical reasons) |
| G9293 | No pt category on report | Description: Pathology report does not include the pt category and a statement on thickness and ulceration and for pt1, mitotic rate |
| G9294 | Pt cat and thck on report | Description: Pathology report includes the pt category and a statement on thickness and ulceration and for pt1, mitotic rate |
| G9295 | Non cutaneous loc | Description: Specimen site other than anatomic cutaneous location |
| G9296 | Doc share dec prior proc | Description: Patients with documented shared decision-making including discussion of conservative (non-surgical) therapy (e.g., nsaids, analgesics, weight loss, exercise, injections) prior to the procedure |
| G9297 | No doc share dec prior proc | Description: Shared decision-making including discussion of conservative (non-surgical) therapy (e.g., nsaids, analgesics, weight loss, exercise, injections) prior to the procedure, not documented, reason not given |
| G9298 | Eval risk vte card 30d prior | Description: Patients who are evaluated for venous thromboembolic and cardiovascular risk factors within 30 days prior to the procedure (e.g., history of dvt, pe, mi, arrhythmia and stroke) |
| G9299 | No eval risk vte card prior | Description: Patients who are not evaluated for venous thromboembolic and cardiovascular risk factors within 30 days prior to the procedure (e.g., history of dvt, pe, mi, arrhythmia and stroke, reason not given) |
| G9300 | Doc medrsn no compl antibio | Description: Documentation of medical reason(s) for not completely infusing the prophylactic antibiotic prior to the inflation of the proximal tourniquet (e.g., a tourniquet was not used) |
| G9301 | Doc compl inf antibio | Description: Patients who had the prophylactic antibiotic completely infused prior to the inflation of the proximal tourniquet |
| G9302 | Norsn incomp inf antibio | Description: Prophylactic antibiotic not completely infused prior to the inflation of the proximal tourniquet, reason not given |
| G9303 | Norsn no pros info op rpt | Description: Operative report does not identify the prosthetic implant specifications including the prosthetic implant manufacturer, the brand name of the prosthetic implant and the size of each prosthetic implant, reason not given |
| G9304 | Pros info op rpt | Description: Operative report identifies the prosthetic implant specifications including the prosthetic implant manufacturer, the brand name of the prosthetic implant and the size of each prosthetic implant |
| G9305 | No interv req for leak | Description: Intervention for presence of leak of endoluminal contents through an anastomosis not required |
| G9306 | Interv req for leak | Description: Intervention for presence of leak of endoluminal contents through an anastomosis required |
| G9307 | No ret for surg w in 30d | Description: No return to the operating room for a surgical procedure, for complications of the principal operative procedure, within 30 days of the principal operative procedure |
| G9308 | Unpl ret or w/compl w/in 30d | Description: Unplanned return to the operating room for a surgical procedure, for complications of the principal operative procedure, within 30 days of the principal operative procedure |
| G9309 | No unplnd hosp readm in 30d | Description: No unplanned hospital readmission within 30 days of principal procedure |
| G9310 | Unplnd hosp readm in 30d | Description: Unplanned hospital readmission within 30 days of principal procedure |
| G9311 | No surg site infection | Description: No surgical site infection |
| G9312 | Surgical site infection | Description: Surgical site infection |
| G9313 | Amoxic not presc as 1st line | Description: Amoxicillin, with or without clavulanate, not prescribed as first line antibiotic at the time of diagnosis for documented reason |
| G9314 | Norsn not first line amox | Description: Amoxicillin, with or without clavulanate, not prescribed as first line antibiotic at the time of diagnosis, reason not given |
| G9315 | Amox w/wo clav rx | Description: Amoxicillin, with or without clavulanate, prescribed as a first line antibiotic at the time of diagnosis |
| G9316 | Doc comm risk calc | Description: Documentation of patient-specific risk assessment with a risk calculator based on multi-institutional clinical data, the specific risk calculator used, and communication of risk assessment from risk calculator with the patient or family |
| G9317 | No doc comm risk calc | Description: Documentation of patient-specific risk assessment with a risk calculator based on multi-institutional clinical data, the specific risk calculator used, and communication of risk assessment from risk calculator with the patient or family not completed |
| G9318 | Image std nomenclature | Description: Imaging study named according to standardized nomenclature |
| G9319 | Image not std nomenclature | Description: Imaging study not named according to standardized nomenclature, reason not given |
| G9320 | Medrsn no std nomenclature | Description: Documentation of medical reason(s) for not naming ct studies according to a standardized nomenclature provided (eg, ct studies performed for radiation treatment planning or image-guided radiation treatment delivery) |
| G9321 | Prev ct nuc med cnt doc 12mo | Description: Count of previous ct (any type of ct) and cardiac nuclear medicine (myocardial perfusion or infarct avid imaging) studies documented in the 12-month period prior to the current study |
| G9322 | No cnt ct nuc med doc 12mo | Description: Count of previous ct and cardiac nuclear medicine (myocardial perfusion or infarct avid imaging) studies not documented in the 12-month period prior to the current study, reason not given |
| G9323 | Mdrsn no doc cnt of ct | Description: Documentation of medical reason(s) for not counting previous ct and cardiac nuclear medicine (myocardial perfusion) studies (eg, ct studies performed for radiation treatment planning or image-guided radiation treatment delivery) |
| G9324 | Not all data norsn | Description: All necessary data elements not included, reason not given |
| G9325 | Medrsn no ct rpt to reg | Description: Ct studies not reported to a radiation dose index registry due to medical reasons (eg, ct studies performed for radiation treatment planning or image-guided radiation treatment delivery) |
| G9326 | Ct done no rad ds index, nrg | Description: Ct studies performed not reported to a radiation dose index registry that is capable of collecting at a minimum all necessary data elements, reason not given |
| G9327 | Ct done rad ds index | Description: Ct studies performed reported to a radiation dose index registry that is capable of collecting at a minimum all necessary data elements |
| G9328 | Medrsn no dicom format doc | Description: Dicom format image data availability not documented in final report due to medical reasons (eg, ct studies performed for radiation treatment planning or image-guided radiation treatment delivery) |
| G9329 | Norsn no dicom format doc | Description: Dicom format image data available to non-affiliated external healthcare facilities or entities on a secure, media free, reciprocally searchable basis with patient authorization for at least a 12-month period after the study not documented in final report, reason not given |
| G9340 | Dicom format doc on rpt | Description: Final report documented that dicom format image data available to non-affiliated external healthcare facilities or entities on a secure, media free, reciprocally searchable basis with patient authorization for at least a 12-month period after the study |
| G9341 | Srch for ct w in 12 mos | Description: Search conducted for prior patient ct studies completed at non-affiliated external healthcare facilities or entities within the past 12-months and are available through a secure, authorized, media-free, shared archive prior to an imaging study being performed |
| G9342 | No srch for ct in 12mo norsn | Description: Search not conducted prior to an imaging study being performed for prior patient ct studies completed at non-affiliated external healthcare facilities or entities within the past 12-months and are available through a secure, authorized, media-free, shared archive, reason not given |
| G9343 | Medrsn no dicom srch | Description: Due to medical reasons, search not conducted for dicom format images for prior patient ct imaging studies completed at non-affiliated external healthcare facilities or entities within the past 12 months that are available through a secure, authorized, media-free, shared archive (e.g., ct studies performed for radiation treatment planning or image-guided radiation treatment delivery) |
| G9344 | Sysrsn no dicom srch | Description: Due to system reasons search not conducted for dicom format images for prior patient ct imaging studies completed at non-affiliated external healthcare facilities or entities within the past 12 months that are available through a secure, authorized, media-free, shared archive (e.g., non-affiliated external healthcare facilities or entities does not have archival abilities through a shared archival system) |
| G9345 | Follow up pulm nod | Description: Follow-up recommendations documented according to recommended guidelines for incidentally detected pulmonary nodules (e.g., follow-up ct imaging studies needed or that no follow-up is needed) based at a minimum on nodule size and patient risk factors |
| G9346 | No follow up pulm nod | Description: Follow-up recommendations not documented according to recommended guidelines for incidentally detected pulmonary nodules due to medical reasons (e.g., patients with known malignant disease, patients with unexplained fever, ct studies performed for radiation treatment planning or image-guided radiation treatment delivery) |
| G9347 | No follow up pulm nod norsn | Description: Follow-up recommendations not documented according to recommended guidelines for incidentally detected pulmonary nodules, reason not given |
| G9348 | Doc rsn for ord ct scan | Description: Ct scan of the paranasal sinuses ordered at the time of diagnosis for documented reasons |
| G9349 | Ct within 28 days | Description: Ct scan of the paranasal sinuses ordered at the time of diagnosis or received within 28 days after date of diagnosis |
| G9350 | No doc sinus ct 28d or dx | Description: Ct scan of the paranasal sinuses not ordered at the time of diagnosis or received within 28 days after date of diagnosis |
| G9351 | Doc >1 sinus ct w 90d dx | Description: More than one ct scan of the paranasal sinuses ordered or received within 90 days after diagnosis |
| G9352 | Not >1 sinus ct w 90d dx | Description: More than one ct scan of the paranasal sinuses ordered or received within 90 days after the date of diagnosis, reason not given |
| G9353 | Medrsn >1 sinus ct w 90d dx | Description: More than one ct scan of the paranasal sinuses ordered or received within 90 days after the date of diagnosis for documented reasons (eg, patients with complications, second ct obtained prior to surgery, other medical reasons) |
| G9354 | 1 or no ct sinus w/in 90d dx | Description: One ct scan or no ct scan of the paranasal sinuses ordered within 90 days after the date of diagnosis |
| G9355 | No early ind/delivery | Description: Elective delivery (without medical indication) by cesarean birth or induction of labor not performed (<39 weeks of gestation) |
| G9356 | Early ind/delivery | Description: Elective delivery (without medical indication) by cesarean birth or induction of labor performed (<39 weeks of gestation) |
| G9357 | Pp eval/edu perf | Description: Post-partum screenings, evaluations and education performed |
