HCPCS Level II › G

HCPCS Level II codes starting with G

2,011 codes, page 14 of 21. Every code ever valid for billing is listed, including those now retired.

CodeDescriptionStatus
G9221 Pneumocystis jiroveci pneumonia prophlaxis prescribed through FY2026 Terminated
G9222 Pneumocystis jiroveci pneumonia prophylaxis prescribed wthin 3 months of low cd4+ cell count below 200 cells/mm3 through FY2026 Terminated
G9223 Pneumocystis jiroveci pneumonia prophylaxis prescribed within 3 months of low cd4+ cell count below 500 cells/mm3 or a cd4 percentage below 15% Valid
G9224 Documentation of medical reason for not performing foot exam (e.g., patient with bilateral foot/leg amputation) through FY2026 Terminated
G9225 Foot exam was not performed, reason not given Valid
G9226 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) Valid
G9227 Functional outcome assessment documented, care plan not documented, documentation the patient is not eligible for a care plan at the time of the encounter Valid
G9228 Chlamydia, gonorrhea and syphilis screening results documented (report when results are present for all of the 3 screenings) Valid
G9229 Chlamydia, gonorrhea, and syphilis screening results not documented (patient refusal is the only allowed exception) through FY2026 Terminated
G9230 Chlamydia, gonorrhea, and syphilis not screened, reason not given Valid
G9231 Documentation of end stage renal disease (esrd), dialysis, renal transplant before or during the measurement period or pregnancy during the measurement period Valid
G9232 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) through FY2026 Terminated
G9233 All quality actions for the applicable measures in the total knee replacement measures group have been performed for this patient through FY2026 Terminated
G9234 I intend to report the total knee replacement measures group through FY2026 Terminated
G9235 All quality actions for the applicable measures in the general surgery measures group have been performed for this patient through FY2026 Terminated
G9236 All quality actions for the applicable measures in the optimizing patient exposure to ionizing radiation measures group have been performed for this patient through FY2026 Terminated
G9237 I intend to report the general surgery measures group through FY2026 Terminated
G9238 I intend to report the optimizing patient exposure to ionizing radiation measures group through FY2026 Terminated
G9239 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) through FY2026 Terminated
G9240 Patient whose mode of vascular access is a catheter at the time maintenance hemodialysis is initiated through FY2026 Terminated
G9241 Patient whose mode of vascular access is not a catheter at the time maintenance hemodialysis is initiated through FY2026 Terminated
G9242 Documentation of viral load equal to or greater than 200 copies/ml or viral load not performed Valid
G9243 Documentation of viral load less than 200 copies/ml Valid
G9244 Antiretroviral thereapy not prescribed through FY2026 Terminated
G9245 Antiretroviral therapy prescribed through FY2026 Terminated
G9246 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 Valid
G9247 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 Valid
G9248 Patient did not have a medical visit in the last 6 months through FY2026 Terminated
G9249 Patient had a medical visit in the last 6 months through FY2026 Terminated
G9250 Documentation of patient pain brought to a comfortable level within 48 hours from initial assessment through FY2026 Terminated
G9251 Documentation of patient with pain not brought to a comfortable level within 48 hours from initial assessment through FY2026 Terminated
G9252 Adenoma(s) or other neoplasm detected during screening colonoscopy through FY2026 Terminated
G9253 Adenoma(s) or other neoplasm not detected during screening colonoscopy through FY2026 Terminated
G9254 Documentation of patient discharged to home later than post-operative day 2 following cea or cas Valid
G9255 Documentation of patient discharged to home no later than post operative day 2 following cea or cas Valid
G9256 Documentation of patient death following cas through FY2026 Terminated
G9257 Documentation of patient stroke following cas through FY2026 Terminated
G9258 Documentation of patient stroke following cea through FY2026 Terminated
G9259 Documentation of patient survival and absence of stroke following cas through FY2026 Terminated
G9260 Documentation of patient death following cea through FY2026 Terminated
G9261 Documentation of patient survival and absence of stroke following cea through FY2026 Terminated
G9262 Documentation of patient death in the hospital following endovascular aaa repair through FY2026 Terminated
G9263 Documentation of patient discharged alive following endovascular aaa repair through FY2026 Terminated
G9264 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) through FY2026 Terminated
G9265 Patient receiving maintenance hemodialysis for greater than or equal to 90 days with a catheter as the mode of vascular access through FY2026 Terminated
G9266 Patient receiving maintenance hemodialysis for greater than or equal to 90 days without a catheter as the mode of vascular access through FY2026 Terminated
G9267 Documentation of patient with one or more complications or mortality within 30 days through FY2026 Terminated
G9268 Documentation of patient with one or more complications within 90 days through FY2026 Terminated
G9269 Documentation of patient without one or more complications and without mortality within 30 days through FY2026 Terminated
G9270 Documentation of patient without one or more complications within 90 days through FY2026 Terminated
G9271 Ldl value < 100 through FY2026 Terminated
G9272 Ldl value >= 100 through FY2026 Terminated
G9273 Blood pressure has a systolic value of < 140 and a diastolic value of < 90 Valid
G9274 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 Valid
G9275 Documentation that patient is a current non-tobacco user Valid
G9276 Documentation that patient is a current tobacco user Valid
G9277 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) Valid
G9278 Documentation that the patient is not on daily aspirin or anti-platelet regimen Valid
G9279 Pneumococcal screening performed and documentation of vaccination received prior to discharge Valid
G9280 Pneumococcal vaccination not administered prior to discharge, reason not specified Valid
G9281 Screening performed and documentation that vaccination not indicated/patient refusal Valid
G9282 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) Valid
G9283 Non small cell lung cancer biopsy and cytology specimen report documents classification into specific histologic type or classified as nsclc-nos with an explanation Valid
G9284 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 Valid
G9285 Specimen site other than anatomic location of lung or is not classified as non small cell lung cancer Valid
G9286 Antibiotic regimen prescribed within 10 days after onset of symptoms Valid
G9287 Antibiotic regimen not prescribed within 10 days after onset of symptoms Valid
G9288 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) Valid
G9289 Non small cell lung cancer biopsy and cytology specimen report documents classification into specific histologic type or classified as nsclc-nos with an explanation Valid
G9290 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 Valid
G9291 Specimen site other than anatomic location of lung, is not classified as non small cell lung cancer or classified as nsclc-nos Valid
G9292 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) Valid
G9293 Pathology report does not include the pt category and a statement on thickness and ulceration and for pt1, mitotic rate Valid
G9294 Pathology report includes the pt category and a statement on thickness and ulceration and for pt1, mitotic rate Valid
G9295 Specimen site other than anatomic cutaneous location Valid
G9296 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 Valid
G9297 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 Valid
G9298 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) Valid
G9299 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) Valid
G9300 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) through FY2026 Terminated
G9301 Patients who had the prophylactic antibiotic completely infused prior to the inflation of the proximal tourniquet through FY2026 Terminated
G9302 Prophylactic antibiotic not completely infused prior to the inflation of the proximal tourniquet, reason not given through FY2026 Terminated
G9303 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 through FY2026 Terminated
G9304 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 through FY2026 Terminated
G9305 Intervention for presence of leak of endoluminal contents through an anastomosis not required Valid
G9306 Intervention for presence of leak of endoluminal contents through an anastomosis required Valid
G9307 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 Valid
G9308 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 Valid
G9309 No unplanned hospital readmission within 30 days of principal procedure Valid
G9310 Unplanned hospital readmission within 30 days of principal procedure Valid
G9311 No surgical site infection Valid
G9312 Surgical site infection Valid
G9313 Amoxicillin, with or without clavulanate, not prescribed as first line antibiotic at the time of diagnosis for documented reason Valid
G9314 Amoxicillin, with or without clavulanate, not prescribed as first line antibiotic at the time of diagnosis, reason not given Valid
G9315 Amoxicillin, with or without clavulanate, prescribed as a first line antibiotic at the time of diagnosis Valid
G9316 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 Valid
G9317 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 Valid
G9318 Imaging study named according to standardized nomenclature Valid
G9319 Imaging study not named according to standardized nomenclature, reason not given Valid
G9320 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) through FY2026 Terminated
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