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M1338 | Similar
HCPCS Codes Similar to M1338
HCPCS Codes Similar to “M1338” Code.
Patients who had follow-up assessment 30 to 180 days after the index assessment who did not demonstrate positive improvement or maintenance of functioning scores during the performance period
M1339
Patients who had follow-up assessment 30 to 180 days after the index assessment who demonstrated positive improvement or maintenance of functioning scores during the performance period
Code added date
: 20240101
Code effective date
: 20240101
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G8653
Risk-adjusted functional status change residual scores for the hip impairment not measured because the patient did not complete the fs status survey near discharge, patient not appropriate
Code added date
: 20110101
Code effective date
: 20200101
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G0248
Demonstration, prior to initiation of home inr monitoring, for patient with either mechanical heart valve(s), chronic atrial fibrillation, or venous thromboembolism who meets medicare coverage criteria, under the direction of a physician; includes: face-to-face demonstration of use and care of the inr monitor, obtaining at least one blood sample, provision of instructions for reporting home inr test results, and documentation of patient's ability to perform testing and report results
Code added date
: 20020701
Code effective date
: 20080319
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G8925
Spirometry test results demonstrate fev1 >= 60% fev1/fvc >= 70%, predicted or patient does not have copd symptoms
Code added date
: 20130101
Code effective date
: 20220101
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M1341
Patients who did not have a follow-up assessment or did not have an assessment within 30 to 180 days after the index assessment during the performance period
Code added date
: 20240101
Code effective date
: 20240101
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M1056
Prescribed anticoagulant medication during the performance period, history of gi bleeding, history of intracranial bleeding, bleeding disorder and specific provider documented reasons: allergy to aspirin or anti-platelets, use of non-steroidal anti-inflammatory agents, drug-drug interaction, uncontrolled hypertension > 180/110 mmhg or gastroesophageal reflux disease
Code added date
: 20190101
Code effective date
: 20190101
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M1036
Adults who have not had at least 180 days of continuous pharmacotherapy with a medication prescribed for oud without a gap of more than seven days
Code added date
: 20190101
Code effective date
: 20190101
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M1465
Patient follow up more than 180 days after treatment
Code added date
: 20260101
Code effective date
: 20260101
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M1463
Documentation of at least two attempts to follow up with patient within 180 days of treatment
Code added date
: 20260101
Code effective date
: 20260101
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M1464
No documentation of at least two attempts to follow up with patient within 180 days of treatment
Code added date
: 20260101
Code effective date
: 20260101
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G2142
Functional status measured by the oswestry disability index (odi version 2.1a) at one year (9 to 15 months) postoperatively was less than or equal to 22 or functional status measured by the odi version 2.1a within three months preoperatively and at one year (9 to 15 months) postoperatively demonstrated an improvement of 30 points or greater
Code added date
: 20200101
Code effective date
: 20220101
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G2143
Functional status measured by the oswestry disability index (odi version 2.1a) at one year (9 to 15 months) postoperatively was greater than 22 and functional status measured by the odi version 2.1a within three months preoperatively and at one year (9 to 15 months) postoperatively demonstrated an improvement of less than 30 points
Code added date
: 20200101
Code effective date
: 20220101
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G2144
Functional status measured by the oswestry disability index (odi version 2.1a) at three months (6-20 weeks) postoperatively was less than or equal to 22 or functional status measured by the odi version 2.1a within three months preoperatively and at three months (6-20 weeks) postoperatively demonstrated an improvement of 30 points or greater
Code added date
: 20200101
Code effective date
: 20220101
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G2145
Functional status measured by the oswestry disability index (odi version 2.1a) at three months (6 - 20 weeks) postoperatively was greater than 22 and functional status measured by the odi version 2.1a within three months preoperatively and at three months (6 - 20 weeks) postoperatively demonstrated an improvement of less than 30 points
Code added date
: 20200101
Code effective date
: 20220101
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