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Official Description

Ambulatory blood pressure monitoring, utilizing report-generating software, automated, worn continuously for 24 hours or longer; recording only

© Copyright 2025 American Medical Association. All rights reserved.

Common Language Description

Ambulatory blood pressure monitoring is a diagnostic procedure designed to assess blood pressure variations over an extended period, typically 24 hours or longer. This method is particularly useful for capturing blood pressure readings during a patient's normal daily activities, which can provide insights into their blood pressure behavior outside of a clinical environment. The procedure involves the use of a portable blood pressure monitoring device that is worn continuously, allowing for the collection of data at regular intervals. This continuous monitoring can help identify conditions such as white coat hypertension, where a patient's blood pressure may be elevated in a clinical setting due to anxiety, as well as nocturnal hypertension, which refers to elevated blood pressure during sleep. Additionally, it can evaluate the effectiveness of antihypertensive medications by monitoring how well they control blood pressure throughout the day and night. The device consists of a blood pressure cuff that is placed around the upper arm and a compact digital monitor that can be secured to a belt. The monitor is programmed to automatically inflate the cuff, measure the blood pressure, and record the readings at specified intervals. After the monitoring period, the device is returned to the healthcare provider, who utilizes report-generating software to analyze the collected data. It is important to note that specific CPT® codes are designated for different aspects of this procedure: code 93784 is used when recording, scanning analysis, and interpretation with a report are performed; code 93786 is for recording only; code 93788 is for scanning analysis and report only; and code 93790 is for a review of the procedure with interpretation and report.

© Copyright 2025 Coding Ahead. All rights reserved.

1. Indications

Ambulatory blood pressure monitoring is indicated for several clinical scenarios, including:

  • Assessment of Blood Pressure Variability This procedure is performed to identify fluctuations in blood pressure over a 24-hour period, which can provide valuable information about a patient's overall cardiovascular health.
  • Evaluation of White Coat Hypertension It helps determine if a patient experiences elevated blood pressure readings in a clinical setting due to anxiety, which may not reflect their true blood pressure levels during daily activities.
  • Monitoring Nocturnal Hypertension The procedure can assess whether a patient's blood pressure remains elevated during nighttime hours, which is crucial for understanding their risk for cardiovascular events.
  • Effectiveness of Antihypertensive Medications It is utilized to evaluate how well prescribed blood pressure medications are controlling a patient's blood pressure throughout the day and night.

2. Procedure

The ambulatory blood pressure monitoring procedure involves several key steps:

  • Device Setup The healthcare provider prepares the monitoring device, which includes a blood pressure cuff and a digital recording unit. The cuff is fitted around the patient's upper arm, ensuring a snug but comfortable fit to obtain accurate readings.
  • Programming the Device The device is programmed to take blood pressure measurements at predetermined intervals, typically every 15 to 30 minutes during the day and less frequently at night, depending on the specific protocol established by the healthcare provider.
  • Patient Instructions The patient is instructed on how to wear the device and is advised to continue their normal daily activities while avoiding any strenuous exercise or activities that may interfere with the readings.
  • Continuous Monitoring As the patient goes about their daily routine, the device automatically inflates the cuff, measures the blood pressure, and records the data at the set intervals. This process continues for the entire duration of the monitoring period, which is typically 24 hours or longer.
  • Device Return and Data Analysis After the monitoring period is complete, the patient returns the device to the healthcare provider. The recorded data is then downloaded and analyzed using report-generating software, which compiles the blood pressure readings into a comprehensive report.

3. Post-Procedure

After the ambulatory blood pressure monitoring procedure, the healthcare provider reviews the generated report to assess the patient's blood pressure patterns. The provider may discuss the findings with the patient, including any identified issues such as elevated nighttime blood pressure or significant fluctuations throughout the day. Based on the results, the provider may recommend adjustments to the patient's treatment plan, including medication changes or lifestyle modifications. Follow-up appointments may be scheduled to monitor the patient's progress and ensure effective management of their blood pressure.

Short Descr AMBL BP MNTR W/SW REC ONLY
Medium Descr AMBULATORY BP MNTR W/SW 24 HR+ RECORDING ONLY
Long Descr Ambulatory blood pressure monitoring, utilizing report-generating software, automated, worn continuously for 24 hours or longer; recording only
Status Code Active Code
Global Days XXX - Global Concept Does Not Apply
PC/TC Indicator (26, TC) 3 - Technical Component Only Code
Multiple Procedures (51) 6 - Special payment adjustment rules on the technical component (TC) of multiple diagnostic cardiovascular services apply...
Bilateral Surgery (50) 0 - 150% payment adjustment for bilateral procedures does NOT apply.
Physician Supervisions 01 - Procedure must be performed under the general supervision of a physician.
Assistant Surgeon (80, 82) 0 - Payment restriction for assistants at surgery applies to this procedure...
Co-Surgeons (62) 0 - Co-surgeons not permitted for this procedure.
Team Surgery (66) 0 - Team surgeons not permitted for this procedure.
Diagnostic Imaging Family 99 - Concept Does Not Apply
APC Status Indicator STV-Packaged Codes
Type of Service (TOS) 5 - Diagnostic Laboratory
Berenson-Eggers TOS (BETOS) T2D - Other tests - other
MUE 1
CCS Clinical Classification 62 - Other diagnostic cardiovascular procedures
51 Multiple procedures: when multiple procedures, other than e/m services, physical medicine and rehabilitation services or provision of supplies (eg, vaccines), are performed at the same session by the same individual, the primary procedure or service may be reported as listed. the additional procedure(s) or service(s) may be identified by appending modifier 51 to the additional procedure or service code(s). note: this modifier should not be appended to designated "add-on" codes (see appendix d).
59 Distinct procedural service: under certain circumstances, it may be necessary to indicate that a procedure or service was distinct or independent from other non-e/m services performed on the same day. modifier 59 is used to identify procedures/services, other than e/m services, that are not normally reported together, but are appropriate under the circumstances. documentation must support a different session, different procedure or surgery, different site or organ system, separate incision/excision, separate lesion, or separate injury (or area of injury in extensive injuries) not ordinarily encountered or performed on the same day by the same individual. however, when another already established modifier is appropriate it should be used rather than modifier 59. only if no more descriptive modifier is available, and the use of modifier 59 best explains the circumstances, should modifier 59 be used. note: modifier 59 should not be appended to an e/m service. to report a separate and distinct e/m service with a non-e/m service performed on the same date, see modifier 25.
GA Waiver of liability statement issued as required by payer policy, individual case
XU Unusual non-overlapping service, the use of a service that is distinct because it does not overlap usual components of the main service
Date
Action
Notes
2020-01-01 Changed Code description changed.
2013-01-01 Changed Medium Descriptor changed.
Pre-1990 Added Code added.
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