LD TECHNOLOGY

CPT CODES

SUGGESTED

CPT CODES

cpt codes Chronic Care Management - LD Technology

When billing the suggested CPT Codes, we recommend that you identify the appropriate FDA 510k medical device technology that corresponds to each suggested CPT Code. We don’t recommend identifying the TM FLOW System when billing because it is merely a platform that contains each of our various FDA 510K medical technologies:- Sweat C, OXI W, TBL-ABI.                               

 LD technology products / medical devices are NOT automated devices. Our products require trained technician involvement, and our reports require qualified physician interpretation. 

CPT CODING 95921 FROM CMS

CPT CODING 95921 FROM CMS

Testing of autonomic nervous system function; Cardiovagal innervation(parasympathetic function), including 2 or more of the following: Heart rate response to deep breathing with recorded R-R intervals, Valsalva Ratio, and 30:15 Ratio. 
We recommend that you identify the “OXI_W Device ” and not TM Flow when billing this CPT Code. 

CPT CODING 95923 FROM CMS

CPT CODING 95923 FROM CMS

Sudomotor-function testing is used to evaluate and document neuropathic disturbances that may be associated with pain. The quantitative sudomotor axon reflex test (QSART), thermoregulatory sweat test (TST), sympathetic skin responses, and silastic sweat imprints are tests of sympathetic cholinergic sudomotor function.                                                                                                           We recommend that you identify the “SWEAT C” and not TM Flow when billing this CPT Code

*Method: Changes in sympathetic skin potential.Sympathetic peripheral autonomic skin (or surface) potentials (PASPs).

SWEATC AND ARTICLE A54954 OF NOVITAS

SWEATC AND ARTICLE A54954 OF NOVITAS

Sweat C is not an ESC device. The word ESC means Electrochemical Skin response.
The article A54954 states: “The device measuring ESC “consist of two sets of large-area stainless steel electrodes for the hands and feet that are connected to a computer for recording and data-management purposes. The electrodes are alternately used as an anode or cathode, and a direct current incremental voltage of ≤4 V is applied to the anode. Through reverse iontophoresis, the device generates voltage to the cathode and a current (intensity of around 0.2 mA) between the anode and cathode proportional to chloride concentration.”

SweatC shall NOT be considered in this category for the following reasons:

SweatC shall NOT be considered in this category for the following reasons:

1. It does not use steel electrodes for the hand and feet
2. It does not use incremental voltage. but constant voltage
3. It uses cloth electrodes (textile fibers) so no electrochemical reaction can be obtained, and therefore it cannot induce any reverse iontophoresis.

CPT CODING 93922 FROM CMS

CPT CODING 93922 FROM CMS

Limited bilateral noninvasive physiologic studies of upper or lower extremity arteries, (eg, for lower extremity: ankle/brachial indices at distal posterior tibial and anterior tibial/dorsalis pedis arteries plus bidirectional, doppler waveform recording and analysis at 1-2 levels, or ankle/brachial indices at distal posterior tibial and anterior tibial/dorsalis pedis arteries plus volume plethysmography at 1-2 levels, or ankle/brachial indices at distal posterior tibial and anterior tibial/dorsalis pedis arteries with, transcutaneous oxygen tension measurement at 1-2 levels).                                                                                                                        We recommend that you identify the “TBL-ABI device” and not TM Flow when billing this CPT Code.                   

TBL-ABI device measures ankle/brachial indices at distal posterior tibial and anterior tibial/dorsalis pedis arteries plus volume plethysmography at 2 levels.


*DISCLAIMERS: The above check list of CPT Codes are only suggested according to the  cleared intended use of each LD Technology product, and it cannot be considered as a part of the device performances. The practitioner is solely responsible for compliance in the use of CPT codes and related ICD-10’s according to the guidelines established by the AMA (American Medical Association) and CMS (Center for Medicare and Medicaid Services) Central Office per state or region.  LD TECHNOLOGY shall not be liable for any changes from the AMA and/or CMS and/or for any financial damage resulting from the suggested CPT  in case of practitioner’s Audit.

*It is the Physicians sole responsiblity to ensure that they have the knowledge, training, expertise, and accreditation to perform these tests.  The accreditation requirements are provided by CMS.BL

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