![]() | Clinical UM Guideline |
Subject: Back-Up Ventilators in the Home Setting | |
Guideline #: CG-DME-26 | Publish Date: 10/01/2024 |
Status: Reviewed | Last Review Date: 08/08/2024 |
Description |
This document addresses the medically necessary indications for the use of back-up (or second additional) ventilators in the home setting, for use as a “back-up” machine, if needed.
Mechanical ventilation may be defined as a life support system designed to replace or support normal ventilatory lung function (AARC 2007).
Clinical Indications |
Medically Necessary:
The use of a back-up (second) ventilator in the home setting is considered medically necessary when all of the following criteria are met:
The use of a back-up (second) ventilator in the home setting is considered medically necessary for the following additional indication, when applicable:
Not Medically Necessary:
The use of a back-up (second) ventilator in the home setting is considered not medically necessary when the above criteria are not met.
Coding |
The following codes for treatments and procedures applicable to this document are included below for informational purposes. Inclusion or exclusion of a procedure, diagnosis or device code(s) does not constitute or imply member coverage or provider reimbursement policy. Please refer to the member's contract benefits in effect at the time of service to determine coverage or non-coverage of these services as it applies to an individual member.
When services may be Medically Necessary when criteria are met:
HCPCS |
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E0465 | Home ventilator, any type, used with invasive interface, (e.g., tracheostomy tube) |
E0466 | Home ventilator, any type, used with non-invasive interface, (e.g., mask, chest shell) |
E0467 | Home ventilator, multi-function respiratory device, also performs any or all of the additional functions of oxygen concentration, drug nebulization, aspiration, and cough stimulation, includes all accessories, components and supplies for all functions |
E0468 | Home ventilator, dual-function respiratory device, also performs additional function of cough stimulation, includes all accessories, components and supplies for all functions [when specified as used with a non-invasive interface] |
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| Note: HCPCS modifier ‘-TW’ may be used with the above procedure codes to indicate ‘back-up equipment’. |
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ICD-10 Diagnosis |
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| All diagnoses |
When services are Not Medically Necessary:
For the procedure codes listed above when criteria for a back-up (second) device are not met.
Discussion/General Information |
Mechanical ventilation may be defined as a life support system designed to replace or support normal ventilatory lung function (AARC, 2007). There are a myriad of medical conditions that may cause an individual to require the use of mechanical ventilation for either a short-term or long-term basis. Ventilators can be categorized as either invasive or noninvasive. Invasive mechanical ventilation is defined as the delivery of positive pressure to the lungs via an endotracheal or tracheostomy tube. It is most often used to fully or partially replace the function of spontaneous breathing and gas exchange. Noninvasive ventilation (NIV) may be required part of the time and is delivered through an alternative interface such as a face mask (Hyzy, 2021).
According to the American Association for Respiratory Care (AARC), individuals eligible for invasive long-term mechanical ventilation in the home setting require a tracheostomy tube for ventilatory support, but no longer require intensive medical and monitoring services (AARC, 2007).
The medical necessity criteria in this document for use of back-up ventilators in the home setting are consistent with the recommendations of the AARC Clinical Practice Guidelines for Long-term Invasive Mechanical Ventilation in the Home Setting (AARC, 2007). This document has not been updated since 2007.
References |
Government Agency, Medical Society, and Other Authoritative Publications:
Index |
Ventilators, Back-up in the Home Setting
The use of specific product names is illustrative only. It is not intended to be a recommendation of one product over another, and is not intended to represent a complete listing of all products available.
History |
Status | Date | Action |
Reviewed | 08/08/2024 | Medical Policy & Technology Assessment Committee (MPTAC) review. Revised References section. |
| 06/28/2024 | Updated Coding section, added E0468. |
Revised | 08/10/2023 | MPTAC review. Reformatted bullets to alphanumeric. Updated Reference section. |
Reviewed | 08/11/2022 | MPTAC review. Updated Discussion and Reference sections. |
Reviewed | 08/12/2021 | MPTAC review. Updated Discussion/General Information and References sections. |
Revised | 08/13/2020 | MPTAC review. Updated MN formatting in the Clinical Indications section. Removed written version of number and maintained numeric value in MN Clinical Indications section. Updated Description and References sections. Reformatted Coding section. |
Reviewed | 08/22/2019 | MPTAC review. References were updated. |
| 12/27/2018 | Updated Coding section with 01/01/2019 HCPCS changes; added E0467. |
Reviewed | 09/13/2018 | MPTAC review. References were updated. |
Reviewed | 11/02/2017 | MPTAC review. The document header wording was updated from “Current Effective Date” to “Publish Date.” References were updated. |
Reviewed | 11/03/2016 | MPTAC review. References were updated. |
Reviewed | 11/05/2015 | MPTAC review. References were updated. Updated Coding section with 01/01/2016 HCPCS changes; removed E0450, E0460, E0461, E0463, E0464 deleted 12/31/2015 and also removed ICD-9 codes. |
Reviewed | 11/13/2014 | MPTAC review. References were updated. |
Reviewed | 11/14/2013 | MPTAC review. References were updated. |
Reviewed | 11/08/2012 | MPTAC review. References were updated. |
Reviewed | 11/17/2011 | MPTAC review. References were updated. |
Reviewed | 11/18/2010 | MPTAC review. References were updated. |
Reviewed | 11/19/2009 | MPTAC review. References were updated. |
Reviewed | 11/20/2008 | MPTAC review. References were updated. |
Reviewed | 11/29/2007 | MPTAC review. References were updated. |
Reviewed | 12/07/2006 | MPTAC review. References and coding were updated. |
New | 12/01/2005 | MPTAC initial guideline development. |
Pre-Merger Organizations | Last Review Date | Document Number | Title |
Anthem, Inc. |
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| No document |
Anthem Southeast (Virginia) | 08/10/2004 | Memo 1216 | Back-Up Ventilators in the Home Setting |
WellPoint Health Networks, Inc. |
|
| No document |
This Clinical UM Guideline is intended to provide assistance in interpreting Healthy Blue’s standard Medicaid benefit plan. When evaluating insurance coverage for the provision of medical care, federal, state and/or contractual requirements must be referenced, since these may limit or differ from the standard benefit plan. In the event of a conflict, the federal, state and/or contractual requirements for the applicable benefit plan coverage will govern. Healthy Blue reserves the right to modify its Policies and Guidelines as necessary and in accordance with legal and contractual requirements. This Clinical UM Guideline is provided for informational purposes. It does not constitute medical advice. Healthy Blue may also use tools and criteria developed by third parties, to assist us in administering health benefits. Healthy Blue’s Policies and Guidelines are intended to be used in accordance with the independent professional medical judgment of a qualified health care provider and do not constitute the practice of medicine or medical advice.