Clinical UM Guideline |
Subject: Home Enteral Nutrition | |
Guideline #: CG-MED-08 | Publish Date: 10/01/2024 |
Status: Revised | Last Review Date: 08/08/2024 |
Description |
This document addresses “medical food” or commercially available processed enteral products (please see the Definitions section for further information regarding medical food) when used in the home to meet basic metabolic needs in a variety of conditions affecting either the mechanical or metabolic process of digestion. Enteral nutrition consists of nutritional support given via the gastrointestinal (GI) tract, either directly or through any of a variety of tubes used in specific medical circumstances. This includes oral feeding, sip feeding, and tube feeding using nasogastric, gastrostomy, jejunostomy, or other tubes. This document does not address standard food (not for medical purposes), although it is technically an enteral nutritional product.
Note: Some benefit plans exclude products available without prescription, sometimes referred to as ‘over the counter’, even when prescribed by a physician or other healthcare provider. Enteral food products are often available without prescription. Please see the text in the footnote of this document regarding Federal and State mandates and contract language, as these documents often specifically address the topic of enteral nutrition.
Note: For criteria related to Relizorb™, refer to applicable guidelines used by the plan.
Note: Please see the following related document for additional information:
Clinical Indications |
I. Oral Enteral Nutrition
Medically Necessary:
Oral enteral nutrition (oral feeding) is considered medically necessary when all of the following criteria are met:
Oral enteral nutrition is considered medically necessary when the product constitutes less than 50 percent of the individual’s caloric intake and either of the following (A or B) are met:
Not Medically Necessary:
Oral enteral nutrition is considered not medically necessary when the criteria above have not been met.
Oral enteral nutrition is considered not medically necessary when use of a product is based on the convenience or preference of the individual or provider.
II. Enteral Nutrition Via Tube
Medically Necessary:
Enteral nutrition via tube feeding is considered medically necessary when either of the following criteria (A or B) are met:
Not Medically Necessary:
Enteral nutrition via tube is considered not medically necessary the criteria above have not been met .
III. Other Considerations
Not Medically Necessary:
The use of formulas and other food products is considered not medically necessary when the criteria above have not been met including, but not limited to:
Continuation of home enteral nutrition, regardless of route of administration, is considered not medically necessary when documentation demonstrates the applicable medical necessity criteria above are no longer 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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B4034 | Enteral feeding supply kit; syringe fed, per day, includes but not limited to feeding/flushing syringe, administration set tubing, dressings, tape |
B4035 | Enteral feeding supply kit; pump fed, per day, includes but not limited to feeding/flushing syringe, administration set tubing, dressings, tape |
B4036 | Enteral feeding supply kit; gravity fed, per day, includes but not limited to feeding/flushing syringe, administration set tubing, dressings, tape |
B4081-B4088 | Nasogastric, stomach, gastrostomy/jejunostomy tubes [includes codes B4081, B4082, B4083, B4087, B4088] |
B4100 | Food thickener, administered orally, per ounce |
B4102 | Enteral formula, for adults, used to replace fluids and electrolytes (e.g., clear liquids), 500 ml = 1 unit |
B4103 | Enteral formula, for pediatrics, used to replace fluids and electrolytes (e.g., clear liquids), 500 ml = 1 unit |
B4104 | Additive for enteral formula (e.g., fiber) |
B4148 | Enteral feeding supply kit; elastomeric control fed, per day, includes but not limited to feeding/flushing syringe, administration set tubing, dressings, tape |
B4149-B4162 | Enteral formula (administered through an enteral feeding tube) [includes codes B4149, B4150, B4152, B4153, B4154, B4155, B4157, B4158, B4159, B4160, B4161, B4162] |
B9002 | Enteral nutrition infusion pump, any type |
S9340-S9343 | Home therapy, enteral nutrition [includes codes S9340, S9341, S9342, S9343] |
S9432 | Medical foods for noninborn errors of metabolism |
S9433 | Medical food nutritionally complete, administered orally, providing 100% of nutritional intake |
S9434 | Modified solid food supplements for inborn errors of metabolism |
S9435 | Medical foods for inborn errors of metabolism |
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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 are not met or for situations designated in the Clinical Indications section as not medically necessary.
Discussion/General Information |
Enteral nutrition is indicated in order to maintain optimal health status for individuals with diseases or structural defects of the GI tract that interfere with transport, digestion or absorption of nutrients. Such conditions may include anatomic obstructions due to cancer, motility disorders such as gastroparesis, or metabolic absorptive disorders such as PKU.
The most optimal route of enteral intake is swallowing by mouth. In conditions where this is not possible, a tube may be placed to facilitate transport of nutrition to the digestive/absorptive sites of the GI tract. Tube placement and types are governed by individual needs; the least invasive approach being placement of a nasogastric tube. Enteral tubes may also be placed percutaneously through an abdominal approach; this is most appropriate for long-term needs due to the reduced risk of aspiration and reflux (CMS NCD for Enteral Nutrition, 1984; Simon, 2000). The American Medical Dietary Association (2015), The American Academy of Hospice and Palliative Medicine (2013) and the American Geriatrics Society (2015) recommend against placement of percutaneous feeding tubes in individuals with advanced dementia; instead, oral assisted feedings should be offered. Advanced dementia, as described in the landmark CASCADE (Choices, Attitudes, and Strategies for Care of Advanced Dementia at the End-of-Life) study, is defined as the following: (1) Cognitive Performance Score (CPS) equal to 5 or 6, (2) cognitive impairment due to dementia (any type), (3) Global Deterioration Scale (GDS) equal to 7 (Mitchell, 2006).
The term Total Enteral Nutrition (TEN) infers that the individual is receiving more than 50% of their daily caloric intake via enteral nutrition products. If fewer than 50% of daily calories are supplied by enteral nutrition products, they are considered supplemental.
Oral enteral formula is needed for individuals with inherited metabolic digestive disorders such as:
These diseases are characterized by inborn errors of amino acid metabolism and have distinctive nutritional requirements. Special formulas are used for the dietary management of these diseases.
The term "medical foods" does not pertain to all foods fed to ill individuals. Medical foods are foods that are specially formulated and processed (as opposed to a naturally occurring foodstuff used in a natural state) for the individual who is seriously ill or who requires the product as a major treatment modality. Medical foods are intended solely to meet the dietary needs of individuals who have specific metabolic or physiological limitations that restrict their ability to digest regular food. According to the Food and Drug Administration (FDA), a product must meet all of the following minimum criteria to be considered a medical food:
The use of weight for a given age is a common metric used to determine if an individual meets criteria for failure to thrive (FTT). However, the threshold for weight for age is not standardized. Cole and colleagues (2011) use “weight less than 75 percent of median weight for age,” while the Agency for Healthcare Research and Quality (AHRQ) report states that the U.S. Social Security Administration (SSA) considers FTT to be present “when there is a fall in weight to below the 3rd percentile or to less than 75% of median weight-for-height or age in children under two years old” (Perrin, 2003). The current SSA language says growth retardation should be documented by 3 measurements over a 6 month period showing “less than the third percentile on the CDC’s [Center for Disease Control’s] most recent weight-for-length charts” for children under the age of 2, and “less than the 3rd percentile on the CDC’s most recent BMI for age growth charts” for children 2 years old and older (SSA, 105.08B1, 24598.002). Cole and colleagues (2011) further illustrate the lack of consensus on this issue by stating:
Other definitions are used commonly in the professional literature such as height-for-weight <3rd percentile; weight-for-age less than 3rd or 5th percentile or less than 80 percent of median for age; weight-for-height <10th percentile; and weight-for-age more than 2 standard deviations below the mean for age.
Both the terms “corrected” age and “chronological” age appear frequently in the literature regarding the measurement of age in children diagnosed with FTT. The use of the term “corrected” allows for greater accuracy in the estimation of expected growth in children, specifically those born premature, who may have a significant discrepancy between their gestational and chronological ages. However, the use of this convention is not uniform in either the literature or guidelines addressing this issue. In accordance with Cole and colleagues (2011), this guideline uses the term “corrected” when referring to the measurement of premature infants.
Cessation of home enteral nutrition therapy may be warranted if the individual is no longer deriving benefit from therapy or in the opinion of the treating provider the risks of enteral treatment outweigh the benefits (Durfee, 2014). Such circumstances may be present when the condition for which the individual has been receiving therapy is no longer present, the individual has been transferred to the facility setting, the individual’s condition has changed such that other nutritional services are needed, and other such circumstances.
Definitions |
Cognitive Performance Score (CPS): A validated score that uses 5 variables from the Minimum Data Set (MDS)20 to group individuals into the following 7 hierarchical cognitive performance categories; 0=intact, 1=borderline intact, 2=mild impairment, 3=moderate impairment, 4=moderately severe impairment, 5=severe impairment, and 6=very severe impairment.
Dysphagia: The term that describes difficulty swallowing due to abnormal swallowing reflex.
Food allergy or hypersensitivity: A clinically abnormal response believed to be caused by an immunologic reaction resulting from the ingestion of a food or food additive.
Food anaphylaxis: A classic allergic hypersensitivity reaction to food or food additives involving IgE antibody that occurs rapidly and may be life threatening.
Food challenge: This is an evaluation technique that may be used to assist in the diagnosis of food or eating-related disorders. After an adequate time with the exclusion of suspected foods (usually a week or two), the suspected food or foods are administered under close supervision in a dose escalation manner with proper observation periods between doses. Food challenges may be done in an open manner with the individual aware of what they are being given, with the individual unaware, or with both the individual and physician unaware.
Global Deterioration Scale (GDS): Classifies dementia into 7 stages (1 to 7) based on broad descriptions of the cognitive and functional deficits that typify each stage. Stage 7 of the GDS is distinguished by the following features: very severe cognitive decline with minimal to no verbal communication, assistance needed to eat and toilet, incontinence of urine and stool, and loss of basic psychomotor skills (for example, may have lost ability to walk).
Medical food: As defined in section 5(b) of the Orphan Drug Act (21 U.S.C. 360ee (b) (3) as:
A food which is formulated to be consumed or administered enterally under the supervision of a physician and which is intended for the specific dietary management of a disease or condition for which distinctive nutritional requirements, based on recognized scientific principles, are established by medical evaluation.*
* U.S. Food and Drug Administration. Regulatory Information. Section 5 of Orphan Drug Act. Available at: http://www.fda.gov/Food/GuidanceRegulation/GuidanceDocumentsRegulatoryInformation/MedicalFoods/default.htm. Accessed on July 25, 2024.
Proximal gastrointestinal tract: The section of the GI tract from the mouth to the small bowel.
Standard food: This is regular grocery products including typical (not specially formulated) infant formulas.
Supplemental nutrition: Fewer than 50% of daily calories are supplied by enteral nutrition products.
Total enteral nutrition (TEN): Individual is receiving more than 50% of their daily caloric intake via enteral nutrition products.
References |
Peer Reviewed Publications:
Government Agency, Medical Society, and Other Authoritative Publications:
Index |
Home Enteral Nutrition
History |
Status | Date | Action |
Revised | 08/08/2024 | Medical Policy & Technology Assessment Committee (MPTAC) review. Revised oral enteral nutrition MN statement to rearrange criterion and update language. Revised enteral nutrition via tube MN statement to align language with first statement section. Revised Definitions and References sections. |
Revised | 08/10/2023 | MPTAC review. Revised enteral nutrition via tube not medically necessary statement. Added treatment cessation criteria. Revised formatting of Clinical Indications section. Revised Discussion and References sections. Updated Coding section with 10/01/2023 HCPCS changes, added B4148. |
Reviewed | 08/11/2022 | MPTAC review. Updated References section. |
Reviewed | 08/12/2021 | MPTAC review. Added a “Note” related to review of Relizorb. Updated References section. Updated Coding section with 10/01/2021 HCPCS changes, added S9432; also removed code B4105 now addressed elsewhere. |
Reviewed | 08/13/2020 | MPTAC review. Updated References section. Reformatted Coding section. |
Reviewed | 08/22/2019 | MPTAC review. Updated Definitions and References section. |
| 12/27/2018 | Updated Coding section with 01/01/2019 HCPCS changes; added B4105. |
Reviewed | 09/13/2018 | MPTAC review. Updated Definitions and References section. |
Reviewed | 11/02/2017 | MPTAC review. Updated header language from “Current Effective Date” to “Publish Date”. Updated References section. |
Revised | 11/03/2016 | MPTAC review. Added advanced dementia to the NMN criteria. Updated Discussion/General Information, Definition and References sections. Updated Coding section with 01/01/2017 HCPCS changes. |
Reviewed | 11/05/2015 | MPTAC review. Updated Discussion/General Information, Definitions, References and Website sections. Removed ICD-9 codes from Coding section. |
Revised | 11/13/2014 | MPTAC review. Clarified Clinical Indications. Updated Description, Discussion/General Information, References and Websites sections. |
Revised | 11/14/2013 | MPTAC review. Changed “chronological age” to “corrected age” in medically necessary criteria for oral enteral nutrition for children with failure to thrive unresponsive to standard age appropriate interventions. Updated Rationale and Reference sections. |
Reviewed | 02/14/2013 | MPTAC review. No change to position statement. |
Reviewed | 02/16/2012 | MPTAC review. No change to position statement. |
Reviewed | 02/17/2011 | MPTAC review. No change to position statement. Updated Reference section. |
| 01/01/2011 | Updated Coding section with 01/01/2011 HCPCS changes. |
Reviewed | 02/25/2010 | MPTAC review. No change to position statement. Updated Reference section. |
Revised | 02/26/2009 | MPTAC review. Modified note in description regarding benefit issues. Reorganized position statement section. Added requirement for documentation of food challenge to oral nutrition medically necessary statement regarding allergy or hypersensitivity to cow or soy milk. Added criteria to oral nutrition medically necessary statement for malabsorption conditions to include “when associated with failure to gain weight or meet established growth expectations.” Added Failure to Thrive as an oral nutrition medically necessary indication. Added statement for when oral or tube nutrition is medically necessary when it comprises less than 50% of intake. Added medically necessary criteria for tube nutrition requiring that individuals must have a condition that either interferes with swallowing or is associated with obstruction of the proximal gastrointestinal tract. Added not medically necessary statement for when used in individuals with normal swallowing and normal proximal gastrointestinal tract function. Updated Discussion, Definitions, and Reference sections. |
| 01/01/2009 | Updated Coding section with 01/01/2009 HCPCS changes. |
Revised | 08/28/2008 | MPTAC review. Added definition of “medical food.” Added the term “medical food” to all clinical indication statements. Added “conditions that interfere with the metabolism of specific nutrients” and other clarifying language to the medically necessary statement in section I. Added “The diagnosis is not failure to thrive” to medically necessary statement in Section II. Added “The diagnosis is not failure to thrive” and “the diagnosis is not allergy to mother’s milk”, and statement addressing continuation of therapy to medically necessary statement In section III. Added not medically necessary statement to section III addressing re-evaluation of therapy, and “The diagnosis is not failure to thrive” and “the diagnosis is not allergy to mother’s milk”. Added “The diagnosis is not failure to thrive” and “the diagnosis is not allergy to mother’s milk” to medically necessary section in Section IV. Added new not medically necessary statement to section IV for when medical food is used primarily for convenience or for individuals with disorders of swallowing where non-medical food is tolerated. Revised Discussion section. Updated Coding section with 10/01/2008 ICD-9 changes. |
Revised | 05/15/2008 | MPTAC review. Revised age criteria for enteral feeding via tube. Reorganized position statement section. Clarified criteria regarding “inborn error of metabolism.” |
Revised | 11/29/2007 | MPTAC review. Added “in all situations” to not medically necessary statement regarding over the counter and specialized pediatric formulas. Updated Reference section. Updated Coding section with 01/01/2008 HCPCS changes. |
| 10/01/2007 | Updated coding section with 10/01/2007 ICD-9 changes. |
Reviewed | 12/07/2006 | MPTAC review. No change to guideline position statement. |
Revised | 12/01/2005 | MPTAC review. Revision based on Pre-merger Anthem and Pre-merger WellPoint Harmonization. |
Pre-Merger Organizations | Last Review Date | Document Number | Title |
Anthem Virginia | 07/29/2002 | VA State Memo 1157 | Medical Foods For Inborn Errors Of Metabolism And Severe Protein Or Soy Allergies |
Anthem MidWest | 02/11/2005 | Anthem Midwest UM Guideline DME-019 | Specialized Pediatric Nutrition |
Anthem Connecticut | 11/23/2004 | CT State UM Guideline | Specialized Pediatric Nutrition Formula |
WellPoint Health Networks, Inc. | 12/04/2004 | 9.06.05 | Home Enteral Nutrition |
Federal and State law, as well as contract language including definitions and specific coverage provisions/exclusions, and Medical Policy take precedence over Clinical UM Guidelines and must be considered first in determining eligibility for coverage. The member's contract benefits in effect on the date that services are rendered must be used. Clinical UM Guidelines, which address medical efficacy, should be considered before utilizing medical opinion in adjudication. Medical technology is constantly evolving, and we reserve the right to review and update Clinical UM Guidelines periodically. Clinical UM guidelines are used when the plan performs utilization review for the subject. Due to variances in utilization patterns, each plan may choose whether or not to adopt a particular Clinical UM Guideline. To determine if review is required for this Clinical UM Guideline, please contact the customer service number on the back of the member's card.
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