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Sunflower Health Plan Hyperhidrosis Treatments (PDF) Form


Iontophoresis (electrophoresis, Drionic device)

Indications

(357256) Is the diagnosis primary hyperhidrosis? 
(357257) Has medical complications arisen such as skin maceration with secondary infections, or a significant disruption of professional and/or social life due to excessive sweating? 
(357258) Is the patient unresponsive or unable to tolerate prescribed pharmacotherapies for excessive sweating such as anticholinergics, beta-blockers, or benzodiazepines? 
(357259) Has the patient failed a six-month trial of conservative management including aluminum chloride hexahydrate [Drysol] application, or have topical agents resulted in severe rash? 

Contraindications

(357260) Does the patient have a cardiac pacemaker? 
YesNoN/A
YesNoN/A
YesNoN/A

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Effective Date

NA

Last Reviewed

01/23

Original Document

  Reference



Hyperhidrosis is defined as excessive sweating beyond a level required to maintain normal body temperature in response to heat exposure or exercise. Refer to CP.PHAR.230 AbobotulinumtoxinA (Dysport) Refer to CP.PHAR.232 OnabotulinumtoxinA (Botox) Refer to CP.PMN.177 Qbrexza (glycopyrronium) for requests for glycopyrronium Policy/Criteria I. It is the policy of health plans affiliated with Centene Corporation® that treatment with iontophoresis (electrophoresis, Drionic device) is medically necessary when all of the following criteria are met: A. Diagnosis of primary hyperhidrosis; B. Development of medical complications, such as skin maceration with secondary skin infections or has a significant constant disruption of professional and/or social life (e.g., recurrent changing of clothes, affecting job/social function, etc.) which has occurred because of excessive sweating; C. Unresponsive or unable to tolerate at least one of the pharmacotherapies prescribed for excessive sweating (e.g., anticholinergics, beta-blockers, or benzodiazepines); D. Failed a six-month trial of conservative management including the adherent application of aluminum chloride hexahydrate [Drysol by prescription] or topical agents have resulted in a severe rash; E. Has none of the following contraindications: 1. Cardiac pacemaker; 2. Cardiac arrhythmias; 3. Pregnancy (hyperhidrosis often improves during pregnancy); 4. Metal implants, depending on size and position (may divert the electric current); 5. Cracked skin near the treatment area. II. It is the policy of health plans affiliated with Centene Corporation® that endoscopic thoracic sympathectomy (ETS) for palmar or palmar and axillary hyperhidrosis is medically necessary when all of the following criteria are met: A. Meets all of the iontophoresis criteria in I.A.-D.; B. Has a resting heart rate > 55 beats per minute; C. Hyperhidrosis symptoms started at an early age (usually < 16 years), and surgery is requested for a young member/enrollee (usually < 25 years of age); D. Body mass index < 28; E. Reports no sweating during sleep; F. The member/enrollee has no significant comorbidities; G. Has persistent and severe primary hyperhidrosis; Page 1 of 7 CLINICAL POLICY Hyperhidrosis Treatments H. Has failed one of the following: 1. Iontophoresis; 2. Trial of botulinum toxin for predominantly axillary hyperhidrosis. III.It is the policy of health plans affiliated with Centene Corporation® that surgical excision of axillary sweat glands for axillary hyperhidrosis are medically necessary when all of the following criteria are met: A. Meets all of the iontophoresis criteria in I.A. through D.; B. Has persistent and severe primary hyperhidrosis; C. Has failed one of the following: 1. Iontophoresis; 2. Trial of botulinum toxin. Note: The normal line of medical therapy is: 1. Drysol, then Botox or topical glycopyrronium for axillary hyperhidrosis; 2. Drysol, then iontophoresis for palmoplantar hyperhidrosis; 3. Other treatments are third-line therapies (iontophoresis and surgery for axillary hyperhidrosis, and Botox and surgery for palmoplantar hyperhidrosis). IV. There is insufficient evidence in published peer-reviewed literature to support all other treatments for hyperhidrosis, including, but not limited to, microwave therapy, or liposuction as the sole method of removing axillary sweat glands. Background Hyperhidrosis can be classified as either primary or secondary.12 Primary focal hyperhidrosis is idiopathic in nature and is defined as excessive sweating induced by sympathetic hyperactivity in selected areas that is not associated with an underlying disease process.3 The most common locations are underarms (axillary hyperhidrosis), hands (palmar hyperhidrosis), and feet (plantar hyperhidrosis). Primary focal hyperhidrosis is a condition that is characterized by visible, excessive sweating of at least six months’ duration without apparent cause. Hyperhidrosis can ruin clothing, produce emotional distress, and lead to occupational disability.12 Secondary hyperhidrosis can result from a variety of drugs, such as tricyclic antidepressants, selective serotonin reuptake inhibitors (SSRIs), or underlying diseases/conditions, such as febrile diseases, diabetes mellitus, or menopause. Secondary hyperhidrosis is usually generalized or craniofacial sweating. Secondary gustatory hyperhidrosis is excessive sweating on ingesting highly spiced foods. This trigeminovascular reflex typically occurs symmetrically on scalp or face and predominately over forehead, lips, and nose. Secondary facial gustatory sweating, in contrast, is usually asymmetrical and occurs independently of the nature of the ingested food. This phenomenon frequently occurs after injury or surgery in the region of the parotid gland. A variety of therapies have been investigated for primary hyperhidrosis, including topical therapy with aluminum chloride, iontophoresis, intradermal injections of botulinum toxin type A, endoscopic transthoracic sympathectomy, and surgical excision of axillary sweat glands.1,2,12 Endoscopic thoracic sympathectomy (ETS) is an invasive procedure intended to arrest the symptoms of hyperhidrosis and involves interrupting the upper thoracic sympathetic chain through clipping, cauterization, or cutting.12 Treatment of secondary hyperhidrosis focuses on the Page 2 of 7 CLINICAL POLICY Hyperhidrosis Treatments treatment of the underlying cause, such as discontinuing certain drugs or hormone replacement therapy as a treatment of menopausal symptoms. Microwave energy has been proposed for the treatment of primary axillary hyperhidrosis. The miraDry System (Mirimar Labs, Inc) is a Food and Drug Administration (FDA) approved device indicated for treatment of primary axillary hyperhidrosis. It is not indicated for treating hyperhidrosis related to other body areas or generalized hyperhidrosis. Evidence is still emerging in the published peer-reviewed literature to support the safety and efficacy of microwave energy for the treatment of primary axillary hyperhidrosis.17 Coding Implications This clinical policy references Current Procedural Terminology (CPT®). CPT® is a registered trademark of the American Medical Association. All CPT codes and descriptions are copyrighted 2021, American Medical Association. All rights reserved. CPT codes and CPT descriptions are from the current manuals and those included herein are not intended to be all-inclusive and are included for informational purposes only. Codes referenced in this clinical policy are for informational purposes only. Inclusion or exclusion of any codes does not guarantee coverage. Providers should reference the most up-to-date sources of professional coding guidance prior to the submission of claims for reimbursement of covered services. CPT® Codes 11450 11451 Excision of skin and subcutaneous tissue for hidradenitis, axillary; with simple or intermediate repair Excision of skin and subcutaneous tissue for hidradenitis, axillary; with complex repair Suction assisted lipectomy; trunk Suction assisted lipectomy; upper extremity Thoracoscopy, surgical; with thoracic sympathectomy Sympathectomy, sympathetic nerves 15877* 15878* 32664 64802 through 64823 97024* Application of a modality to 1 or more areas; diathermy (eg, microwave) 97033 * Insufficient evidence in published peer-reviewed literature to support suction assisted liposuction as the sole method of removing axillary sweat glands. Application of a modality to 1 or more areas; iontophoresis, each 15 minutes Reviews, Revisions, and Approvals Policy Developed. Specialist review. Removed all surgical treatments except ETS and excision of sweat glands Updated coding implications. Removed Botox and Dysport from policy, refer to CP.PHAR.09 Botulinum Toxins. Policy converted to new template. References reviewed and updated. Revision Date 04/13 04/14 Approval Date 05/13 05/14 04/15 04/15 04/16 04/16 Page 3 of 7 CLINICAL POLICY Hyperhidrosis Treatments Reviews, Revisions, and Approvals Added microwave therapy for treatment of hyperhidrosis as investigational. Specified in I.A. and II.B. that diagnosis must be primary hyperhidrosis. References reviewed and updated. ICD 10 codes added. Changed I.B from “job/social promotion” to “job/social function.” References reviewed and updated. Separated criteria for ETS and removal of axillary sweat glands, and specified that they meet criteria for iontophoresis A-D. For ETS, added criteria that member heart rate is ≥ 55 beats per minute, symptoms started before 16 years of age, and surgery is on a member less than 25 years of age, that there be no significant comorbidities, that there is no night sweating, and BMI < 28, per 2011 guidelines. Added topical glycopyrronium to normal line of medical therapy for axillary hyperhidrosis, in the note under III. References reviewed and updated. Removed informational codes for chemical denervation of sweat glands: 64560, 64563. Added codes 11450 and 11451. Section IV: Added liposuction as the sole method of removing axillary sweat glands as investigational. Specialist reviewed. Combined criteria points in II. H. and III. C to read “failed one of the following: 1. Iontophoresis or 2. Trial of botulinum toxin.” References reviewed and updated. Replaced “members” with “members/enrollees” in all instances. Annual review. References reviewed and updated. Reviewed by specialist. Changed "Last Review Date" in the header to "Date of Last Revision" and "Date" in revision log to "Revision Date". “Experimental/investigational” verbiage replaced in policy statement and background with descriptive language. Updated reference to CP.PHAR.09 to CP.PHAR.230 and CP.PHAR.232 as well as CP.PMN.117 to CP.PMN.177. Annual review. Updated Criteria II.B. to greater than 55 beats per minute. Removed “is relatively healthy” in criteria II.F. Background updated with no impact on criteria. ICD-10 codes removed. References reviewed and updated. Revision Date 04/17 Approval Date 04/17 02/18 02/18 06/18 06/18 01/19 02/19 11/19 12/19 01/20 12/20 01/21 01/22 1/22 01/23 01/23