free mental health logofreementalhealth.comHOMESITE MAPABOUTFAQsPRIVACY   CONTACTS

Services

           powered by powered by google
web    freementalhealth.com

Mental Health Practice Guidelines

National Guideline ClearinghouseThe below guidelines are meant for mental health professionals to use in their clinical practices. Please be aware that there are various authoring organizations. The NGC has summarized these guidelines. Links are provided to the original source within the guideline documents.

Guideline Title

Practice parameters for the dopaminergic treatment of restless legs syndrome and periodic limb movement disorder.

Bibliographic Source(s)

Littner MR, Kushida C, Anderson WM, Bailey D, Berry RB, Hirshkowitz M, Kapen S, Kramer M, Lee-Chiong T, Li KK, Loube DL, Morgenthaler T, Wise M. Practice parameters for the dopaminergic treatment of restless legs syndrome and periodic limb movement disorder. Sleep 2004 May 1;27(3):557-9. [4 references] PubMed

Guideline Status

This is the current release of the guideline.

Disease/Condition(s)

Restless legs syndrome (RLS) and periodic limb movement disorder (PLMD)

Guideline Category

Assessment of Therapeutic EffectivenessTreatment

Clinical Specialty

Family PracticeInternal MedicineNeurologySleep Medicine

Intended Users

Physicians

Guideline Objective(s)

To serve as a guide for the appropriate use of dopaminergic agents in the treatment of restless legs syndrome (RLS) and periodic limb movement disorder (PLMD)

Target Population

Patients with restless legs syndrome (RLS) and periodic limb movement disorder (PLMD)

Interventions and Practices Considered

Levodopa with decarboxylase inhibitor Pergolide Pramipexole Ropinirole Other dopamine agonists including talipexole cabergoline, piribedil, and alpha-dihydroergocryptine Amantadine and selegiline

Major Outcomes Considered

Therapeutic efficacy of dopaminergic agents for treatment of RLS and PLMD Sleep parameters (total sleep time, sleep efficiency) Restless legs syndrome (RLS) and periodic leg movement disorder (PLMD) symptoms Adverse effects Quality of life

Methods Used to Collect/Select Evidence

Hand-searches of Published Literature (Primary Sources) Searches of Electronic Databases

Description of Methods used to Collect/Select the Evidence

Literature searches were first conducted in January 2001, and then updated in August 2001 and finally, April 2002. The search was performed through Medline using the search terms: restless legs, periodic leg movement, periodic limb movement, and nocturnal myoclonus. A PubMed search was also done. Search terms were applied both to the keyword field and as a text search. A total of 227 papers were derived from the searches and reviewed for relevance to the therapeutic literature based on their abstracts. 56 papers were selected for detailed consideration and four were added by task force member recommendation from other search resources. Of these, 27 met the criteria of having a focus on restless legs syndrome (RLS) treatment with a minimum of 5 patients studied, a clear indication of restless legs syndrome or periodic limb movement disorder (PLMD) diagnosis for study entry, and use of a pharmaceutical agent which was primarily active on the dopamine system.

Number of Source Documents

27 articles were identified

Methods Used to Assess the Quality and Strength of the Evidence

Weighting According to a Rating Scheme (Scheme Given)

Rating Scheme for the Strength of the Evidence

Level I (Grade A Recommendation): Large, well-designed, randomized and blinded controlled study with statistically significant conclusions on relevant variables Level II (Grade B Recommendation): Smaller, well-designed, randomized and blinded controlled study with statistically significant conclusions on relevant variables Level III (Grade C Recommendation): Well-designed, non-randomized prospective study with control group Level IV (Grade C Recommendation): Well-designed, large prospective study with historical controls or careful attention to confounding effects or small prospective study with control group Level V (Grade C Recommendation): Small prospective study or case series without control groups

Methods Used to Analyze the Evidence

Systematic Review with Evidence Tables

Description of the Methods Used to Analyze the Evidence

Not stated

Methods Used to Formulate the Recommendations

Expert Consensus

Description of Methods Used to Formulate the Recommendations

In most cases, the conclusions are based on evidence from studies published in peer-reviewed journals that were evaluated as noted in the evidence tables of the companion review paper in the original guideline document. When scientific data are absent, insufficient, or inconclusive, the recommendations are based upon consensus opinion.

Rating Scheme for the Strength of the Recommendations

Standard: This is a generally accepted patient-care strategy, which reflects a high degree of clinical certainty. The term standard generally implies the use of Level I Evidence, which directly addresses the clinical issue, or overwhelming Level II Evidence. Guideline: This is a patient-care strategy, which reflects a moderate degree of clinical certainty. The term guideline implies the use of Level II Evidence or a consensus of Level III Evidence. Option: This is a patient-care strategy, which reflects uncertain clinical use. The term option implies either inconclusive or conflicting evidence or conflicting expert opinion.

Cost Analysis

A formal cost analysis was not performed and published cost analyses were not reviewed.

Method of Guideline Validation

Internal Peer Review

Description of Method of Guideline Validation

These recommendations were developed by the Standards of Practice Committee and reviewed and approved by the Board of Directors of the American Academy of Sleep Medicine.

Major Recommendations

Levels of recommendation (Standard, Guideline, and Option) and levels of evidence (I-V) are defined at the end of the "Major Recommendations" field. Levodopa with decarboxylase inhibitor is effective in the treatment of restless legs syndrome (RLS) and periodic limb movement disorder (PLMD). (Hening et al., 2004; 4.b; Table 3) (Standard) The dopamine agonist pergolide is effective in the treatment of RLS and PLMD. (Hening et al., 2004; 4.c.ii; Table 4) (Standard) The dopamine agonist pramipexole is effective in the treatment of RLS and PLMD. (Hening et al., 2004; 4.c.iii; Table 4) (Guideline) The dopamine agonist ropinirole is effective in the treatment of RLS and PLMD. (Hening et al., 2004; 4.c.iv; Table 4) (Option) Other dopamine agonists (talipexole, cabergoline, piribedil, and alpha-dihydroergocryptine) may be effective in the treatment of RLS or PLMD, but the level of effectiveness of these agonists is not currently established. (Hening et al., 2004; 4.c.v; Table 4) (Option) The dopaminergic agents amantadine and selegiline may be effective in the treatment of RLS and PLMD, but the level of effectiveness of these agents is not currently established. (Hening et al., 2004; 4.d; Table 5) (Option) No specific recommendations can be made regarding dopaminergic treatment of children or pregnant women with RLS or PLMD. (Hening et al., 2004; 5.b) Definitions: Levels of Recommendation Standard: This is a generally accepted patient-care strategy, which reflects a high degree of clinical certainty. The term standard generally implies the use of Level I Evidence, which directly addresses the clinical issue, or overwhelming Level II Evidence. Guideline: This is a patient-care strategy, which reflects a moderate degree of clinical certainty. The term guideline implies the use of Level II Evidence or a consensus of Level III Evidence. Option: This is a patient-care strategy, which reflects uncertain clinical use. The term option implies either inconclusive or conflicting evidence or conflicting expert opinion. Levels of Evidence Level I (Grade A Recommendation): Large, well-designed, randomized, and blinded controlled study with statistically significant conclusions on relevant variables Level II (Grade B Recommendation): Smaller, well-designed, randomized, and blinded controlled study with statistically significant conclusions on relevant variables Level III (Grade C Recommendation): Well-designed, non-randomized prospective study with control group Level IV (Grade C Recommendation): Well-designed, large prospective study with historical controls or careful attention to confounding effects or small prospective study with control group Level V (Grade C Recommendation): Small prospective study or case series without control groups

Clinical Algorithm(s)

None provided

References Supporting the Recommendations

Hening WA, Allen RP, Earley CJ, Picchietti DL, Silber MH. An update on the dopaminergic treatment of restless legs syndrome and periodic limb movement disorder. Sleep 2004 May 1;27(3):560-83. [88 references] PubMed

Type of Evidence supporting the Recommendations

The type of evidence is specifically stated for each recommendation (See "Major Recommendations" field).

Potential Benefits

Appropriate use of dopaminergic agents in the treatment of restless legs syndrome (RLS) and periodic limb movement disorder (PLMD) Relief of RLS and PLMD symptoms Reduction of PLMS and PLMS-Waking Index Improvement in sleep parameters

Potential Harms

Levodopa with Decarboxylase Inhibitor The main side effects complicating the use of this agent in clinical series are the high frequencies of restless legs syndrome (RLS) daytime augmentation (i.e., occurrence or worsening of daytime RLS symptoms with long-term medication usage, typically increased by higher doses) and early morning rebound of RLS symptoms, especially at higher dose levels. Pergolide Adverse effects include nausea, congestion, and mild augmentation. In most cases, these adverse effects were either minor or could be adequately controlled; however, the development of pleuropulmonary fibrosis or cardiac valvulopathy has been reported in isolated case reports. Pramipexole The most common reported side effects in these studies were fluid retention/edema, daytime fatigue/sleepiness, gastrointestinal distress, insomnia/alertness, dizziness, and occasional augmentation of RLS. Amantadine In one study, side effects of drowsiness and fatigue were reported.

Qualifying Statements

These practice parameters define principles of practice that should meet the needs of most patients in most situations. These guidelines should not, however, be considered inclusive of all proper methods of care or exclusive of other methods of care reasonably directed toward obtaining the same results. The ultimate judgment regarding the propriety of any specific care must be made by the physician in light of the individual circumstances presented by the patient and the available diagnostic and treatment options. These practice parameters reflect the state of knowledge at the time of development and will be reviewed, updated, and revised, as new information becomes available.

Description of Implementation Strategy

An implementation strategy was not provided.

IOM Care Need

Getting BetterLiving with Illness

IOM Domain

Effectiveness

Bibliographic Source(s)

Littner MR, Kushida C, Anderson WM, Bailey D, Berry RB, Hirshkowitz M, Kapen S, Kramer M, Lee-Chiong T, Li KK, Loube DL, Morgenthaler T, Wise M. Practice parameters for the dopaminergic treatment of restless legs syndrome and periodic limb movement disorder. Sleep 2004 May 1;27(3):557-9. [4 references] PubMed

Adaptation

Not applicable: The guideline was not adapted from another source.

Date Released

2004 May 1

Guideline Developer(s)

American Academy of Sleep Medicine - Professional Association

Source(s) of Funding

American Academy of Sleep Medicine

Guideline Committee

Standards of Practice Committee

Composition of Group that Authored the Guideline

Committee Members: Michael R. Littner, MD, VA Greater Los Angeles Healthcare System and David Geffen School of Medicine at UCLA, Sepulveda, CA; Clete Kushida, MD, PhD, Stanford University Center of Excellence for Sleep Disorders, Stanford, CA; W. McDowell Anderson, MD, College of Medicine, University of South Florida, Tampa, FL; Dennis Bailey, DDS, Englewood, Colorado; Richard B. Berry, MD, Malcom Randall VAMC/Univ. of Florida-Gainesville,Fla; Max Hirshkowitz, PhD, Baylor College of Medicine and VA Medical Center, Houston, TX; Sheldon Kapen, MD, VA Medical Center and Wayne State University, Detroit, MI; Milton Kramer, MD, Maimoides Medical Center, Psychiatry Department, Brooklyn, NY and New York University School of Medicine, New York, NY; Teofilo Lee-Chiong, MD, National Jewish Medical and Research Center, Sleep Clinic, Denver, CO; Kasey K. Li, DDS, MD, Stanford Sleep Disorders Clinic and Research Center; Daniel L. Loube, MD, Sleep Medicine Institute, Swedish Medical Center, Seattle, WA; Timothy Morgenthaler, MD, Mayo Sleep Disorders Center, Mayo Clinic, Rochester, MN; Merrill Wise, MD, Departments of Pediatrics and Neurology, Baylor College of Medicine, Houston, TX

Financial Disclosures/Conflicts of Interest

All authors of the accompanying review paper, members of the Standards of Practice Committee, and the American Academy of Sleep Medicine (AASM) Board of Directors completed detailed conflict-of-interest statements and were found to have none with regard to this subject.

Guideline Status

This is the current release of the guideline.

Guideline Availability

Electronic copies: Available in Portable Document Format (PDF) from the American Academy of Sleep Medicine (AASM) Web site. Print copies: Available from the Standards of Practice Committee, American Academy of Sleep Medicine, One Westbrook Corporate Center, Suite 920, Westchester, IL 60154. Web site: www.aasmnet.org.

Availability of Companion Documents

The following is available: Hening WA, Allen RP, Earley CJ, Picchietti DL, Silber MH; Restless Legs Syndrome Task Force of the Standards of Practice Committee of the American Academy of Sleep Medicine. An update on the dopaminergic treatment of restless legs syndrome and periodic limb movement disorder. Sleep 2004 May;27(3):560-83. Electronic copies: Available in Portable Document Format (PDF) from the American Academy of Sleep Medicine Web site. Print copies: Available from the Standards of Practice Committee, American Academy of Sleep Medicine, One Westbrook Corporate Center, Suite 920, Westchester, IL 60154. Web site: www.aasmnet.org.

Patient Resources

None available

NGC STATUS

This NGC summary was completed by ECRI on May 2, 2005. The information was verified by the guideline developer on June 2, 2005.

COPYRIGHT STATEMENT

This NGC summary is based on the original guideline, which is subject to the guideline developer's copyright restrictions. Please contact the American Academy of Sleep Medicine (AASM) for information regarding reproduction of AASM guidelines.

NGC Disclaimer

The National Guideline Clearinghouse™ (NGC) does not develop, produce, approve, or endorse the guidelines represented on this site.All guidelines summarized by NGC and hosted on our site are produced under the auspices of medical specialty societies, relevant professional associations, public or private organizations, other government agencies, health care organizations or plans, and similar entities.Guidelines represented on the NGC Web site are submitted by guideline developers, and are screened solely to determine that they meet the NGC Inclusion Criteria which may be found at http://www.guideline.gov/about/inclusion.aspx.NGC, AHRQ, and its contractor ECRI make no warranties concerning the content or clinical efficacy or effectiveness of the clinical practice guidelines and related materials represented on this site. Moreover, the views and opinions of developers or authors of guidelines represented on this site do not necessarily state or reflect those of NGC, AHRQ, or its contractor ECRI, and inclusion or hosting of guidelines in NGC may not be used for advertising or commercial endorsement purposes.Readers with questions regarding guideline content are directed to contact the guideline developer.