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Practice parameters for the dopaminergic treatment of restless legs syndrome and periodic limb movement disorder.
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
This is the current release of the guideline.
Restless legs syndrome (RLS) and periodic limb movement disorder (PLMD)
Assessment of Therapeutic EffectivenessTreatment
Family PracticeInternal MedicineNeurologySleep Medicine
Physicians
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)
Patients with restless legs syndrome (RLS) and periodic limb movement disorder (PLMD)
Levodopa with decarboxylase inhibitor Pergolide Pramipexole Ropinirole Other dopamine agonists including talipexole cabergoline, piribedil, and alpha-dihydroergocryptine Amantadine and selegiline
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
Hand-searches of Published Literature (Primary Sources) Searches of Electronic Databases
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.
27 articles were identified
Weighting According to a Rating Scheme (Scheme Given)
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
Systematic Review with Evidence Tables
Not stated
Expert Consensus
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.
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.
A formal cost analysis was not performed and published cost analyses were not reviewed.
Internal Peer Review
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.
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
None provided
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
The type of evidence is specifically stated for each recommendation (See "Major Recommendations" field).
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
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.
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.
An implementation strategy was not provided.
Getting BetterLiving with Illness
Effectiveness
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
Not applicable: The guideline was not adapted from another source.
2004 May 1
American Academy of Sleep Medicine - Professional Association
American Academy of Sleep Medicine
Standards of Practice Committee
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
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.
This is the current release of the guideline.
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.
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.
None available
This NGC summary was completed by ECRI on May 2, 2005. The information was verified by the guideline developer on June 2, 2005.
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