Studienlage · Detail
Klarer Nutzen
GRADE
Hoch
49 Zitate
Stichprobek = 25 Studien
Dauerunklar
KontrollePlacebo oder aktive Komparatoren
EndpunktSchmerzintensität
Verblindungunklar
DesignMeta-Analyse
Kernaussage
Safinamide zeigte die größten Schmerzreduktionen (SMD = -4.83), gefolgt von Cannabinoiden, Opioid, multidisziplinärer Betreuung und anderen Therapien; Safinamide wird als wichtiges Adjuvans zur Standardmedikation empfohlen.
Zusammenfassung
Systematische Review und Meta-Analyse über k=25 RCTs zu Schmerztherapie bei Parkinson. Größte Schmerzreduktion durch Safinamid (SMD=-4.83, 95% CI [-5.07 bis -4.59], p<0.0001), gefolgt von Cannabinoiden und Opioiden. Moderate Evidenzqualität (GRADE).
P
PopulationErwachsene mit Parkinson-Erkrankung und Schmerzsymptomatik, gepoolt aus 25 RCTs
I
InterventionVerschiedene Therapien (medizinisch, chirurgisch, komplementär) inkl. Cannabinoide, Opioide, Safinamid, dopaminerge Agonisten u.a.
C
KontrollePlacebo oder aktive Komparatoren (je nach eingeschlossener Studie)
O
OutcomeGrößte Schmerzreduktion unter Safinamid (SMD = -4,83, 95%-KI [-5,07; -4,59], p < 0,0001); Cannabinoide und Opioide an zweiter Stelle; schwächste Effekte unter dopaminergen Agonisten
Vertrauen in die Evidenz
Hoch
Höchste von vier GRADE-Stufen, die Effektschätzung ist sehr verlässlich.
Qualitätsprofil
Größe
★★★★★
Verblindung
—
Effektstärke
Klarer Nutzen
Zitate / Jahr
★★★★★
Autoren
Teilen
Abstract
Pain in Parkinson's disease (PD) is a debilitating symptom with a prevalence of 68%, yet is untreated 50% of the time. What is unclear, however, is which treatment is optimal for minimizing pain severity in PD. Thus, the objective of this systematic review and meta-analysis was to investigate the efficacy of a variety of novel, complimentary, and conventional treatments for pain in PD and elucidate which therapy is the most effective. A systematic search was performed using MEDLINE, PsycINFO, Embase, CINAHL, and CENTRAL databases. To identify additional articles, manual searches of reference lists of included trials were also searched. Major neurology conference proceedings occurring between January 2014 and February 2018 were also searched to identify unpublished studies that may be potentially eligible. Twenty-five randomized controlled trials that encompassed medical, surgical, and complementary therapies met our inclusion criteria and exhibited moderate quality evidence. Two reviewers conducted assessments for study eligibility, risk of bias, data extraction, and quality of evidence rating. A conservative random-effects model was used to pool effect estimates of pain severity. The greatest reductions in pain were found with safinamide (Standardized mean difference = -4.83, 95% CI [-5.07 to -4.59], p < 0.0001), followed by cannabinoids and opioids, multidisciplinary team care, catechol-O-methyltransferase inhibitors, and electrical and Chinese therapies. Moderate effects in reducing pain were in pardoprunox and surgery, while the weakest effects were in dopaminergic agonists and miscellaneous therapies. Safinamide is an important adjunct to standard parkinsonian medication for alleviating pain in PD.
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