The influence of physiotherapy intervention on patients with multiple sclerosis-related spasticity treated with nabiximols (THC:CBD oromucosal spray).
Grimaldi et al.·PloS oneImpact 2.8
Klarer NutzenGRADEModerat11 Zitate
Stichproben = 290 Pat.
Dauer12 Wochen
KontrolleNabiximols ohne Physiotherapie
EndpunktNRS
Verblindungn.a.
DesignKohortenstudie
Cannabinoidkombination
THC:CBD1:1
Applikationoromukosal
”Kernaussage
Nabiximols reduzierte MS-bedingte Spastizität messbar (NRS von 7,6 auf 5,5), und Physiotherapie verbesserte die klinisch relevante Ansprechrate und Persistenz der Behandlung.
Zusammenfassung
Multizentrische Real-World-Studie n=290 MS-Patienten mit moderater bis schwerer Spastik, Nabiximols (THC:CBD-Spray) + Physiotherapie (PT) vs. ohne PT, 12-Wochen-Follow-up. Mittlere NRS-Reduktion: 7,6 (T0) → 5,8 (T1, 4 Wochen) → 5,5 (T2, 12 Wochen). T1: 77% erreichten ≥20% Verbesserung (IR), 22% ≥30% (CRR). PT-Gruppe: höhere Wahrscheinlichkeit für CRR (OR=2,6; 95% CI 1,3–5,6; p=0,01). Therapieabbruch: 10,3% bei T1, 24,5% bei T2; PT reduzierte späte Abbrüche (HR=0,41; 95% CI 0,23–0,69; p=0,001).
P
PopulationErwachsene mit moderater bis schwerer MS-bedingter Spastik, n=290 (Abschluss Follow-up)
I
InterventionNabiximols (THC:CBD oromukosales Spray, Sativex) als Add-on-Therapie, teils kombiniert mit Physiotherapie
C
KontrolleNabiximols ohne Physiotherapie
O
OutcomeKlinisch relevante Responserate (≥30% NRS-Verbesserung) bei T1 höher mit Physiotherapie (OR=2,6; 95% CI 1,3–5,6; p=0,01); reduzierte Abbruchwahrscheinlichkeit bei Physiotherapie (HR=0,41; 95% CI 0,23–0,69; p=0,001)
Vertrauen in die Evidenz
Sehr niedrigNiedrigModeratHoch
Moderat
Dritte von vier GRADE-Stufen, die Effektschätzung ist wahrscheinlich verlässlich.
Qualitätsprofil
Größe★★★★★
Verblindung—
EffektstärkeKlarer Nutzen
Zitate / Jahr★★★★★
Autoren
Grimaldi AE, De Giglio L, Haggiag S, Bianco A, Cortese A, Crisafulli SG, Monteleone F, Marfia G, Prosperini L, Galgani S
Background: Nabiximols (THC/CBD Oromucosal Spray, Sativex) is used as an add-on therapy to treat moderate to severe spasticity of Multiple Sclerosis (MS).
Objectives: To examine the impact of physiotherapy (PT) programs on effectiveness and persistence of nabiximols treatment in people with MS-related spasticity.
Methods: This is an observational multicenter study with a follow-up period of 12 weeks, conducted in routine care settings in Italy. Patients with moderate to severe MS-related spasticity who started nabiximols were included. Spasticity was evaluated by the patient-rated 0-10 numerical rating scale (NRS). Clinical data were collected at baseline (T0), 4 weeks (T1) and 12 weeks (T2) months after enrollment.
Results: A total of 297 MS patients were selected, 290 completed the 3 months follow-up period. Mean NRS scores were 7.6 +/- 1.1 at T0, 5.8 +/- 1.4 at T1 and 5.5 +/- 1.5 at T2. At T1, 77% of patients reached >/=20% improvement (initial response, IR); 22% reached >/=30% improvement (clinically relevant response, CRR). At T1, patients undergoing PT had a higher probability to reach CRR (Odds Ratio = 2.6 95% CI 1.3-5.6, p = 0.01). Nabiximols was discontinued in 30/290 (10.3%) patients at T1 (early discontinuers) and in 71/290 (24.5%) patients at T2 (late discontinuers). The probability of being late discontinuers was reduced in patients undergoing PT (Hazard Ratio = 0.41; 95% CI 0.23-0.69, p = 0.001).
Conclusions: Our real-life study confirms nabiximols' effectiveness in MS-related spasticity and suggests that the association of a PT program may improve overall response and persistence to nabiximols treatment.