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Treatment expectations and perception of therapy in adult patients with spinal muscular atrophy receiving nusinersen.
Meyer, Thomas; Maier, André; Uzelac, Zeljko; Hagenacker, Tim; Günther, René; Schreiber-Katz, Olivia; Weiler, Markus; Steinbach, Robert; Weyen, Ute; Koch, Jan Christoph; Kettemann, Dagmar; Norden, Jenny; Dorst, Johannes; Wurster, Claudia; Ludolph, Albert C; Stolte, Benjamin; Freigang, Maren; Osmanovic, Alma; Petri, Susanne; Grosskreutz, Julian; Rödiger, Annekathrin; Griep, Ramona; Gaudlitz, Marcel; Walter, Bertram; Münch, Christoph; Spittel, Susanne.
Afiliação
  • Meyer T; Department of Neurology, Center for ALS, SMA and other Motor Neuron Disorders, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Maier A; Ambulanzpartner Soziotechnologie APST GmbH, Berlin, Germany.
  • Uzelac Z; Department of Neurology, Center for ALS, SMA and other Motor Neuron Disorders, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Hagenacker T; Department of Neurology, University of Ulm, Ulm, Germany.
  • Günther R; Department of Neurology, Universitätsklinikum Essen, Essen, Germany.
  • Schreiber-Katz O; Department of Neurology, Technische Universität Dresden, Universitätsklinikum Carl Gustav Carus, Dresden, Germany.
  • Weiler M; German Center for Neurodegenerative Diseases (DZNE), Research Site Dresden, Dresden, Germany.
  • Steinbach R; Department of Neurology, Hannover Medical School, Hannover, Germany.
  • Weyen U; Department of Neurology, Heidelberg University Hospital, Heidelberg, Germany.
  • Koch JC; Hans Berger Department of Neurology, Jena University Hospital, Jena, Germany.
  • Kettemann D; Department of Neurology, Center for ALS and other Motor Neuron Disorders, Berufsgenossenschaftliches Universitätsklinikum Bergmannsheil, Bochum, Germany.
  • Norden J; Department of Neurology, Universitätsmedizin Göttingen, Göttingen, Germany.
  • Dorst J; Department of Neurology, Center for ALS, SMA and other Motor Neuron Disorders, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Wurster C; Department of Neurology, Center for ALS, SMA and other Motor Neuron Disorders, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Ludolph AC; Department of Neurology, University of Ulm, Ulm, Germany.
  • Stolte B; Department of Neurology, University of Ulm, Ulm, Germany.
  • Freigang M; Department of Neurology, University of Ulm, Ulm, Germany.
  • Osmanovic A; German Center for Neurodegenerative Diseases (DZNE), Research Site Ulm, Ulm, Germany.
  • Petri S; Department of Neurology, Universitätsklinikum Essen, Essen, Germany.
  • Grosskreutz J; Department of Neurology, Technische Universität Dresden, Universitätsklinikum Carl Gustav Carus, Dresden, Germany.
  • Rödiger A; Department of Neurology, Hannover Medical School, Hannover, Germany.
  • Griep R; Department of Neurology, Hannover Medical School, Hannover, Germany.
  • Gaudlitz M; Hans Berger Department of Neurology, Jena University Hospital, Jena, Germany.
  • Walter B; Hans Berger Department of Neurology, Jena University Hospital, Jena, Germany.
  • Münch C; Ambulanzpartner Soziotechnologie APST GmbH, Berlin, Germany.
  • Spittel S; Ambulanzpartner Soziotechnologie APST GmbH, Berlin, Germany.
Eur J Neurol ; 28(8): 2582-2595, 2021 08.
Article em En | MEDLINE | ID: mdl-33960080
ABSTRACT
BACKGROUND AND

PURPOSE:

This was an investigation of treatment expectations and of the perception of therapy in adult patients with 5q-associated spinal muscular atrophy (5q-SMA) receiving nusinersen.

METHODS:

A prospective, non-interventional observational study of nusinersen treatment in adult 5q-SMA patients was conducted at nine SMA centers in Germany. The functional status, treatment expectations and perceived outcomes were assessed using the Amyotrophic Lateral Sclerosis Functional Rating Scale-extended (ALS-FRS-ex), the Measure Yourself Medical Outcome Profile (MYMOP2), the Treatment Satisfaction Questionnaire for Medication (TSQM-9) and the Net Promoter Score (NPS).

RESULTS:

In all, 151 patients were included with a median age of 36 years (15-69 years). SMA type 3 (n = 90, 59.6%) prevailed, followed by type 2 (33.8%) and type 1 (6.6%). In SMA types 1-3, median ALS-FRS-ex scores were 25, 33 and 46 (of 60 scale points), respectively. MYMOP2 identified distinct treatment expectations head verticalization (n = 13), bulbar function (n = 16), arm function (n = 65), respiration (n = 15), trunk function (n = 34), leg function (n = 76) and generalized symptoms (n = 77). Median symptom severity decreased during nusinersen treatment (median observational period 6.1 months, 0.5-16 months) from 3.7 to 3.3 MYMOP2 score points (p < 0.001). The convenience of drug administration was critical (49.7 of 100 TSQM-9 points, SD 22); however, the overall treatment satisfaction was high (74.3, SD 18) and the recommendation rating very positive (NPS +66).

CONCLUSIONS:

Nusinersen was administered across a broad range of ages, disease durations and motor function deficits. Treatment expectations were highly differentiated and related to SMA type and functional status. Patient-reported outcomes demonstrated a positive perception of nusinersen therapy in adult patients with 5q-SMA.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Atrofia Muscular Espinal / Motivação Tipo de estudo: Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Humans / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Atrofia Muscular Espinal / Motivação Tipo de estudo: Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Humans / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article