Evidence map›Paper›PMID 40831175›Full record

ArticleJournal of neuromuscular diseases2026

Physiotherapeutic management of patients with SMA: A questionnaire-based online survey among physiotherapists within the SMArtCARE network.

Sibylle Vogt, Cornelia Voigt-Müller, Heidi Rochau-Trumpp, Eva Malm, Doris Roland-Schäfer, Gerda Roetmann, Judith van Vugt, Sabine Stein, Janbernd Kirschner, Astrid Pechmann

Abstract read
In one paragraph

Article in Journal of neuromuscular diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Trial
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Sibylle VogtDepartment of Neuropediatrics and Muscle Disorders, Medical Center - University of Freiburg, Freiburg, Germany.
Cornelia Voigt-MüllerDepartment of Neuropediatrics and Muscle Disorders, Medical Center - University of Freiburg, Freiburg, Germany.
Heidi Rochau-TrumppDepartment of Neurology, Medical Center- University of Heidelberg, Heidelberg, Germany.
Eva MalmDepartment of Neurology, Medical Center - University of Munich, Friedrich-Baur-Institut, Munich, Germany.
Doris Roland-SchäferDepartment of Neuropediatrics, Medical Center - University of Tübingen, Tübingen, Germany.
Gerda RoetmannDepartment of Neuropediatrics, Medical Center - University of Göttingen, Göttingen, Germany.
Judith van VugtUniReha GmbH Rehabilitation Children, Köln, Germany.
Sabine SteinDepartment of Neuropediatrics and Muscle Disorders, Medical Center - University of Freiburg, Freiburg, Germany.
Janbernd KirschnerDepartment of Neuropediatrics and Muscle Disorders, Medical Center - University of Freiburg, Freiburg, Germany.
Astrid PechmannDepartment of Neuropediatrics and Muscle Disorders, Medical Center - University of Freiburg, Freiburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesDisease-modifying treatments (DMT) have dramatically changed phenotypes in patients with spinal muscular atrophy (SMA). Because publications regarding standards of care were published before DMTs emerged, detailed recommendations and guidelines for physiotherapeutic management are still lacking. The objective of this study was to map the physiotherapeutic management of patients with SMA within the SMArtCARE network, a disease-specific registry for patients with 5q-SMA with 83 participating centers in Germany, Switzerland, and Austria.

methodsAn online survey using a modified Delphi approach was conducted among physiotherapists with two questionnaire rounds between June 2022 and June 2023. Seven physiotherapeutic experts developed and revised the questionnaires focusing on the main topics of stretching, positioning, mobility and exercise, and chest physiotherapy. The second questionnaire was based on eight different case studies.

resultsThe second questionnaire was sent to 148 participants with a response rate of 28%. Most of the physiotherapists were well experienced in treating SMA patients. There was a strong consensus that home-based stretching should be used in pediatric patients with contractures regardless of their motor function. Muscle strengthening training was considered to be essential for all sitters and for walkers with moderate motor function restriction by a strong consensus. For all patients with respiratory involvement there was a consensus for prophylactic respiratory therapy.

conclusionOur results describe the current physiotherapeutic management and recommendations within the SMArtCARE network. These findings highlight the need for an individualized approach, and the necessity of developing and adjusting existing guidelines.

Indexed as

Muscular Atrophy, SpinalPhysical TherapistsPhysical Therapy ModalitiesAdultAustriaChildDelphi TechniqueFemaleGermanyHumansMaleSurveys and QuestionnairesSwitzerlandchest physiotherapymuscle strengtheningphysiotherapyspinal muscular atrophystretching

Identifiers

PMID40831175
PMCPMC13438990

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.