ACE Report Cover
Dupuytren's contracture: nightly splinting after fasciectomy or dermo-fasciectomy
Translate this  ACE Report Translate this  ACE Report Translate this  ACE Report
Idioma
Download Download Download
Descarregar
Cite this Report Cite this Report Cite this Report
Citar
Add to Favorites Add to Favorites Add to Favorites Remove from Favorites Remove from Favorites Remove from Favorites
+ Favoritos
Translate this  ACE Report Translate this  ACE Report Translate this  ACE Report
Idioma
Download Download Download
Descarregar
Cite this Report Cite this Report Cite this Report
Citar
Add to Favorites Add to Favorites Add to Favorites Remove from Favorites Remove from Favorites Remove from Favorites
+ Favoritos
HAND & WRIST
Dupuytren's contracture: nightly splinting after fasciectomy or dermo-fasciectomy .
Verified
This report has been verified by one or more authors of the original publication.
High Impact
Este estudo foi identificado como tendo um impacto potencialmente elevado. A métrica de Alto Impacto da OE, baseada em IA, estima a influência que um artigo poderá ter, integrando sinais da revista em que foi publicado e do conteúdo científico do próprio artigo. Desenvolvido com recurso ao mais avançado processamento de linguagem natural, o modelo High Impact da OE prevê com maior precisão o desempenho futuro de um estudo em termos de citações do que o fator de impacto da revista por si só. Isto permite o reconhecimento precoce de investigação clinicamente significativa e ajuda os leitores a concentrarem-se nos artigos com maior probabilidade de moldar a prática futura.

OrthoEvidence Journal (OE Journal) - ACE Report

OE Journal. 2014;2(5):16 BMC Musculoskelet Disord. 2011 Jun 21;12:136. doi: 10.1186/1471-2474-12-136

154 patients with Dupuytren's disease were randomized to receive hand therapy either with or without nightly splinting for 6 months following fasciectomy or dermofasciectomy, in order to determine if splinting provided a beneficial effect to patients 1 year postoperatively. Patients were primarily assessed with the Disabilities of the Arm, Hand, and Shoulder questionnaire, and secondarily through total active flexion, total active extension, and patient satisfaction. The results of the study reflected no significant differences between the primary outcome or any of the secondary outcomes, and that there was no beneficial effect of nightly splinting combined with hand therapy.


Detalhes do financiamento da publicação +
Financiamento:
Non-Industry funded
Patrocinador:
Action Medical Research Charity
Conflicts:
None disclosed

Risco de viés

5,5/10

Critérios de notificação

14/20

Índice de Fragilidade

N/A

Was the allocation sequence adequately generated?

Was allocation adequately concealed?

Blinding Treatment Providers: Was knowledge of the allocated interventions adequately prevented?

Blinding Outcome Assessors: Was knowledge of the allocated interventions adequately prevented?

Blinding Patients: Was knowledge of the allocated interventions adequately prevented?

Was loss to follow-up (missing outcome data) infrequent?

Are reports of the study free of suggestion of selective outcome reporting?

Were outcomes objective, patient-important and assessed in a manner to limit bias (ie. duplicate assessors, Independent assessors)?

Was the sample size sufficiently large to assure a balance of prognosis and sufficiently large number of outcome events?

Was investigator expertise/experience with both treatment and control techniques likely the same (ie.were criteria for surgeon participation/expertise provided)?

Sim = 1

Incerto = 0,5

Não relevante = 0

Não = 0

A Avaliação dos Critérios de Relato avalia a transparência com que os autores relatam as caraterísticas metodológicas e do ensaio na publicação. A avaliação está dividida em cinco categorias que são apresentadas de seguida.

3/4

Randomization

2/4

Outcome Measurements

3/4

Inclusion / Exclusion

2/4

Therapy Description

4/4

Statistics

Detsky AS, Naylor CD, O'Rourke K, McGeer AJ, L'Abbé KA. J Clin Epidemiol. 1992;45:255-65

O Índice de Fragilidade é uma ferramenta que auxilia na interpretação de achados significativos, fornecendo uma medida de força para um resultado. O Índice de Fragilidade representa o número de eventos consecutivos que precisam de ser adicionados a um resultado dicotómico para que o resultado deixe de ser significativo. Um número pequeno representa um resultado mais fraco e um número grande representa um resultado mais forte.

Porque é que este estudo era necessário agora?

Dupuytren's disease is commonly treated with fasciectomy or dermofasciectomy. The most appropriate postoperative rehabilitation protocol following these procedures remains controversial. The use of thermoplastic extension splints is advocated by some authors, whereas others have reported negative results with the use of splinting following surgery. Therefore, this study aimed to evaluate the effect of static night splinting in addition to hand therapy compared to hand therapy alone.

Qual era a principal questão de investigação?

Did combined static night splinting with hand therapy following fasciectomy for Dupuytren's disease improve patient-reported function and disability, active range of motion of the digits, patient satisfaction and recurrence rate of contracture compared to hand therapy alone, measured over 1 year postoperatively?

Caraterísticas do estudo +
Population:
154 patients with Dupuytren's disease of one or more digits, requiring surgical intervention (fasciectomy or dermofasciectomy (surgeon preference)). (n=146 completed follow-up)
Intervention:
Splinting group: 77 patients received a custom-made thermoplastic splint, which they were instructed to wear nightly for 6 months following surgery. Splints were designed for static maximal extension of metacarpophalangeal joint (MCPJ) and/or proximal interphalangeal joint (PIPJ), without adding tension to the wound. Splint diaries were given to monitor adherence to treatment. Patients also underwent non-standardized hand therapy postoperatively. (n=71 completed follow-up)
Comparison:
No Splinting group: 77 patients were allocated to not receive splinting following surgery, and receive hand therapy alone. However, it was deemed unethical to withhold splinting if patients in this group developed contracture which did not respond to hand therapy, therefore a priori criteria were developed for 'per protocol' deviations. Criteria for receiving splinting was a net loss in range of motion of 15 degrees or more at the PIPJ or 20 degrees or more at the MCPJ of the operated finger(s) from 1st to 2nd hand therapy session (usually a week apart; onset and frequency of hand therapy sessions was unclear, however). (n=75 completed follow-up)
Outcomes:
Primary outcome assessment was patient-report function and disability using the 30-item Disabilities of the Arm, Shoulder and Hand (DASH) questionnaire. Secondary outcomes included active range of motion of the MCPJ, PIPJ, and distal interphalangeal joint (DIPJ), assessed with a Rolyan finger goniometer, and summed for total active flexion (TAF) and extension (TAE). Patient satisfaction was also assessed on a scale from 0-10.
Methods:
Open-RCT, Pragmatic, Mulitcentre
Time:
12 months. Follow-up of primary and secondary outcomes was conducted at 3, 6, and 12 months postoperatively, with the exception of patient satisfaction, which was assessed at 6 and 12 months.
Quais foram os resultados importantes?
  • A total of 21 patients of the non-splint group received splinting, 8 of which were protocol violations: One patient received splinting by mistake prior to randomization and 7 patients were given splinting at first hand therapy session due to surgeon request. 13 patients developed contractures between first and second hand therapy sessions fitting the per protocol deviation criteria (all at PIPJ).
  • Intention to treat analysis of 12-month outcome assessment of splint group versus no splint group indicated no significant differences in DASH score (Mean 7.0 vs 6.0, Adjusted difference 0.66 (95%CI -2.79 to 4.11), p=0.703), total active flexion (223.8 degrees vs 227.3 degrees, -2.02 (-7.89 to 3.85), p=0.493), total active extension (-32.9 degrees vs -29.6 degrees, 5.11 (-2.23 to 12.55), p=0.172) and patient satisfaction (8.5 vs 8.9, -0.35 (-1.04 to 0.34), p=0.315). Non-significant difference between groups was also reflected in 3 and 6 month assessments.
  • A per-protocol analysis was also performed due to the number of per protocol deviations, as well as to account for patients with adherence to treatment <50% in first 3 months. No statistically significant differences in primary and secondary outcomes were found between groups in 3-, 6- and 12-month assessment of the per-protocol analysis.
  • Adherence to splint wear in the first 3 months of treatment was 74.6% (SD 29.4%) of nights. 12 patients failed to meet the adherence criterion (>50% of nights for first 3 months).
De que é que me devo lembrar mais?

The addition of nightly static splinting to hand therapy in the first 6 months following fasciectomy or dermofascietomy did not significantly improve patient-reported function/disability, range of motion of operated digits, or patient satisfaction compared to hand therapy alone in patients suffering from Dupuytren's disease.

Como é que isto afectará o tratamento dos meus doentes?

The findings of this study suggest that there is no additional benefit to routine nightly splinting in functional and satisfaction outcomes following surgical treatment of Dupuytren's disease; however, patients who develop postoperative contracture, especially in the early postoperative period, should still be treated with splinting.

AVISO LEGAL

O conteúdo desta página destina-se apenas a fins informativos e não pretende substituir o aconselhamento, diagnóstico ou tratamento médico profissional. Se necessitar de tratamento médico, procure sempre o conselho do seu médico ou dirija-se ao serviço de urgência mais próximo. As opiniões, crenças e pontos de vista expressos pelos indivíduos no conteúdo encontrado nesta página não reflectem as opiniões, crenças e pontos de vista da OrthoEvidence.

0 de 4 artigos mensais GRATUITOS desbloqueados
Atingiu o seu limite de 4 visualizações de artigos gratuitos este mês

Aceda à OrthoEvidence por apenas $1,99 por semana.

Mantenha-se ligado às últimas evidências. Cancele a qualquer altura.
  • Avaliações críticas dos mais recentes ensaios clínicos aleatórios de alto impacto e revisões sistemáticas em ortopedia
  • Acesso ao conteúdo do podcast OrthoEvidence, incluindo colaborações com o Journal of Bone and Joint Surgery, entrevistas com cirurgiões reconhecidos internacionalmente e discussões em mesa redonda sobre notícias e tópicos ortopédicos
  • Subscrição do The Pulse, um boletim informativo duas vezes por semana baseado em evidências, concebido para o ajudar a tomar melhores decisões clínicas
Upgrade
Bem-vindo de volta!
Esqueceu-se da palavra-passe?
Comece hoje o seu teste GRATUITO!

A sua conta será afiliada a
e inclui acesso gratuito ao OrthoEvidence


OU
Esqueceu-se da palavra-passe?

OU
Verifique o seu e-mail

Se existir uma conta com o endereço de e-mail fornecido, ser-lhe-á enviado um e-mail de reposição da palavra-passe. Se não vir uma mensagem de correio eletrónico, verifique a sua pasta de spam ou de lixo eletrónico.

Para obter mais assistência, contacte a nossa equipa de apoio.

Inicie sessão para ativar esta funcionalidade

Para aceder a esta funcionalidade, tem de iniciar sessão numa conta OrthoEvidence ativa. Inicie a sessão ou crie uma conta de avaliação GRATUITA.

Traduzir o Relatório ACE

A OrthoEvidence utiliza um serviço de tradução de terceiros para tornar o conteúdo acessível em vários idiomas. Tenha em atenção que, embora sejam feitos todos os esforços para garantir a exatidão, as traduções podem nem sempre ser perfeitas.

Como citar isto ACE Report

OrthoEvidence. Dupuytren's contracture: nightly splinting after fasciectomy or dermo-fasciectomy. OE Journal. 2014;2(5):16. Available from: https://myorthoevidence.com/AceReport/Show/dupuytren-s-contracture-nightly-splinting-after-fasciectomy-or-dermo-fasciectomy

Copie a citação
Inicie sessão para ativar esta funcionalidade

Para aceder a esta funcionalidade, tem de iniciar sessão numa conta OrthoEvidence ativa. Inicie a sessão ou crie uma conta de avaliação GRATUITA.

Funcionalidade de Membro Premium

Para aceder a esta funcionalidade, tem de ter sessão iniciada numa conta Premium da OrthoEvidence.

Partilhe isto ACE Report