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Dupuytren's contracture: nightly splinting after fasciectomy or dermo-fasciectomy
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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
Questo studio è stato identificato come potenzialmente ad alto impatto. La metrica High Impact di OE, guidata dall'AI, stima l'influenza che un articolo potrebbe avere integrando i segnali della rivista in cui è stato pubblicato e il contenuto scientifico dell'articolo stesso. Sviluppato utilizzando un'elaborazione del linguaggio naturale all'avanguardia, il modello High Impact di OE prevede in modo più accurato la futura performance citazionale di uno studio rispetto al solo fattore di impatto della rivista. Ciò consente di riconoscere prima le ricerche clinicamente significative e aiuta i lettori a concentrarsi sugli articoli che hanno maggiori probabilità di influenzare la pratica 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.


Dettagli sul finanziamento della pubblicazione +
Finanziamento:
Non-Industry funded
Sponsor:
Action Medical Research Charity
Conflicts:
None disclosed

Rischio di pregiudizio

5,5/10

Criteri di segnalazione

14/20

Indice di fragilità

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)?

Sì = 1

Incerto = 0,5

Non rilevante = 0

No = 0

La valutazione dei criteri di segnalazione valuta la trasparenza con cui gli autori riportano le caratteristiche metodologiche e sperimentali dello studio all'interno della pubblicazione. La valutazione è suddivisa in cinque categorie che vengono presentate di seguito.

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

L'Indice di Fragilità è uno strumento che aiuta l'interpretazione dei risultati significativi, fornendo una misura della forza di un risultato. L'Indice di Fragilità rappresenta il numero di eventi consecutivi che devono essere aggiunti a un risultato dicotomico per rendere il risultato non più significativo. Un numero piccolo rappresenta un risultato più debole, mentre un numero grande rappresenta un risultato più forte.

Perché questo studio era necessario ora?

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 la domanda di ricerca principale?

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?

Caratteristiche dello studio +
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.
Quali erano i risultati importanti?
  • 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).
Che cosa devo ricordare di più?

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.

Come influenzerà l'assistenza ai miei pazienti?

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.

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Il contenuto di questa pagina è solo a scopo informativo e non intende sostituire la consulenza, la diagnosi o il trattamento medico professionale. Se ha bisogno di cure mediche, si rivolga sempre al suo medico o al pronto soccorso più vicino. Le opinioni, le convinzioni e i punti di vista espressi dalle persone sui contenuti presenti in questa pagina non riflettono le opinioni, le convinzioni e i punti di vista di OrthoEvidence.

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Come citare questo documento 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

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