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Outcomes and Early Recurrence Following Enzymatic (Collagenase) Treatment of Moderate and Severe Dupuytren Contractures.
David, Michael; Smith, Gemma; Pinder, Richard; Craigen, Michael; Waldram, Michael; Mishra, Anuj; Dickson, David; Wu, Feiran; Brewster, Mark.
Afiliación
  • David M; Birmingham Hand Centre, The Royal Orthopaedic Hospital, Northfields, Birmingham, West Midlands, United Kingdom. Electronic address: michaeldavid@nhs.net.
  • Smith G; Birmingham Hand Centre, The Royal Orthopaedic Hospital, Northfields, Birmingham, West Midlands, United Kingdom.
  • Pinder R; Birmingham Hand Centre, The Royal Orthopaedic Hospital, Northfields, Birmingham, West Midlands, United Kingdom.
  • Craigen M; Birmingham Hand Centre, The Royal Orthopaedic Hospital, Northfields, Birmingham, West Midlands, United Kingdom.
  • Waldram M; Birmingham Hand Centre, The Royal Orthopaedic Hospital, Northfields, Birmingham, West Midlands, United Kingdom.
  • Mishra A; Birmingham Hand Centre, The Royal Orthopaedic Hospital, Northfields, Birmingham, West Midlands, United Kingdom.
  • Dickson D; Birmingham Hand Centre, The Royal Orthopaedic Hospital, Northfields, Birmingham, West Midlands, United Kingdom.
  • Wu F; Birmingham Hand Centre, The Royal Orthopaedic Hospital, Northfields, Birmingham, West Midlands, United Kingdom.
  • Brewster M; Birmingham Hand Centre, The Royal Orthopaedic Hospital, Northfields, Birmingham, West Midlands, United Kingdom.
J Hand Surg Am ; 45(12): 1187.e1-1187.e11, 2020 Dec.
Article en En | MEDLINE | ID: mdl-32861504
ABSTRACT

PURPOSE:

We offer collagenase Clostridium histolyticum (CCH) injections to all patients with a Dupuytren contracture and a palpable cord. We assessed whether more severe contractures respond less well or recur more frequently.

METHODS:

From a database of 502 CCH injections, 386 (77%) had a complete dataset with minimum 1-year face-to-face follow-up. Contracture severity was assessed using the Tubiana system grade 1 (27%), grade 2 (49%), grade 3 (19%), and grade 4 (5%). Patients received a single intralesional injection of 0.58 mg CCH followed by manipulation. Finger position was measured at 6 to 12 weeks, 6 months, and 1 year. Failure to break the cord, skin tears, and any adverse events were noted. Recurrence was defined as a failure to maintain any prior correction to within 20°.

RESULTS:

There were 17 failures (4%) and 6 allergic reactions (1%). We found 31% corrected completely, with approximately half remaining corrected at 1 year. We achieved 43° (95% confidence interval, 40°-46°) correction of combined deformity, with 11° (95% confidence interval, 9°-13°) correction attrition over 1 year. Sixteen percent of treated digits experienced a recurrence with no difference between Tubiana grades, and one-third chose further treatment. Following treatment, Tubiana grade 1 contractures improved by 78% in comparison with higher grade contractures (55%-67% relative correction). By 1 year, all grades had a similar mean 46% relative correction. A complete correction was seen in 61% of grade 1 contractures, with more severe contractures less likely to correct completely (9%-24%). A 31% skin tear rate had no impact on outcome, recurrence, or long-term morbidity.

CONCLUSIONS:

CCH may treat any Dupuytren cord regardless of severity. Although contracture may recur, few patients pursue further treatment within 1 year. TYPE OF STUDY/LEVEL OF EVIDENCE Therapeutic IV.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Contractura de Dupuytren Límite: Humans Idioma: En Revista: J Hand Surg Am Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Contractura de Dupuytren Límite: Humans Idioma: En Revista: J Hand Surg Am Año: 2020 Tipo del documento: Article
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