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DOI 10.7326/m23-1485

Медицинская библиотека · Annals of internal medicine · 2024

Surgery, Needle Fasciotomy, or Collagenase Injection for Dupuytren Contracture : A Randomized Controlled Trial.

Räisänen Mikko Petteri, Leppänen Olli V, Soikkeli Janne, Reito Aleksi, Malmivaara Antti, Buchbinder Rachelle, Kautiainen Hannu, Kaivorinne Antti, Stjernberg-Salmela Susanna, Lappalainen Minna, Luokkala Toni, Pönkkö Annele, Taskinen Hanna-Stiina, Pääkkönen Markus, Jaatinen Kati, Juurakko Joona, Karjalainen Venla-Linnea, Karjalainen Teemu

Рандомизированное исследованиеМногоцентровое исследованиеСтатьяПоддержка исследования: вне правительства СШАEquivalence TrialПеревод в очереди

Аннотация

BACKGROUND

Surgery, needle fasciotomy, and collagenase injection are used to treat Dupuytren contracture. The treatment decision requires balancing initial morbidity and costs of surgery against its potential long-term benefits over needle fasciotomy and collagenase.

OBJECTIVE

To compare the effectiveness of surgery, needle fasciotomy, and collagenase injection at 3 months and 2 years (secondary time points of the trial).

DESIGN

A multicenter, randomized, outcome assessor-blinded, superiority trial. (ClinicalTrials.gov: NCT03192020).

SETTING

6 public hospitals in Finland.

PARTICIPANTS

302 persons with treatment-naive Dupuytren contracture (contracture angle <135°).

INTERVENTION: Surgery (n = 101), needle fasciotomy (n = 101), or collagenase (n = 100).

MEASUREMENTS: The primary outcome was the success rate, defined as greater than 50% contracture release and patients reaching the patient acceptable symptom state. Secondary outcomes included hand function, pain, quality of life, patient satisfaction, residual contracture angle, finger flexion, risk for retreatment, and serious adverse events.

RESULTS

A total of 292 (97%) and 284 (94%) participants completed the 3-month and 2-year follow-ups. Success rates were similar at 3 months: 71% (95% CI, 62% to 80%) for surgery, 73% (CI, 64% to 82%) for needle fasciotomy, and 73% (CI, 64% to 82%) for collagenase. At 2 years, surgery had superior success rates compared with both needle fasciotomy (78% vs. 50%; adjusted risk difference [aRD], 0.30 [CI, 0.17 to 0.43]) and collagenase (78% vs. 65%; aRD, 0.13 [CI, 0.01 to 0.26]). Secondary analyses paralleled with the primary analysis.

LIMITATION: Participants were not blinded.

CONCLUSION

Initial outcomes are similar between the treatments, but at 2 years success rates were maintained in the surgery group but were lower with both needle fasciotomy and collagenase despite retreatments.

PRIMARY FUNDING SOURCE: Research Council of Finland.

Для цитирования: Räisänen Mikko Petteri, Leppänen Olli V, Soikkeli Janne, Reito Aleksi, Malmivaara Antti, Buchbinder Rachelle, Kautiainen Hannu, Kaivorinne Antti, Stjernberg-Salmela Susanna, Lappalainen Minna, Luokkala Toni, Pönkkö Annele, Taskinen Hanna-Stiina, Pääkkönen Markus, Jaatinen Kati, Juurakko Joona, Karjalainen Venla-Linnea, Karjalainen Teemu. Surgery, Needle Fasciotomy, or Collagenase Injection for Dupuytren Contracture : A Randomized Controlled Trial.. Annals of internal medicine. 2024. DOI: 10.7326/m23-1485.

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