CC BY-NC-ND 4.0 · Rev Bras Ortop (Sao Paulo) 2021; 56(04): 478-484
DOI: 10.1055/s-0040-1721839
Artigo Original
Mão

Epidemiology of Dupuytren disease and Patients Undergoing Selective Fasciectomy[*]

Article in several languages: português | English
1   Centro de Cirurgia da Mão, Instituto Nacional de Traumatologia e Ortopedia, Rio de Janeiro, RJ, Brasil
,
2   Divisão de Pesquisa, Instituto Nacional de Traumatologia e Ortopedia, Rio de Janeiro, RJ, Brasil
3   Unidade de Farmácia, Centro Universitário Estadual da Zona Oeste, Rio de Janeiro, RJ, Brasil
,
1   Centro de Cirurgia da Mão, Instituto Nacional de Traumatologia e Ortopedia, Rio de Janeiro, RJ, Brasil
,
2   Divisão de Pesquisa, Instituto Nacional de Traumatologia e Ortopedia, Rio de Janeiro, RJ, Brasil
,
2   Divisão de Pesquisa, Instituto Nacional de Traumatologia e Ortopedia, Rio de Janeiro, RJ, Brasil
,
2   Divisão de Pesquisa, Instituto Nacional de Traumatologia e Ortopedia, Rio de Janeiro, RJ, Brasil
› Author Affiliations
 

Abstract

Objective To describe the epidemiological and clinical profile of patients with Dupuytren disease treated by selective fasciectomy and the factors associated with the severity of the disease.

Methods Retrospective descriptive observational study involving 247 patients with Dupuytren disease, from 2013 to 2019. Multivariate logistic regression was performed for data analysis.

Results Most patients were male (83.8%), self-declared white (65.2%), alcoholics (59.6%) and 49% were smokers, with a mean age of 66 ± 9 years old, with 77.2% presenting symptoms of the disease after the age of 51 years old. Approximately 51.9, 29.6 and 17.3%, respectively, had arterial hypertension, diabetes mellitus and dyslipidemia comorbidities. Bilateral involvement of the hands was observed in 73.3% of the patients. The rate of intra- and post-selective fasciectomy complications was of 0.6 and 24.3%, respectively, with 5.2% of the patients needing reintervention after 1 year of follow-up. After multivariate analysis, males were associated with bilateral involvement of the hands (odds ratio [OR] = 2.10; 95% confidence interval [CI]: 1.03–4.31) and with a greater number of affected rays (OR = 3.41; 95% CI: 1.66–7.03). Dyslipidemia was associated with reintervention (OR = 5.7; 95% CI = 1.03–31.4) and bilaterality with a higher number of complications (35.7 versus 19.7%).

Conclusion A low rate of reintervention and operative complications was observed in patients with Dupuytren disease treated by selective fasciectomy. Male gender was associated with severe disease (bilaterality and more than two affected rays), and dyslipidemia with reintervention.


#

Introduction

Dupuytren disease or contracture figures among the most common human connective tissue disorders.[1] It is characterized by a progressive, irreversible fibroblast proliferation affecting the palmar fascia, resulting in its gradual thickening, which causes a flexion contraction of the fingers.[2] Initially, it presents as subcutaneous nodules, followed by fibrous cords, which account for contractures.[3]

The incidence of Dupuytren disease ranges from 3 to 40%. It often affects males[4] > 50 years old, with a higher prevalence in Caucasians.[5] In addition, its incidence is high among patients with a history of smoking and alcohol use, metabolic disorders, or those treated with antiretrovirals or anticonvulsants.[5] Therefore, its etiology is multifactorial, associated with both intrinsic and extrinsic factors.[3]

Today, several treatment options are available, including percutaneous fasciotomy, fasciotomy using collagenase (from Clostridium histolyticum), partial or selective fasciectomy, total fasciectomy, and dermofasciectomy.[6] However, the recurrence rate of the disease is high.[7] Surgical intervention is indicated after functional impairment,[8] and it is typically recommended for patients with at least 30° of metacarpophalangeal joint contracture and/or proximal interphalangeal joint contracture associated with functional impairment.[9]

Selective fasciectomy is the most frequently performed surgical procedure for Dupuytren disease, and it is deemed the gold standard for the primary release of flexion contracture.[10] The literature is inconsistent in defining the percentage of contracture correction and recurrence rate, making it difficult to assess the effectiveness and safety of surgical interventions for Dupuytren disease.[11] In addition, an important aspect for surgical treatment evaluation is patient satisfaction after the intervention, which is not always related to a greater flexion contracture correction, hindering the comparison of therapeutic options.[12]

The present study aimed to describe the epidemiological and clinical profile of patients with Dupuytren disease surgically treated with selective fasciectomy. In addition, the present study attempted to determine the frequency of surgical complications, the need for new surgical procedures, and potential factors associated with the clinical characteristics of this condition.


#

Materials and Methods

This is a retrospective observational descriptive study of a sample of patients with Dupuytren disease who were seen and surgically treated by the Hand Surgery Service of a tertiary hospital from the Brazilian Unified Health System (SUS, in the Portuguese acronym), from January 1, 2013 to June 30, 2019. The study protocol was approved by the Institutional Research Ethics Committee (3.100.284/2018).

Selective fasciectomy was the main treatment option for Dupuytren disease during the study period, corresponding to 96.6% of the procedures performed in these patients. To homogenize the sample, patients with Dupuytren disease diagnosis confirmed by a hand surgeon were treated with an isolated primary selective fasciectomy ([Figure 1]) (n = 247). This was the first surgical approach for disease treatment, and no other procedures were performed, including capsulotomies or tenotomies. Patients previously submitted to surgical treatment and those with unavailable information in medical records were excluded.

Zoom Image
Fig. 1 Flowchart to select patients with Dupuytren disease surgically treated by primary selective fasciectomy.

Demographics were obtained through an active search in medical records, and the following information was recorded in a data collection instrument: (i) sociodemographic features, such as gender, age, self-declared skin color, weight, height, smoking and alcohol intake; (ii) positive history for diabetes mellitus, dyslipidemia, epilepsy, cardiovascular diseases, hypertension, HIV seropositivity, Ledderhose disease, Peyronie disease, adhesive shoulder capsulitis or hand trauma; and (iii) clinical presentation of Dupuytren disease: unilateral or bilateral involvement, affected rays, presence of Garrod dorsal nodules, age at onset of symptoms, positive family history for the disease, intra- and postoperative complications, length of follow-up after primary selective fasciectomy, and the need for a new surgical approach to treat a complication associated with the initial selective fasciectomy or due to recurrence of flexion contracture in the fingers, which is deemed a reintervention. Postoperative complications included an extension deficit with no report of any apparent cause, such as scar retraction, pain, or other intercurrence, in the medical record.

Surgery was indicated for functional impairment,[8] metacarpophalangeal joint flexion contracture > 30° and/or proximal interphalangeal joint contracture ([Figure 2A]). Selective fasciectomy was performed with limb exsanguination using a pneumatic cuff. The volar face of the hand was incised as popularized by Bruner, extending to the affected radius ([Figure 2B]). After mobilization of skin flaps, neurovascular bundles and the thickened palmar fascia were dissected, identified, and protected. Next, the affected fascia was excised ([Figure 2C]). This specimen ([Figure 2D]) was sent for histopathological study, confirming the characteristic changes associated with Dupuytren disease. A dressing and a volar plaster cast were applied to maintain extension of the fingers. The plastered immobilization was removed when the first dressing was changed, around the end of the 1st week. Then, passive and/or active finger mobility was initiated by the team of occupational therapists specialized in hand surgery. None of the included patients used orthosis during the postoperative period.

Zoom Image
Fig. 2 Selective fasciectomy in a patient with Dupuytren disease. (A) Flexion contracture of the little finger. (B) Surgical planning. (C) Palmar fascia thickening with chord formation. (D) Excised palmar fascia segment.

Continuous variables were presented as mean ± standard deviation (SD). Factors associated with clinical characteristics of Dupuytren disease were determined based on odds ratios (ORs) and their respective 95% confidence intervals (CIs) estimative using the multivariate logistic regression method. This univariate analysis considered both the biological importance and the degree of statistical significance; p-values ≤ 0.25 and ≤ 0.10, respectively, were required for regression model input and maintenance. The analyzes were performed using IBMSPSS Statistics for Windows, version 20.0 (IBM Corp., Armonk, NY, USA), and statistical significance was set as p < 0.05.


#

Results

The majority of the 247 patients with Dupuytren disease treated with selective fasciectomy were male, self-declared white ([Table 1]), reporting alcohol use (59.6%) and/or smoking (49.0%). Their mean age was 66.3 ± 9.2 years old (minimum, 31 and maximum, 94). Most subjects (84.4%) had a body mass index (BMI) ranging from 18.5 to 29.9 kg/m2. As for comorbidities associated with Dupuytren disease, 29.6% of the patients had diabetes mellitus, 17.3% dyslipidemia, 6.6% epilepsy, and 2.5% cardiovascular diseases; less than 1% were HIV-positive. In addition, 51.9% of the subjects reported high blood pressure.

Table 1

Variables

Dupuytren (n = 247)

n (%)

Age (years old)

 ≤ 40

2 (0.8)

 41–50

6 (2.4)

 51–60

53 (21.5)

 61–70

110 (44.5)

 71–80

62 (25.1)

 81–90

13 (5.3)

 ≥ 91

1 (0.4)

Gender

 Female

40 (16.2)

 Male

207 (83.8)

Skin color [a]

 White

161 (65.2)

 Brown

58 (23.5)

 Black

27 (10.9)

 Yellow

1 (0.4)

Bilateral hand involvement was observed in 73.3% of the patients. The little (35.0%) and ring (34.7%) fingers were the most affected rays, followed by the thumb, middle and index fingers, with 15.1, 12.1 and 3.1% of involvement, respectively. In addition, 37.2 and 38.9% of the patients had, respectively, 1 and 2 affected rays. The remaining patients had 3 (18.4%) or more affected rays (5.5%). About 11.1% of the patients also had a previous history of hand trauma, 19.7% of Ledderhose disease, 7.5% of Peyronie disease (considering the 207 affected men), 7.2% of adhesive shoulder capsulitis, and 27.8% of Garrod dorsal nodules, affecting most the index finger (33.4%), followed by the middle and ring (25.9% each) fingers, the little finger (11.1%) and the thumb (3.7%). A family history of Dupuytren disease was reported in 18.5% of the cases, and 3.7% of the patients had ≥ 3 affected relatives.

In total, 300 selective fasciectomies were performed as the first surgical approach in these 247 patients with Dupuytren disease. Patients with bilateral involvement (n = 181) underwent primary selective fasciectomy in each hand (n = 53) at different times ([Figure 1]). Considering patients with a minimum follow-up period of 1 year, the frequency of reintervention was 5.2%. The following reinterventions were performed during the study: surgical dressing due to surgical wound complication; selective fasciectomy associated with volar capsutolomy at the proximal interphalangeal joint, and z-plasty for scar contracture; selective fasciectomy associated only with volar capsulotomy of the proximal interphalangeal joint; 5th finger amputation; and isolated selective fasciectomies.

Regarding intraoperative complications of selective fasciectomies, 2 cases of digital nerve injury (0.6%) were recorded. Another case of digital nerve injury was recorded during the reintervention of a patient who underwent a new selective fasciectomy. All three cases were primarily repaired but presented some sensorial loss in the affected finger. A total of 73 complications were recorded after the 300 primary selective fasciectomies (24.3%). The most common complication was a deficit in complete extension of the affected finger (50.7%), followed by joint stiffness (24.7%) and skin necrosis (8.2%). The remaining complications totaled 16.4% ([Figure 3]).

Zoom Image
Fig. 3 Number of postoperative complications in patients with Dupuytren disease treated with selective fasciectomy.

Factors associated with the severity of Dupuytren disease were determined at a multivariate analysis. Male gender was associated with bilateral hand involvement and the number of affected rays ([Table 2]). Dyslipidemia was associated with reintervention (p = 0.04; OR = 5.7; 95%CI: 1.03–31.4). Patients with bilateral involvement had a higher number of postoperative complications (35.7 versus 19.7% in patients with unilateral involvement, OR = 2.27; 95%CI = 1.15–4.46). Other evaluated factors (age, skin color, alcohol intake, smoking, diabetes mellitus, dyslipidemia, epilepsy, HIV and surgical complications) were not significantly associated with bilateral disease, number of affected rays (1 ray versus ≥ 2 rays), age at disease onset (≤50 years old versus ≥ 51 years old) or need for reintervention.

Table 2

Variables

Unilateral (n = 66)

Bilateral (n = 181)

p-value[a]

Adjusted odds ratio (95% confidence interval)

Gender

n (%)

 Female

16 (24.2)

24 (13.3)

0.04

1[b]

 Male

50 (75.8)

157 (86.7)

2.10 (1.03–4.31)[c]

1 ray ( n  = 71)

≥ 2 rays (n = 176)

Gender

 Female

20 (28.2)

20 (11.4)

0.001

1[b]

 Male

51 (71.8)

156 (88.6)

3.41 (1.66–7.03)[d]


#

Discussion

Dupuytren disease is common in the hand surgery specialist office. However, several aspects remain inconsistent, including its etiology and the most appropriate treatment option for the clinical presentation.

Classically, Dupuytren disease mainly affects white males, > 50 years old,[5] [13] [14] and its prevalence increases with age.[13] We noted a predominance of white or brown individuals, aged > 50 years old. A 5:1 ratio between men and women was observed, which is consistent with previous descriptions (5.9:1).[13] Moreover, males were associated with an approximately two-fold higher risk for the most severe disease (bilateral involvement and more than two affected rays). Hindocha et al.[15] reported that bilateral presentation and male gender are associated with a greater recurrence of Dupuytren disease after surgical treatment.

Bilateral disease involving the little and ring fingers was commonly observed in our sample, which is consistent with the literature.[5] [6] [13] [16] Garrod dorsal nodules were more frequent in the index finger, as previously described.[17] These nodules have been associated with an increased risk of Dupuytren diathesis.[18]

Alcohol intake and smoking have been associated with Dupuytren disease.[5] [13] [19] The cause and the mechanisms of such associations remain unclear. Most patients have a history of alcohol intake and smoking; however, in a greater proportion than evidenced by Mansur et al.[5] when evaluating a smaller number of Brazilian patients (n = 58) with Dupuytren disease (9 and 22%, respectively, compared with 60 and 49% in our study). Smoking and alcohol intake are associated with the need for surgical treatment for Dupuytren disease.[13] Since our sample consisted only of patients undergoing surgical treatment, potentially with more severe presentations, the prevalence of alcoholics and smokers is higher when compared with the data described by Mansur et al.[5]

Among conditions associated with Dupuytren disease, 29.6% of the patients presented diabetes mellitus. In a series with only 58 cases of Brazilian patients with Dupuytren disease, Mansur et al.[5] found a 44.8% prevalence of diabetes, with 62% of insulin-dependent subjects. Recently, a meta-analysis observed an approximately three-fold risk association between Dupuytren disease and diabetes mellitus.[20] Although the molecular mechanism involved in both conditions has been widely studied,[20] it is suggested that the metabolites generated by diabetes mellitus stimulate the development of myofibroblasts, the main cell type involved in Dupuytren disease.[21] In addition, the majority of patients had arterial hypertension, consistent with the aforementioned study from Mansur et al.,[5] in which 55% of the subjects presented it.[5] Both conditions mainly affect elderly patients, but the cause of the association between arterial hypertension and Dupuytren disease has not been described in the literature.

The rate of reintervention after the surgical treatment for Dupuytren disease depends on several factors, including contracture severity and the type of procedure performed. The observed reintervention rate (5.2%) was consistent with a recent description in the American population, which evaluated 132 selective fasciectomies and detected a reintervention rate of 4%.[22] The multivariate analysis revealed an association between dyslipidemia and a higher rate of reintervention. Dyslipidemia has been associated with Dupuytren disease,[23] suggesting the need to consider this condition in patients with palmar fibromatosis for proper treatment planning

In a comprehensive review, Denkler[24] reported that the rate of surgical complications after primary selective fasciectomy ranged from 4 to 39%.[24] We observed a low rate of intraoperative complications, consisting only of digital nerve injury (0.6%). According to the literature, the average rate of digital nerve injury is ∼ 3%.[24] [25] The most common postoperative complications included wound healing issues, ranging from 0 to 86%.[24] However, in our sample, the most common postoperative complication was a complete extension deficit, followed by joint stiffness. In addition, patients with bilateral involvement had an approximately two-fold higher risk of postoperative complications, as the contracture may have been aggravated by the longer waiting time for surgical treatment of the contralateral hand. Ribak et al.[6] described a case of transient digital nerve paresthesia and type I regional complex pain syndrome as complications after resection of the affected fascia during a study comparing selective and percutaneous fasciectomy. In addition, they observed no significant differences between groups submitted to different fasciectomies regarding the Tubiana classification, time to resume professional activities and disease recurrence.[6]

Since this is a retrospective study, the absence of a standardized electronic medical record system and the lack of determining the degree of flexion contracture of the fingers to aid disease recurrence identification after selective fasciectomy are our main limitations. However, the sample size, as well as information confirmation through a double database check contribute to the robustness of our results, which can be used to build a database of different populations to identify disease-associated factors. Together, this information can assist in prognosis and postoperative follow-up, suggesting the need for early referral to a specialist, even with no functional limitation of the hand, which is the main determinant for the surgical treatment of Dupuytren disease.


#

Conclusion

Selective fasciectomy showed a low rate of reintervention and surgical complications. Male gender was associated with bilateral hand involvement and a higher number of affected rays, while dyslipidemia was associated with reintervention.


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Conflito de interesses:

Os autores declaram não haver conflito de interesses.

Financial Support

There was no financial support from public, commercial, or non-profit sources.


* Study developed at Instituto Nacional de Traumatologia e Ortopedia (INTO), Rio de Janeiro, RJ, Brazil.


  • Referências

  • 1 Liu H, Yin W, Liu B, Liu Y, Guo B, Wei Z. Screening of candidate genes in fibroblasts derived from patients with Dupuytren's contracture using bioinformatics analysis. Rheumatol Int 2015; 35 (08) 1343-1350
  • 2 Staats KA, Wu T, Gan BS, O'Gorman DB, Ophoff RA. Dupuytren's disease susceptibility gene, EPDR1, is involved in myofibroblast contractility. J Dermatol Sci 2016; 83 (02) 131-137
  • 3 Becker K, Siegert S, Toliat MR. et al; German Dupuytren Study Group. Meta-analysis of genome-wide association studies and network analysis-based integration with gene expression data identify new suggestive loci and unravel a Wnt-centric network associated with Dupuytren's disease. PLoS One 2016; 11 (07) e0158101
  • 4 Ji X, Tian F, Tian L. Identification and function analysis of contrary genes in Dupuytren's contracture. Mol Med Rep 2015; 12 (01) 482-488
  • 5 Mansur HG, Oliveira ER, Gonçalves CB. Epidemiological analysis of patients with Dupuytren's disease. Rev Bras Ortop 2017; 53 (01) 10-14
  • 6 Ribak S, Borkowski Jr R, do Amaral RP, Massato A, Ávila I, de Andrade D. Dupuytren contracture: comparative study between partial fasciectomy and percutaneous fasciectomy. [Contratura de Dupuytren: estudo comparativo entre fasciectomia parcial e fasciotomia percutânea]. Rev Bras Ortop 2014; 48 (06) 545-553
  • 7 Dias JJ, Braybrooke J. Dupuytren's contracture: an audit of the outcomes of surgery. J Hand Surg Br 2006; 31 (05) 514-521
  • 8 Shih B, Bayat A. Scientific understanding and clinical management of Dupuytren disease. Nat Rev Rheumatol 2010; 6 (12) 715-726
  • 9 Smith AC. Diagnosis and indications for surgical treatment. Hand Clin 1991; 7 (04) 635-642
  • 10 Desai SS, Hentz VR. The treatment of Dupuytren disease. J Hand Surg Am 2011; 36 (05) 936-942
  • 11 Werker PM, Pess GM, van Rijssen AL, Denkler K. Correction of contracture and recurrence rates of Dupuytren contracture following invasive treatment: the importance of clear definitions. J Hand Surg Am 2012; 37 (10) 2095-2105.e7
  • 12 Poelstra R, van Kooij YE, van der Oest MJW, Slijper HP, Hovius SER, Selles RW. Hand-Wrist Study Group. Patient's satisfaction beyond hand function in Dupuytren's disease: analysis of 1106 patients. J Hand Surg Eur Vol 2020; 45 (03) 280-285
  • 13 Hindocha S, McGrouther DA, Bayat A. Epidemiological evaluation of Dupuytren's disease incidence and prevalence rates in relation to etiology. Hand (N Y) 2009; 4 (03) 256-269
  • 14 Barros F, Barros A, Almeida SF. Enfermidade de Dupuytren: avaliação de 100 casos. Rev Bras Ortop 1997; 32 (03) 177-183
  • 15 Hindocha S, Stanley JK, Watson S, Bayat A. Dupuytren's diathesis revisited: Evaluation of prognostic indicators for risk of disease recurrence. J Hand Surg Am 2006; 31 (10) 1626-1634
  • 16 Dolmans GH, de Bock GH, Werker PM. Dupuytren diathesis and genetic risk. J Hand Surg Am 2012; 37 (10) 2106-2111
  • 17 Carloni R, Gandolfi S, Elbaz B, Bonmarchand A, Beccari R, Auquit-Auckbur I. Dorsal Dupuytren's disease: a systematic review of published cases and treatment options. J Hand Surg Eur Vol 2019; 44 (09) 963-971
  • 18 Hahn P. Epidemiologie des Morbus Dupuytren. Orthopade 2017; 46 (04) 298-302
  • 19 Burge P, Hoy G, Regan P, Milne R. Smoking, alcohol and the risk of Dupuytren's contracture. J Bone Joint Surg Br 1997; 79 (02) 206-210
  • 20 Broekstra DC, Groen H, Molenkamp S, Werker PMN, van den Heuvel ER. A Systematic Review and Meta-Analysis on the Strength and Consistency of the Associations between Dupuytren Disease and Diabetes Mellitus, Liver Disease, and Epilepsy. Plast Reconstr Surg 2018; 141 (03) 367e-379e
  • 21 Yuen A, Laschinger C, Talior I. et al. Methylglyoxal-modified collagen promotes myofibroblast differentiation. Matrix Biol 2010; 29 (06) 537-548
  • 22 Leafblad ND, Wagner E, Wanderman NR. et al. Outcomes and Direct Costs of Needle Aponeurotomy, Collagenase Injection, and Fasciectomy in the Treatment of Dupuytren Contracture. J Hand Surg Am 2019; 44 (11) 919-927
  • 23 Hindocha S. Risk Factors, Disease Associations, and Dupuytren Diathesis. Hand Clin 2018; 34 (03) 307-314
  • 24 Denkler K. Surgical complications associated with fasciectomy for dupuytren's disease: a 20-year review of the English literature. Eplasty 2010; 10: e15
  • 25 Dias JJ, Aziz S. Fasciectomy for Dupuytren Contracture. Hand Clin 2018; 34 (03) 351-366

Endereço para correspondência

Jamila Alessandra Perini, PhD
Instituto Nacional de Traumatologia e Ortopedia (INTO)
Divisão de Pesquisa. Av. Brasil, 500, Caju, Rio de Janeiro, RJ, 20940-070
Brasil   

Publication History

Received: 22 April 2020

Accepted: 17 September 2020

Article published online:
22 March 2021

© 2021. Sociedade Brasileira de Ortopedia e Traumatologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commecial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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  • Referências

  • 1 Liu H, Yin W, Liu B, Liu Y, Guo B, Wei Z. Screening of candidate genes in fibroblasts derived from patients with Dupuytren's contracture using bioinformatics analysis. Rheumatol Int 2015; 35 (08) 1343-1350
  • 2 Staats KA, Wu T, Gan BS, O'Gorman DB, Ophoff RA. Dupuytren's disease susceptibility gene, EPDR1, is involved in myofibroblast contractility. J Dermatol Sci 2016; 83 (02) 131-137
  • 3 Becker K, Siegert S, Toliat MR. et al; German Dupuytren Study Group. Meta-analysis of genome-wide association studies and network analysis-based integration with gene expression data identify new suggestive loci and unravel a Wnt-centric network associated with Dupuytren's disease. PLoS One 2016; 11 (07) e0158101
  • 4 Ji X, Tian F, Tian L. Identification and function analysis of contrary genes in Dupuytren's contracture. Mol Med Rep 2015; 12 (01) 482-488
  • 5 Mansur HG, Oliveira ER, Gonçalves CB. Epidemiological analysis of patients with Dupuytren's disease. Rev Bras Ortop 2017; 53 (01) 10-14
  • 6 Ribak S, Borkowski Jr R, do Amaral RP, Massato A, Ávila I, de Andrade D. Dupuytren contracture: comparative study between partial fasciectomy and percutaneous fasciectomy. [Contratura de Dupuytren: estudo comparativo entre fasciectomia parcial e fasciotomia percutânea]. Rev Bras Ortop 2014; 48 (06) 545-553
  • 7 Dias JJ, Braybrooke J. Dupuytren's contracture: an audit of the outcomes of surgery. J Hand Surg Br 2006; 31 (05) 514-521
  • 8 Shih B, Bayat A. Scientific understanding and clinical management of Dupuytren disease. Nat Rev Rheumatol 2010; 6 (12) 715-726
  • 9 Smith AC. Diagnosis and indications for surgical treatment. Hand Clin 1991; 7 (04) 635-642
  • 10 Desai SS, Hentz VR. The treatment of Dupuytren disease. J Hand Surg Am 2011; 36 (05) 936-942
  • 11 Werker PM, Pess GM, van Rijssen AL, Denkler K. Correction of contracture and recurrence rates of Dupuytren contracture following invasive treatment: the importance of clear definitions. J Hand Surg Am 2012; 37 (10) 2095-2105.e7
  • 12 Poelstra R, van Kooij YE, van der Oest MJW, Slijper HP, Hovius SER, Selles RW. Hand-Wrist Study Group. Patient's satisfaction beyond hand function in Dupuytren's disease: analysis of 1106 patients. J Hand Surg Eur Vol 2020; 45 (03) 280-285
  • 13 Hindocha S, McGrouther DA, Bayat A. Epidemiological evaluation of Dupuytren's disease incidence and prevalence rates in relation to etiology. Hand (N Y) 2009; 4 (03) 256-269
  • 14 Barros F, Barros A, Almeida SF. Enfermidade de Dupuytren: avaliação de 100 casos. Rev Bras Ortop 1997; 32 (03) 177-183
  • 15 Hindocha S, Stanley JK, Watson S, Bayat A. Dupuytren's diathesis revisited: Evaluation of prognostic indicators for risk of disease recurrence. J Hand Surg Am 2006; 31 (10) 1626-1634
  • 16 Dolmans GH, de Bock GH, Werker PM. Dupuytren diathesis and genetic risk. J Hand Surg Am 2012; 37 (10) 2106-2111
  • 17 Carloni R, Gandolfi S, Elbaz B, Bonmarchand A, Beccari R, Auquit-Auckbur I. Dorsal Dupuytren's disease: a systematic review of published cases and treatment options. J Hand Surg Eur Vol 2019; 44 (09) 963-971
  • 18 Hahn P. Epidemiologie des Morbus Dupuytren. Orthopade 2017; 46 (04) 298-302
  • 19 Burge P, Hoy G, Regan P, Milne R. Smoking, alcohol and the risk of Dupuytren's contracture. J Bone Joint Surg Br 1997; 79 (02) 206-210
  • 20 Broekstra DC, Groen H, Molenkamp S, Werker PMN, van den Heuvel ER. A Systematic Review and Meta-Analysis on the Strength and Consistency of the Associations between Dupuytren Disease and Diabetes Mellitus, Liver Disease, and Epilepsy. Plast Reconstr Surg 2018; 141 (03) 367e-379e
  • 21 Yuen A, Laschinger C, Talior I. et al. Methylglyoxal-modified collagen promotes myofibroblast differentiation. Matrix Biol 2010; 29 (06) 537-548
  • 22 Leafblad ND, Wagner E, Wanderman NR. et al. Outcomes and Direct Costs of Needle Aponeurotomy, Collagenase Injection, and Fasciectomy in the Treatment of Dupuytren Contracture. J Hand Surg Am 2019; 44 (11) 919-927
  • 23 Hindocha S. Risk Factors, Disease Associations, and Dupuytren Diathesis. Hand Clin 2018; 34 (03) 307-314
  • 24 Denkler K. Surgical complications associated with fasciectomy for dupuytren's disease: a 20-year review of the English literature. Eplasty 2010; 10: e15
  • 25 Dias JJ, Aziz S. Fasciectomy for Dupuytren Contracture. Hand Clin 2018; 34 (03) 351-366

Zoom Image
Fig. 1 Fluxograma para seleção dos pacientes com diagnóstico de doença de Dupuytren tratados cirurgicamente por fasciectomia seletiva primária.
Zoom Image
Fig. 2 Fasciectomia seletiva em paciente com doença de Dupuytren. (A) Contratura em flexão do dedo mínimo. (B) Planejamento operatório. (C) Espessamento da fáscia palmar com formação de corda. (D) Segmento da fáscia palmar excisada.
Zoom Image
Fig. 1 Flowchart to select patients with Dupuytren disease surgically treated by primary selective fasciectomy.
Zoom Image
Fig. 2 Selective fasciectomy in a patient with Dupuytren disease. (A) Flexion contracture of the little finger. (B) Surgical planning. (C) Palmar fascia thickening with chord formation. (D) Excised palmar fascia segment.
Zoom Image
Fig. 3 Número de complicações pós-operatórias dos pacientes com doença de Dupuytren tratados com fasciectomia seletiva.
Zoom Image
Fig. 3 Number of postoperative complications in patients with Dupuytren disease treated with selective fasciectomy.