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Title: Efficacy of Injectable Collagenase in the treatment of Dupuytren’s contracture
in comparison to Partial Fasciectomy
Authors: Mohamed A. El Rouby, MD, Ahmed Abd El Salam, MD, Ahmed Gad, MD Khaled
Rizq, MD
Plastic and Reconstructive Surgery Department, Ain Shams University, Cairo, EGYPT.
Accepted: Egyptian Journal of Plastic and Reconstructive Surgery
Abstract:
Background: Dupuytren's disease as a benign fibroproliferative disease with an abnormal
slowly progressive thickening and shorting of the palmar aponeurosis leads to severe
functional limitations in the finger movements particularly of the metacarpophalangeal
(MCP) joints and/or the proximal interphalangeal (PIP) joints. The authors aimed to
evaluate the role of injectable collagenase (CCH) in the treatment of Dupuytren’s
contracture in comparison to surgical treatment.
Material and method: This study included 15 patients (33 rays), They were divided into
two groups, Group A: 26 rays underwent open fasciectomy. (10 patients) and Group B: 7
rays were treated by collagenase injection. (5 patients). Exclusion criteria for group B
were contraindications of injection of CCH. The primary efficacy variable was clinical
success, contracture correction to within 5° of normal (normal = 0°) by using goniometry.
Additional efficacy variables included the time and number of injections required to
achieve success in the primary joint. Recurrence rate and adverse effects were recorded.
Results: Initial clinical experience was recorded of 5 patients (7rays) (mean age 57 years)
and compared to previously surgically managed 10 patients (26 rays) (mean age 59
years). Of all population, 51% for little, 47% for ring, 1% for middle and 1% for index
fingers. The mean of the pre-intervention fixed flexion contracture in the MCP joint was
39° and improved to one-year postintervention 14°, and in the PIP joint 47° to 19°. In
group B one ray with no improvement at all and recurrence in one ray. Partial stretching
was achieved in one ray. No serious complications were observed after injections. In
cases of group A (26 rays) that was treated by partial fasciectomy, recurrence occurred
in 6 rays and nerve injuries as nerve division and neuropraxia occurred in 2 rays.
Conclusion: The treatment of Dupuytren's disease with injectable collagenase is safe and
effective. However, the financial aspects should be considered especially in developing
countries.
keywords
Dupuytren finger collagenase Fasciectomy
Introduction
Dupuytren's disease (MD) is a benign fibroproliferative disorder, named after Baron
Guillaume Dupuytren’s (1777-1835) (1, 2), with an abnormal slowly progressive
thickening and shorting of the palmar aponeurosis. The etiology of this disease remains
unclear, so far, no cure is possible. It particularly affects the metacarpophalangeal (MCP)
joints and/or the proximal interphalangeal (PIP) joints. It usually affects the ring and little
fingers. (2)
The management of the Dupuytren's disease can be done with different modalities. The
aim of all previously described therapeutic procedures is to restore normal hand function.
Although surgical procedures (partial fasciectomy and fasciotomy) are still the standard,
the collagenase Clostridium histolyticum (CCH) has been approved as safe and effective
treatment option for several years. This enzymatic substance can cleave peptide bonds
and degrade collagens (all human collagen types). It has the advantages of the treatment
of older patients with co-morbidities, an earlier return to work, eliminate the risks of
surgery(3-11).
However, it should also be noted that the results of collagenase treatment of isolated
MCP contractures are significantly better than isolated PIP contractures or combined
MCP / PIP contractures. Also, repeated injections of collagenase appear to be safe and
effective despite the patient's antibody production because of repeated exposure. In a
case report from a patient who received 15 injections over 4 years, it was found that the
effect was still good in the MCP joint but slightly decreased in the PIP (12-15).
In Egypt, the commercially available collagenases (Xiapex®, 0.9 mg vial, Swedish
Orphan Biovitrum Ltd., Sweden or Xiaflex 0.9 mg vial, Endo International plc) are a
mixture, which is comprised mostly of interstitial collagen types I and III (16, 17).
The most common complications of this non-surgical technique are swelling, effusion,
hematoma or pain. Most of these adverse effects are mild or moderate and self-limiting
within an average of 10 days. Regarding the financial aspects of collagenase treatment,
another disadvantage of this procedure is the higher cost that could be 200 up to 400
USD per vial (18-20).
In a review by Chen et al. in 2011, compared the recurrence rates of surgical versus Non-
surgical procedures showed. It was significantly higher in needle aponeurotomy than in
open partial fasciectomy, and in open partial fasciectomy also appeared to be significantly
higher than in CCH injection (18).
In 2013, the safety and efficacy of CCH injections were explored again in two studies. A
total of 879 joints in 587 patients at 34 institutions were treated in the study. The treatment
at an early stage is more beneficial. In 57% of the patients treatment was successful (0-
5 ° extension within 30 days), with more improvement in MCP than PIP joints (70 vs.
37%)(5). The recurrence rate was comparable to standard surgical procedures. (21)
For the treatment of Dupuytren's related disease as Peyronie's disease, the use of CCH
is both effective and safe by injection of CCH directly into the tunica albuginea (22).
In this study, we aimed to evaluate the efficacy of injectable collagenase (Xiapex®, 0.9
mg vial, Pfizer Limited, Kent, UK) in the treatment of Dupuytren’s contracture in
comparison to traditional partial fasciectomy.
Material and Methods
This study included 15 patients (33 rays), (4 patients with 1 ray, 6 patients with 2 rays 3
patients with 3 rays, 2 patients with 2 rays) with flexion deformities of the MCP and/or PIP
joints of 20° or greater. Their age ranged from 40 to 65 years. They were divided into two
groups:
Group A: 26 rays underwent open fasciectomy. (10 patients)
Group B: 7 rays were treated by collagenase injection. (5 patients)
Exclusion criteria for group B were contraindications of injection of CCH as pregnancy,
hypersensitivity to collagenase or patients uses anticoagulant.
All the patients’ results were recorded at 3rd, 6th and 18th moths. The primary efficacy
variable was clinical success, contracture correction to within 5° of normal (normal = 0°)
by using goniometry. Additional efficacy variables included the time and number of
injections required to achieve success in the primary joint. Recurrence rate and adverse
effects were recorded. Common side effects include local swelling, redness, or pain at
the site of puncture was also recorded.
Injection Procedure:
After injection of local anesthetic (Lidocaine 1:200000), 0.3 mg per injection of Xiapex®
(0.9 mg vial, Pfizer Limited, Kent, UK) (23) was injected into the palpable cord. After 24 –
72 hours, we perform finger extension procedure to facilitate cord disruption for
approximately 10-20 seconds. If the first attempt to extend the finger is unsuccessful, a
second and a third attempt can be made at intervals of 5-10 minutes each without
increasing the force. The patients were instructed to use splint for 10 days with active and
passive extension exercises. Injection was repeated after Four weeks, if the MCP or PIP
contracture remains, up to a maximum of 3 injections in the same strand.
Results
Initial clinical experience was recorded of 5 patients (7rays) (4 males, 1 female, mean
age 57 [range 40-61] years) (Fig.1,2) and compared to previously surgically managed 10
patients (26 rays) (7 males, 3 females mean age 59 [range 42 – 65] years) (Fig. 3,4)
.(Table 1) Of all population, 51% were treated for little fingers, 47% for ring fingers, 1%
for middle fingers and 1% for index fingers.
Figure 1: Pre and 6 months
after injection (Group B)
Figure 2: Lateral view show
improvement of flexion
deformity of left PIP joint of ring
finger from 35° to 15°.
Figure 3: Preoperative and intraoperative of partial fasciectomy (Group A)
Table 1: number of treated rays in each group:
Group A: 26 rays underwent open fasciectomy. (10 patients)
(1 patient →1 ray 4 patients →2 rays 3 patients →3 rays 2 patients →2 rays)
Group B: 7 rays were treated by collagenase injection. (5 patients)
(3 patients →1 ray 2 patient →2 rays)
A successful strand solution was defined as achieving 0-5 ° extension of the affected joint.
This was achieved in all group B cases except one ray with no improvement at all and
recurrence in one ray. Partial stretching was achieved in one ray.
The mean of the pre-intervention fixed flexion contracture in the MCP joint was 39° and
improved to one-year postintervention 14°, and in the PIP joint 47° to 19°. (Fig 2)
No serious complications (tendon / ligament ruptures, nerve lesions or hypersensitivity
reactions) were observed after injections. In cases of group A (26 rays) that was treated
by partial fasciectomy, recurrence occurred in 6 rays and nerve injuries as nerve division
and neuropraxia occurred in 2 rays. (Table 2)
Figure 4: Lateral view show
improvement of flexion
deformity of left MCP joint of
little finger from 49° to 9°.
Table 2: Recorded Complication in both groups:
Open Fasciectomy (26 rays) Collagenase injection (7 rays)
Recurrence 6/26
Nerve division 1/26
Neuropraxia 1/26
Infection 0
Skin sloughing 0
Recurrence 1/7
Failure of treatment 1/7
Partial Stretch 1/7
Nerve injury 0
Hypersensitivity 0
Discussion
Our experience has shown that the use of injectable collagenase is an effective and well-
tolerated alternative to surgical treatment.
The patient must, however, be informed about the frequent occurrence of undesired side
effects (especially cost and hypersensitivity) as well as recurrence rate and
ineffectiveness of the treatment that may need surgical intervention.
As regard the undesirable side effects in group B, they were minimally and self-limiting
like swelling, bleeding, pain, redness in the puncture site. No nerve lesions were detected.
In elderly patients with multiple co-morbidities, who should avoid anesthesia or
postoperative wound healing problems, treatment with CCH is a very good alternative.
The effectiveness and patient satisfaction of collagenase treatment versus partial
fasciectomy are comparable; In view of the earlier return to work and surgical
complications, collagenase injection has the advantage.
However, the question of the significance in relation to partial fasciectomy cannot yet be
answered conclusively. The published recurrence rate shows considerable differences.
The method will have to be measured for the long-term recurrence rate and
complications.
Conclusion
The treatment of Dupuytren's disease with injectable collagenase has been proven safe
and effective, as confirmed by recent studies. However, the financial aspects should be
considered especially in developing countries.
Conflict of interest
There is no conflict of interest.
References
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diagnosis, and treatment. J Plastic reconstructive surgery 2007;120:44e-54e.
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opinion on biological therapy 2010;10:1395-1404.
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Dupuytren’s contracture: results from POINT X, an open-label study of clinical and patient-reported
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Efficacy of Injectable Collagenase in the treatment of Dupuytren’s contracture in comparison to Partial Fasciectomy

  • 1. Title: Efficacy of Injectable Collagenase in the treatment of Dupuytren’s contracture in comparison to Partial Fasciectomy Authors: Mohamed A. El Rouby, MD, Ahmed Abd El Salam, MD, Ahmed Gad, MD Khaled Rizq, MD Plastic and Reconstructive Surgery Department, Ain Shams University, Cairo, EGYPT. Accepted: Egyptian Journal of Plastic and Reconstructive Surgery Abstract: Background: Dupuytren's disease as a benign fibroproliferative disease with an abnormal slowly progressive thickening and shorting of the palmar aponeurosis leads to severe functional limitations in the finger movements particularly of the metacarpophalangeal (MCP) joints and/or the proximal interphalangeal (PIP) joints. The authors aimed to evaluate the role of injectable collagenase (CCH) in the treatment of Dupuytren’s contracture in comparison to surgical treatment. Material and method: This study included 15 patients (33 rays), They were divided into two groups, Group A: 26 rays underwent open fasciectomy. (10 patients) and Group B: 7 rays were treated by collagenase injection. (5 patients). Exclusion criteria for group B were contraindications of injection of CCH. The primary efficacy variable was clinical success, contracture correction to within 5° of normal (normal = 0°) by using goniometry. Additional efficacy variables included the time and number of injections required to achieve success in the primary joint. Recurrence rate and adverse effects were recorded. Results: Initial clinical experience was recorded of 5 patients (7rays) (mean age 57 years) and compared to previously surgically managed 10 patients (26 rays) (mean age 59 years). Of all population, 51% for little, 47% for ring, 1% for middle and 1% for index fingers. The mean of the pre-intervention fixed flexion contracture in the MCP joint was 39° and improved to one-year postintervention 14°, and in the PIP joint 47° to 19°. In group B one ray with no improvement at all and recurrence in one ray. Partial stretching was achieved in one ray. No serious complications were observed after injections. In cases of group A (26 rays) that was treated by partial fasciectomy, recurrence occurred in 6 rays and nerve injuries as nerve division and neuropraxia occurred in 2 rays. Conclusion: The treatment of Dupuytren's disease with injectable collagenase is safe and effective. However, the financial aspects should be considered especially in developing countries. keywords Dupuytren finger collagenase Fasciectomy
  • 2. Introduction Dupuytren's disease (MD) is a benign fibroproliferative disorder, named after Baron Guillaume Dupuytren’s (1777-1835) (1, 2), with an abnormal slowly progressive thickening and shorting of the palmar aponeurosis. The etiology of this disease remains unclear, so far, no cure is possible. It particularly affects the metacarpophalangeal (MCP) joints and/or the proximal interphalangeal (PIP) joints. It usually affects the ring and little fingers. (2) The management of the Dupuytren's disease can be done with different modalities. The aim of all previously described therapeutic procedures is to restore normal hand function. Although surgical procedures (partial fasciectomy and fasciotomy) are still the standard, the collagenase Clostridium histolyticum (CCH) has been approved as safe and effective treatment option for several years. This enzymatic substance can cleave peptide bonds and degrade collagens (all human collagen types). It has the advantages of the treatment of older patients with co-morbidities, an earlier return to work, eliminate the risks of surgery(3-11). However, it should also be noted that the results of collagenase treatment of isolated MCP contractures are significantly better than isolated PIP contractures or combined MCP / PIP contractures. Also, repeated injections of collagenase appear to be safe and effective despite the patient's antibody production because of repeated exposure. In a case report from a patient who received 15 injections over 4 years, it was found that the effect was still good in the MCP joint but slightly decreased in the PIP (12-15). In Egypt, the commercially available collagenases (Xiapex®, 0.9 mg vial, Swedish Orphan Biovitrum Ltd., Sweden or Xiaflex 0.9 mg vial, Endo International plc) are a mixture, which is comprised mostly of interstitial collagen types I and III (16, 17). The most common complications of this non-surgical technique are swelling, effusion, hematoma or pain. Most of these adverse effects are mild or moderate and self-limiting within an average of 10 days. Regarding the financial aspects of collagenase treatment, another disadvantage of this procedure is the higher cost that could be 200 up to 400 USD per vial (18-20). In a review by Chen et al. in 2011, compared the recurrence rates of surgical versus Non- surgical procedures showed. It was significantly higher in needle aponeurotomy than in open partial fasciectomy, and in open partial fasciectomy also appeared to be significantly higher than in CCH injection (18). In 2013, the safety and efficacy of CCH injections were explored again in two studies. A total of 879 joints in 587 patients at 34 institutions were treated in the study. The treatment at an early stage is more beneficial. In 57% of the patients treatment was successful (0- 5 ° extension within 30 days), with more improvement in MCP than PIP joints (70 vs. 37%)(5). The recurrence rate was comparable to standard surgical procedures. (21)
  • 3. For the treatment of Dupuytren's related disease as Peyronie's disease, the use of CCH is both effective and safe by injection of CCH directly into the tunica albuginea (22). In this study, we aimed to evaluate the efficacy of injectable collagenase (Xiapex®, 0.9 mg vial, Pfizer Limited, Kent, UK) in the treatment of Dupuytren’s contracture in comparison to traditional partial fasciectomy. Material and Methods This study included 15 patients (33 rays), (4 patients with 1 ray, 6 patients with 2 rays 3 patients with 3 rays, 2 patients with 2 rays) with flexion deformities of the MCP and/or PIP joints of 20° or greater. Their age ranged from 40 to 65 years. They were divided into two groups: Group A: 26 rays underwent open fasciectomy. (10 patients) Group B: 7 rays were treated by collagenase injection. (5 patients) Exclusion criteria for group B were contraindications of injection of CCH as pregnancy, hypersensitivity to collagenase or patients uses anticoagulant. All the patients’ results were recorded at 3rd, 6th and 18th moths. The primary efficacy variable was clinical success, contracture correction to within 5° of normal (normal = 0°) by using goniometry. Additional efficacy variables included the time and number of injections required to achieve success in the primary joint. Recurrence rate and adverse effects were recorded. Common side effects include local swelling, redness, or pain at the site of puncture was also recorded. Injection Procedure: After injection of local anesthetic (Lidocaine 1:200000), 0.3 mg per injection of Xiapex® (0.9 mg vial, Pfizer Limited, Kent, UK) (23) was injected into the palpable cord. After 24 – 72 hours, we perform finger extension procedure to facilitate cord disruption for approximately 10-20 seconds. If the first attempt to extend the finger is unsuccessful, a second and a third attempt can be made at intervals of 5-10 minutes each without increasing the force. The patients were instructed to use splint for 10 days with active and passive extension exercises. Injection was repeated after Four weeks, if the MCP or PIP contracture remains, up to a maximum of 3 injections in the same strand.
  • 4. Results Initial clinical experience was recorded of 5 patients (7rays) (4 males, 1 female, mean age 57 [range 40-61] years) (Fig.1,2) and compared to previously surgically managed 10 patients (26 rays) (7 males, 3 females mean age 59 [range 42 – 65] years) (Fig. 3,4) .(Table 1) Of all population, 51% were treated for little fingers, 47% for ring fingers, 1% for middle fingers and 1% for index fingers. Figure 1: Pre and 6 months after injection (Group B) Figure 2: Lateral view show improvement of flexion deformity of left PIP joint of ring finger from 35° to 15°. Figure 3: Preoperative and intraoperative of partial fasciectomy (Group A)
  • 5. Table 1: number of treated rays in each group: Group A: 26 rays underwent open fasciectomy. (10 patients) (1 patient →1 ray 4 patients →2 rays 3 patients →3 rays 2 patients →2 rays) Group B: 7 rays were treated by collagenase injection. (5 patients) (3 patients →1 ray 2 patient →2 rays) A successful strand solution was defined as achieving 0-5 ° extension of the affected joint. This was achieved in all group B cases except one ray with no improvement at all and recurrence in one ray. Partial stretching was achieved in one ray. The mean of the pre-intervention fixed flexion contracture in the MCP joint was 39° and improved to one-year postintervention 14°, and in the PIP joint 47° to 19°. (Fig 2) No serious complications (tendon / ligament ruptures, nerve lesions or hypersensitivity reactions) were observed after injections. In cases of group A (26 rays) that was treated by partial fasciectomy, recurrence occurred in 6 rays and nerve injuries as nerve division and neuropraxia occurred in 2 rays. (Table 2) Figure 4: Lateral view show improvement of flexion deformity of left MCP joint of little finger from 49° to 9°.
  • 6. Table 2: Recorded Complication in both groups: Open Fasciectomy (26 rays) Collagenase injection (7 rays) Recurrence 6/26 Nerve division 1/26 Neuropraxia 1/26 Infection 0 Skin sloughing 0 Recurrence 1/7 Failure of treatment 1/7 Partial Stretch 1/7 Nerve injury 0 Hypersensitivity 0 Discussion Our experience has shown that the use of injectable collagenase is an effective and well- tolerated alternative to surgical treatment. The patient must, however, be informed about the frequent occurrence of undesired side effects (especially cost and hypersensitivity) as well as recurrence rate and ineffectiveness of the treatment that may need surgical intervention. As regard the undesirable side effects in group B, they were minimally and self-limiting like swelling, bleeding, pain, redness in the puncture site. No nerve lesions were detected. In elderly patients with multiple co-morbidities, who should avoid anesthesia or postoperative wound healing problems, treatment with CCH is a very good alternative. The effectiveness and patient satisfaction of collagenase treatment versus partial fasciectomy are comparable; In view of the earlier return to work and surgical complications, collagenase injection has the advantage. However, the question of the significance in relation to partial fasciectomy cannot yet be answered conclusively. The published recurrence rate shows considerable differences. The method will have to be measured for the long-term recurrence rate and complications. Conclusion The treatment of Dupuytren's disease with injectable collagenase has been proven safe and effective, as confirmed by recent studies. However, the financial aspects should be considered especially in developing countries. Conflict of interest There is no conflict of interest. References
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