Repair of Fingertip Degloving Injuries using the Extended Reverse Second Dorsal Metacarpal Artery Flap

Author:

Zhang Wenlong1,Zhang Xu2,Liu Yingnan3,Xu Tao3,Zhuang Yongqing3,Chen Chao3

Affiliation:

1. Hand and Foot Surgery, Tianjin Union Medical Center, Tianjin, 300121, China.

2. Hand Surgery Department, Third Hospital of Hebei Medical University, Shijiazhuang, Hebei, 050000, China.

3. Division of Hand, foot and microvascular surgery, Department of Orthopedics, Shenzhen People's Hospital, Second Clinical Medicine College of Jinan University, First Affiliated Hospital of Southern University of Science and Technology, Shenzhen, Guangdong, 518020, China.

Abstract

Background: This study aimed to introduce modified reverse second dorsal metacarpal artery flap (MRSDMAF) transfer for the treatment of fingertip degloving injuries. Methods: From January 2004 to March 2020, 31 patients with fingertip degloving injuries underwent MRSDMAF transfer. The mean defect and flap size were 4.5 cm×1.6 cm and 4.7 cm×1.7 cm, respectively. Nerve repair was performed in 18 fingers. Flap sensation, function restoration of the reconstructed fingers, and donor site morbidity were assessed. For comparison, we reviewed a cohort of 45 patients undergoing modified cross-finger flap (MCFF) transfer. Results: Complete flap survival was achieved in 28 fingers, and partial distal flap necrosis was noted in 3 fingers. After a mean of 24 months, the static 2PD was 8.6 ± 1.0 mm and 7.2 ± 0.8 mm in the MRSDMAF and MCFF with a significant difference (P<.0001). Sensory restoration of the MRSDMAF group was inferior to that of the MCFF group. In addition, the MRSDMAF group presented a higher incidence of fingertip pain (P = .019) and suboptimal cosmetic appearance of the reconstructed finger (P = .036). On the donor site, the MRSDMAF group presented a lower incidence of scar pain (P = .030) and better appearance (P = .025). Conclusions: MRSDMAF transfer is an alternative treatment for fingertip degloving injuries, especially when MCFF transfer is not feasible. ClinicalTrials.gov ID: NCT01019811 CLINICAL QUESTION/LEVEL OF EVIDENCE: Therapeutic IIIa.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Surgery

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