Skip to main content

Repair of distal finger soft-tissue defects with free fibular great toe neurovascular flaps

Abstract

Background

This work aimed to investigate the change in fingerprint depth and the recovery rule of fingerprint biological recognition function after repairing finger abdominal defects and rebuilding fingerprint with a free flap.

Method

From April 2018 to March 2023, we collected a total of 43 cases of repairing finger pulp defects using the free flap of the fibular side of the great toe with the digital nerve. After surgery, irregular follow-up visits were conducted to observe fingerprint clarity, perform the ninhydrin test or detect visible sweating with the naked eye. We recorded fingerprint clarity, nail shape, two-point discrimination, cold perception, warm perception and fingerprint recognition using smartphones. The reconstruction process of the repaired finger was recorded to understand the changes in various observation indicators and their relationship with the depth of the fingerprint. The correlation between fingerprint depth and neural repair was determined, and the process of fingerprint biological recognition function repair was elucidated.

Result

All flaps survived, and we observed various manifestations in different stages of nerve recovery. The reconstructed fingerprint had a clear fuzzy process, and the depth changes of the fingerprint were consistent with the changes in the biological recognition function curve.

Conclusion

The free flap with the digital nerve is used to repair finger pulp defects. The reconstructed fingerprint has a biological recognition function, and the depth of the fingerprint is correlated with the process of nerve repair. The fingerprint morphology has a dynamic recovery process, and it can reach a stable state after 6–8 months.

Peer Review reports

Introduction

Fingers are vital parts for performing the functions of what the hand normally does. As the popularity of fingerprinting equipment is increasing, fingerprint use for personal identification has become integrated in numerous scenarios, such as access to an individual’s telephone. Unfortunately, distal finger soft-tissue defects may result in much inconvenience [1]. Multiple surgical strategies (e.g. Matriderm dermal substitute, interdigital artery flaps, second-layer palmar graft and toe flaps) have been introduced for repair purposes, but the common treatments remain controversial, and the repair of defects remains challenging [2,3,4].

The skins over the fibular side of the great toe and the distal finger possess similar characteristics; both are hairless, thick and have a high density of nerve endings and eccrine sweat glands [5, 6]. Several studies have shown that this surgical strategy has advantages in terms of minor donor site morbidity, ideal form and nerve recovery [7,8,9]. However, few studies reported postoperative fingerprint recognition, and studies focusing on recovery at different times are scarce. This study aimed to fill the research gap. A total of 43 patients who underwent transplantation of neurovascular flaps from the free fibular region to the great toe because of distal finger soft-tissue defects in our medical institutions were identified. Patients were divided into six groups by intervals between the operation date and the test date. The postoperative fingerprint register and recognition were the leading targets. We also noted four other parameters: warm sense, cold sense, static two-point discrimination and ninhydrin staining.

Materials and methods

This study was guided by the Declaration of Helsinki. The Medical Ethics Committee of Guzhen People’s Hospital approved this study (Approval ID: GZLLPS 20180109-01). The candidates provided written informed consent. Tests were performed by two surgeons. When the two came to the same result, this was recorded. Once divergence occurred, another surgeon was asked for feedback. Before the tests, surgeons communicated with candidates to build trust, explain the test process and teach candidates to discriminate stimulation. The following points were noted during testing: (1) Tests should be carried out in a quiet, peaceful and comfortable environment; (2) Before testing, surgeons and candidates should wash and dry their hands. (3) We repeated all tests three times. When the three results were the same, they were recorded. Once divergence occurred, the result that appeared twice was recorded. (4) One test could last 3 s. The interval between the two tests was at least 5 s.

Inclusion and exclusion criteria

Inclusion criteria were as follows: (1) patients were younger than 60 years old; (2) crush injury to the distal fingers; and (3) patients were repaired with a free flap of the fibular side of the toe with nerve anastomosis. The blood supply vessel was the fibular side artery of the toe base. During the surgery, attention should be paid to reconstructing the fingerprint.

Exclusion criteria were as follows: (1) patients suffered from chronic diseases that affect nerve growth, like diabetes; and (2) patients had phalanx fractures or bones missing.

Grouping

The growth rate of axons during nerve regeneration varies depending on the nature of the nerve and injury. About 8 days after nerve injury, the regenerated axons begin to slowly form myelin sheaths from near to far, with a slow increase in thickness that takes about a year to complete [10, 11]. Therefore, the evaluation time for peripheral nerve regeneration should be based on different experimental purposes, nerves and injury types. If the maturity and functional recovery level of regenerated nerve fibres is evaluated, a long observation endpoint is generally selected, ranging from 3 months to more than 1 year. In general, observation is conducted at intervals of 1 month in the early postoperative period, followed by intervals of 3–6 months in the middle and late stages [12,13,14]. In this study, 43 patients were separated into six groups according to intervals between the operation date and the survey date: the 0–35 days group, the 36–75 days group, the 76–105 days group, the 106–215 days group, the 215–365 days group and the over 365 days group.

Surgical procedure and postoperative care

The same surgical team carried out all operations. The structural separation and anastomoses were performed under the microscope. The surgical procedure utilised in this study was designed based on our extensive experience and previous surgical outcomes, which were published in several Chinese medical journals. These prior studies have provided us with insights into flap reconstruction techniques, which have been instrumental in refining the current surgical approach.

According to the condition of defects, the patterns of flaps were designed at the fibular aspect of the ipsilateral or contralateral great toes by the same experienced surgeon. Compared with the diameter of defects, that of the flap was 2–3 mm larger. The expected incision did not extend beyond the centre line of the plantar. A stripe of leather was devised to prevent over-tightened suture on the pedicle.

Brachial plexus block anaesthesia was performed. A tourniquet was tied around the proximal upper arm that was badly injured. Debridement was carried out. The proper palmar digital arteries and nerves were identified. One or two veins with wide diameters were marked. We measured distances between structures.

A tourniquet was tied around the proximal thigh. Combined spinal and epidural anaesthesia was carried out. We made incisions at the proximal acrotarsium, moving to the sides; one or two veins connecting to flaps were found and intercepted. We made incisions at the web areas, moving to the sole, and the proper digital arteries and nerves were detected. The flap was peeled completely. Thin soft tissue was left to cover the surface of the phalanx. We ensured arteries and nerves were kept intact in flaps. The excess fat was removed.

We analysed the corresponding structures between defects and flaps. We made sure that the toeprints were aligned with the fingerprints.

After surgery, patients were treated with antibiotics, anticoagulants, antispasmodics and drugs to promote nerve growth activity. Visible light illumination was applied to keep it warm. Under the guidance of surgeons, rehabilitation began within 7 days. Stitches were removed at 13–14 days after surgery.

Fingerprint registers and recognition

The results of the fingerprint register and recognition were achieved by one phone. If the candidates had registered repaired fingerprints in the database and had used their repaired fingers to unlock the phone within five attempts, the result would have been marked as (1) If not, the result would have been marked as 0. Red printing oil was used to record fingerprint shapes. We set clarity ambiguity or missing record as 0, relatively clear as 1 and very clear as (2) The definition of relevant standards was as follows:

Relatively Clear: This descriptor is used when the fingerprint pattern is distinct, but certain ridge details may be slightly blurred or less distinct The overall pattern allows for a general identification, yet it may not meet the highest standards of claim required for some forms of biological analysis.

Very Clear: This term describes a fingerprint that exhibits a high degree of clarity and detail. The ridges and galleries are sharply defined, and the majority of the fingerprint’s unique characteristics can be easily identified. A very clear fingerprint would be suitable for high-precision biomedical applications and would present minimal complexity in recognition tasks.

To objectify our assessment, we implemented a standardised scoring system where the surgeons independently evaluated the claim of the fingerprints and compared their findings. In cases with disagreement, a third surgeon was consulted to reach a consensus.

Temperature sensations

We placed a metal rod into a 4 °C fluid-filled beaker. After 10 min, the metal rod was used to test cold sense. Similarly, we placed another metal rod into a 45 °C fluid-filled beaker. After 10 min, this metal rod was used to test warm sense. When we tested the temperature sensation, one end of the metal rod was directly in contact with the skin. The test was scored by blindfolded candidates themselves. If the candidate had the specified feeling, the result would have been marked as 1. If the candidate had no feelings, the result would have been marked as 0.

Function of autonomic nerves

The ninhydrin-stained sheets were copied and masked to assess the hidrotic effect [15]. Candidates drank hot water to help sweat. Their fingertips were pressed on the prepared paper. The contour of fingers was portrayed in pencil. A ninhydrin spray was used. The fingertips pressed against paper (quality copy paper) leave a print that can be dyed and fixed with a solution of 1% ninhydrin dissolved in acetone. Sweat spots would show after 24 h. We evaluated and recorded the results. If the sweat had been dyed, the result would have been marked as 1. If the sweat had not been dyed, the result would have been marked as 0.

Static two-point discrimination

A device consisting of a washer with prongs spaced at various intervals (2, 3, 4, 6, 8, 10, 12, 15, 20, and 25 mm) about its periphery was used to measure static two-point discrimination. Prongs came into contact with the skin from great to small intervals. The test was scored by blindfolded candidates. The minimum discrimination interval was marked if the candidate had the specified feeling. The result was marked 0 if the candidate had no feelings.

Data processing and statistical analysis

Data were statistically analysed with SPSS 25.0. For continuous variables, the mean and the standard deviation were used to describe our results (\(\stackrel{-}{\text{x}}\)±s). The normal distribution and variance homogeneity tests were conducted. If the two tests’ results were satisfied, the two independent sample t-tests were used for comparisons between the two groups. One-way ANOVA was used for comparisons amongst multiple groups, and the LSD method was used for inter-group back-testing. Counts (N) and percentages (%) were used to describe summary statistics for categorical variables. The Chi-squared test or the Fisher exact probability method was used to compare group differences. All statistical analyses were two-sided tests. P < 0.05 was considered statistically significant.

Results

General information

The general data of patients in six groups were compared (Table 1). In the 0–35 days group, there were 25 male cases and 10 female cases with an average age of 36.03 ± 10.95 years (range of 17–53 years). The average size of defects was 7.81 ± 6.86 cm2 (range of 1.2–37.5 cm2). In the 36–75 days group, there were 13 male cases and 7 female cases with an average age of 38.00 ± 11.10 years (range of 17–55 years). The average size of defects was 9.78 ± 8.22 cm2 (range of 2.89–37.5 cm2). In the 76–105 days group, there were 5 male cases and 2 female cases with an average age of 40.71 ± 10.39 years (range of 22–51 years). The average size of defects was 9.23 ± 6.70 cm2 (range of 4–22 cm2). In the 106–215 days group, there were 16 male cases and 3 female cases with an average age of 31.68 ± 11.15 years (range of 17–53 years). The average size of defects was 8.90 ± 4.64 cm2 (range of 3.74–22 cm2). In the 215–265 days group, there were 11 male cases and 3 female cases with an average age of 33.50 ± 11.55 years (range of 17–53 years). The average size of defects was 6.74 ± 3.36 cm2 (range of 1.2–14.4 cm2). In the over 365 days group, there were 8 male cases and 8 female cases with an average age of 33.69 ± 13.96 years (range of 15–55 years). The average size of defects was 7.74 ± 3.40 cm2 (range of 3.6–14.4 cm2). In addition, the preoperative and postoperative conditions of the patient with a defect area of 37.5 cm2 are shown in Figure S1.

Table 1 General information on patients with free flaps at different follow-up times

Postoperative recovery

All patients were discharged after surgery treatment. No patients were necessary for secondary surgery, and all flaps survived. As shown in Table 2, all five parameters indicated statistical differences amongst the groups. With the increase in time, the recovery degree of fingerprint recognition gradually improved. The degree of recovery at 216 days after surgery was stable at about 75%. Regarding the warm and cold sensations, they also recovered significantly over time. At 1 year after surgery, 3 patients (18.8%) experienced warm intolerance, and 2 patients (15%) experienced cold intolerance; no patient experienced dysesthesia. Two-point discrimination in the 76–105 days group was worse than that in the 36–75 days group. However, as shown in Table 2, we observed that two-point discrimination gradually improved over time, even beyond the postoperative mark of the 36–75 days group (P < 0.05). The mean two-point discrimination at 1 year after surgery was 4.25 ± 2.05 mm. No patients had postoperative complications at the donor sites. The proximal interphalangeal mobility loss was less than 10 degrees. All patients returned to their jobs.

Table 2 Follow-up outcomes of patients with free flaps at different follow-up times

Example case

A 33-year-old male was admitted for emergency visits because of a crush injury due to a production accident. The finger pulp, nail fold and fingertip of his right distal index finger were the injured parts. The edges of the wound were irregular. A severe contusion of tissue with blood oozing could be observed. The tuberosity of the distal phalanx was partly exposed. The nail bed was still intact. Debridement and free fibular great toe neurovascular flap transplantation were performed after admission. Preoperative photographs of the flap transplantation are shown in Fig. 1. Figure 2 shows the immediate postoperative photographs. The patient required postoperative antibiotics, anticoagulants, antispasmodics, drugs promoting nerve growth activity and heat preservation by visible light illumination. Five days after the initial steps, the patient started rehabilitation training. Two weeks after surgery, stitches were removed, and the patient was discharged. Video 1 shows the postoperative video at 314 days, in which the fingerprint register and recognition process were recorded. Figure 3 shows postoperative photographs at 314 days, in which the appearance and results of the temperature sensation test, the autonomic nerve function test and the static two-point discrimination test were obtained. This patient demonstrated good aesthetic and functional results.

Fig. 1
figure 1

Patient’s finger injury before surgery. A, C: Preoperative view of soft-tissue defect of distal thumb. B: Design of fibular side skin flap of the great toe

Fig. 2
figure 2

Immediate postoperative view: the defect was reconstructed

Fig. 3
figure 3

Postoperative recovery of patients. A: The function and appearance of the hand site at 2 months after surgery. B: The function and appearance of the hand site at 6.5 months after surgery. C: The function and appearance of the hand site at 9 months after surgery

Discussion

Given the homology of hands and feet, toe flap transplantation is an excellent choice for repairing finger pulp defects [16, 17]. After repair, it has threads and a good appearance [18]. The repaired fingerprint also has biological recognition function, which can be used to unlock various new electronic devices. This study found that the morphology of repaired fingerprints dynamically changes as the postoperative rehabilitation process progresses. During periods 1 to 2, the fingerprint changes from deep to shallow; after the thread loses its innervation, the fingerprint does not immediately disappear and gradually becomes shallow over time. After reaching period 3, the thread gradually deepens due to the recovery of neural function. After period 5, it reaches a stable state without significant changes, so there is a deep shallow process of the thread after surgery. The cold sensation starts from nothing in period 1 and recovers faster as time shifts. The overall recovery time curve of warm sensation is 1 month later than that of cold sensation, and cold sensation is more sensitive than warm sensation. The skin has more cold receptors than heat receptors. Warm sensation gradually recovers in period 4, and its recovery speed and degree are worse than those of cold sensation.

The nerves are mainly sensory and C-type fibres [19]. The phenomenon of skin sweating is a skin reflex potential that occurs after the human body receives stimulation. It originates from the impulses released by the efferent fibres of the sympathetic nervous system, inducing synchronous activity of sweat glands [20]. Therefore, the recovery of the sympathetic nervous system can be detected through the phenomenon of sweating. In this study, we found that sweating had already begun at the beginning of period 2. By period 3, the sympathetic nerves in most of the flaps had recovered to varying degrees, and there was a significant difference compared with the depth of sensation and thread (P < 0.05) because the sympathetic nerves affected the regeneration of the surrounding meridians. The use of printing pad oil to record finger touch is a technique that has been practiced by the Chinese for thousands of years. Notably, we found that the fingerprint clarity of oil printing in periods 1, 4, 5 and 6 was the same as that in photos. However, in period 2, the camera’s photo quality and visible clarity were relatively blurry, but the fingerprints pressed out by oil printing were relatively clear, and the specific reasons need to be further studied.

Repaired fingerprints can be applied in modern life [21]. In this study, the use of mobile phone unlocking function was used to record the usage status of fingerprints. During periods 3–5, the success rate of fingerprint unlocking gradually increased. However, the repaired fingerprint shapes in different periods varied, resulting in fingerprints that could be successfully entered in period 2 but unable to be successfully unlocked again in period 3. The fingerprint had to be re-entered to successfully unlock again, and a stable state was reached in periods 4 and 5. This reason was related to the growth and shape of the finger body. As a result of functional needs, the repaired finger body may undergo local tissue remodelling and reconstruction, approaching normal finger growth. In addition, the change in two-point discrimination within different periods could be attributed to several factors: (1) Healing phase: The patients in this time frame of the 76–105 days group might have been in a specific phase of the healing process where tissue maturation and nerve regeneration could temporarily affect sensory acuity, leading to the deterioration in two-point discrimination within the 76–105 days group compared with the 36–75 days group. (2) Longitudinal improvement: Despite the setback observed in 76–105 days, our data indicated that patients experienced a gradual improvement in two-point discrimination with continued rehabilitation and as the healing process progressed. This result was consistent with the general understanding that recovery from nerve injury and sensory restoration is often a protracted process. Therefore, there is a dynamic change in the repaired finger body and fingerprint. The healing between the skin flap and the wound will result in scar formation, which starts from repair and is mainly divided into three consecutive and overlapping stages: the haemostasis/inflammation stage, the granulation tissue proliferation stage and the remodelling stage [22]. This process usually lasts 6–8 months, and the softening and stabilisation process of the subcutaneous scar can lead to changes in the surface thread [23].

In this study, some wounds require toenails to repair the nails. After period 4, the appearance and glossiness of most nails were fully restored, which was slower than the normal nail growth cycle. The anastomotic branch from the palmar digital artery to the dorsal digital artery arch and the dorsal digital artery arch from the distal end of the digital artery are the main sources of blood supply for nails [24]. A distal phalanx defect often damages the proper digital artery of the distal phalanx, leading to a decrease in direct blood supply to the nail bed [25]. This phenomenon may also be an important influencing factor for nail bed atrophy and poor glossiness.

Two methods can be used to restore and reconstruct the nerves of the skin flap: the peripheral approach and the central approach [26]. All flaps in this study were directly anastomosed to the central pathway of the sensory nerve, but their peripheral pathways also played a role in the recovery process. The use of the 4-needle epineural anastomosis technique for nerve stumps maximises nerve recovery [27]. The fibular proper artery at the base of the great toe is the main blood supply vessel for the toe flap. It is accompanied with nerves, which can minimise nerve dissociation and ischemia [28]. Therefore, all cases in this study recovered well in terms of personal sensation, and the clarity of fingerprints in the later stage was correlated with nerve recovery.

However, this study had some limitations. Firstly, this work was a single-centre study, and the same surgical team carried out all operations. Follow-up outcomes and surgeons’ skills may be intimately entwined. Secondly, the normal skin on the contralateral side of the recipient area was not tested, and the recovery of the donor sites was not recorded in detail. Lastly, a prospective randomised comparative study with other strategies is needed to yield more meaningful conclusions. In addition, there was a lack of quantitative indicators of photo sharpness. Moreover, the relationship between fingerprint shape and scar, whether there is a relationship between fingerprint shape and the utilisation rate of injured fingers at work, was not systematically studied. Furthermore, given the inconsistent compliance of postoperative patient follow-up, we did not perform dynamic pre- and post-evaluation for each patient at each period, which could have led to a degree of selective bias.

Conclusion

For the refined reconstruction of the soft-tissue injury in distal fingers, the use of free neurovascular flaps from the fibular side of great toes could achieve satisfactory outcomes.

Data availability

The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.

References

  1. Henry M. Degloving combined with structural trauma at the digital level: functional coverage with fascial free flaps. J Reconstr Microsurg. 2007;23(2):59–62.

    Article  PubMed  Google Scholar 

  2. Ulrich D, Pallua N, TREATMENT OF AVULSION INJURY OF THREE FINGERS WITH A COMPOUND THORACODORSAL ARTERY PERFORATOR FLAP INCLUDING SERRATUS ANTERIOR FASCIA. Microsurgery. 2009;29(7):556–9.

    Article  PubMed  Google Scholar 

  3. Morrison WA, Obrien BM, Macleod AM, THUMB RECONSTRUCTION WITH, A FREE NEUROVASCULAR WRAP-AROUND. FLAP FROM THE BIG TOE. J Hand Surgery-American Volume. 1980;5(6):575–83.

    Article  CAS  Google Scholar 

  4. Fulchignoni C, Rocchi L, Cauteruccio M, Merendi G. Matriderm dermal substitute in the treatment of post traumatic hand’s fingertip tissue loss. J Cosmet Dermatol. 2022;21(2):750–7.

    Article  PubMed  Google Scholar 

  5. Hahn SB, Park HJ, Kang HJ, Kang ES. Finger reconstruction with a free neurovascular wrap-around flap from the big toe. J Reconstr Microsurg. 2001;17(5):319–23.

    Article  CAS  PubMed  Google Scholar 

  6. Foucher G, Merle M, Maneaud M, Michon J. MICROSURGICAL FREE PARTIAL TOE TRANSFER IN HAND RECONSTRUCTION - A REPORT OF 12 CASES. Plast Reconstr Surg. 1980;65(5):616–26.

    Article  CAS  PubMed  Google Scholar 

  7. Rui Y, Mi J, Shi H, Zhang Z, Yan H, FREE GREAT TOE WRAP-AROUND FLAP COMBINED WITH SECOND TOE MEDIAL FLAP FOR RECONSTRUCTION OF COMPLETELY DEGLOVED FINGERS. Microsurgery. 2010;30(6):449–56.

    Article  PubMed  Google Scholar 

  8. Woo SH, Choi BC, Oh SJ, Seul JH. Classification of the first web space free flap of the foot and its applications in reconstruction of the hand. Plast Reconstr Surg. 1999;103(2):508–17.

    Article  CAS  PubMed  Google Scholar 

  9. Inigo F, Gargollo C, SECONDARY COVERAGE OF, THE HAND USING A DORSALIS-PEDIS. PLUS 1ST WEB SPACE FREE FLAP. J Reconstr Microsurg. 1992;8(6):461–5.

    CAS  PubMed  Google Scholar 

  10. Hashimoto T, Suzuki Y, Kitada M, Kataoka K, Wu S, Suzuki K, Endo K, Nishimura Y, Ide C. Peripheral nerve regeneration through alginate gel: analysis of early outgrowth and late increase in diameter of regenerating axons. Exp Brain Res. 2002;146(3):356–68.

    Article  CAS  PubMed  Google Scholar 

  11. Scheib J, Hoeke A. Advances in peripheral nerve regeneration. Nat Reviews Neurol. 2013;9(12):668–76.

    Article  CAS  Google Scholar 

  12. Yang Y, Ding F, Wu H, Hu W, Liu W, Liu H, Gu X. Development and evaluation of silk fibroin-based nerve grafts used for peripheral nerve regeneration. Biomaterials. 2007;28(36):5526–35.

    Article  CAS  PubMed  Google Scholar 

  13. Abel NA, Januszewski J, Vivas AC, Uribe JS. Femoral nerve and lumbar plexus injury after minimally invasive lateral retroperitoneal transpsoas approach: electrodiagnostic prognostic indicators and a roadmap to recovery. Neurosurg Rev. 2018;41(2):457–64.

    Article  PubMed  Google Scholar 

  14. Kornfeld T, Nessler J, Helmer C, Hannemann R, Waldmann KH, Peck CT, Hoffmann P, Brandes G, Vogt PM, Radtke C. Spider silk nerve graft promotes axonal regeneration on long distance nerve defect in a sheep model. Biomaterials 2021, 271.

  15. Schnider P, Moraru E, Kittler H, Binder M, Kranz G, Voller B, Auff E. Treatment of focal hyperhidrosis with botulinum toxin type A: long-term follow-up in 61 patients. Br J Dermatol. 2001;145(2):289–93.

    Article  CAS  PubMed  Google Scholar 

  16. Cong H-B, Chang S-M, Qiao Y-P, Wang C-L, Sui H-M, Cong L. One-stage reconstruction of complicated thumb injury with combination of microsurgical transplantations. Microsurgery. 2007;27(3):181–6.

    Article  PubMed  Google Scholar 

  17. Rui YJ, Shou KS, Zhang QR, Xu YJ, Sun ZZ, Xu L. Combined free-tissue transfer for primary reconstruction of radial part of the hand. Microsurgery. 2004;24(1):59–62.

    Article  PubMed  Google Scholar 

  18. Fan CY, Jiang J, Zeng BF, Jiang PZ, Cai PH, Chung KC. Reconstruction of thumb loss complicated by skin defects in the thumb-index web space by combined transplantation of free tissues. J Hand Surgery-American Volume. 2006;31A(2):236–41.

    Article  Google Scholar 

  19. Deglise B, Botta Y, MICROSURGICAL FREE TOE PULP TRANSFER FOR DIGITAL RECONSTRUCTION. Ann Plast Surg. 1991;26(4):341–6.

    Article  CAS  PubMed  Google Scholar 

  20. Rousseaux M, Hurtevent JF, Benaim C, Cassim F. Late contralateral hyperhidrosis in lateral medullary infarcts. Stroke. 1996;27(5):991–5.

    Article  CAS  PubMed  Google Scholar 

  21. Doi K. Microsurgical thumb reconstruction–report of six cases with a wrap-around free flap from the big toe and an iliac bone graft. Ann Acad Med Singapore. 1982;11(2):225–30.

    CAS  PubMed  Google Scholar 

  22. Korntner S, Lehner C, Gehwolf R, Wagner A, Gruetz M, Kunkel N, Tempfer H, Traweger A. Limiting angiogenesis to modulate scar formation. Adv Drug Deliv Rev. 2019;146:170–89.

    Article  CAS  PubMed  Google Scholar 

  23. Eming SA, Martin P, Tomic-Canic M. Wound repair and regeneration: mechanisms, signaling, and translation. Sci Transl Med 2014, 6(265).

  24. Usami S, Inami K, Kawahara S, Hirase Y, Shimizu H, Mori H. Investigation of predictors of successful replantation of distal digits at the nail Bed Level: the contribution of digital nerve repair to Survival Rate. Plast Reconstr Surg. 2022;149(4):889–96.

    Article  CAS  PubMed  Google Scholar 

  25. Li J, Guo Z, Zhu Q, Lei W, Han Y, Li M, Wang Z. Fingertip replantation: determinants of survival. Plast Reconstr Surg. 2008;122(3):833–9.

    Article  CAS  PubMed  Google Scholar 

  26. Hattori Y, Chuang DCC, Lan CT. Sensory restoration of the skin graft on a free muscle flap: experimental rabbit study. Plast Reconstr Surg. 2001;108(1):132–40.

    Article  CAS  PubMed  Google Scholar 

  27. Engelhardt TO, Rieger UM, Schwabegger AH, Pierer G. Functional resurfacing of the palm: flap selection based on defect analysis. Microsurgery. 2012;32(2):158–66.

    Article  CAS  PubMed  Google Scholar 

  28. Gkotsi A, Wirtz R, Schuind F. Microvascular reconstructive techniques in orthopaedic traumatology. Injury-International J Care Injured. 2019;50:S84–7.

    Article  Google Scholar 

Download references

Acknowledgements

This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

Funding

This research received no specific grant from any funding agency in the public, commercial or not-for-profit sectors.

Author information

Authors and Affiliations

Authors

Contributions

FNY performed the research design and wrote the manuscript with revision, guidance, and feedback from CX and LJL. The acquisition of data and proofreading of this manuscript were performed by FNY and FX. Data analysis and interpretation were performed by FNY, FX, GRP, GL, WSW. FNY and FX put a lot of energy into the process of revising paper. CX and LJL gave guidance to paper during the process of revising paper. All authors have read and approved the final version of the manuscript.

Corresponding authors

Correspondence to Chao Xie or Lijun Lin.

Ethics declarations

Ethics approval and consent to participate

This study was conducted by the Declaration of Helsinki and was approved by the Ethics Committee of Guzhen People’s Hospital (Approval ID: GZLLPS 20180109-01). All patients gave their informed consent for inclusion before they participated in the study. Written informed consent was obtained from all the participants. The study was conducted at Guzhen People’s Hospital, where all surgical procedures were performed. All operations were carried out by the same surgical team, led by the first author, Dr. Fengnian Yu. Dr. Fengnian Yu was affiliated with Guzhen People’s Hospital at the time of the study. Subsequently, as of August 1, 2023, Fengnian Yu has moved to Jiangmen People’s Hospital.

Consent for publication

Written informed consent for publication of identifying images or other personal or clinical details was obtained from all of the participants.

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary Material 1

Supplementary Material 2

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Yu, F., Xiao, F., Peng, G. et al. Repair of distal finger soft-tissue defects with free fibular great toe neurovascular flaps. BMC Musculoskelet Disord 25, 479 (2024). https://doi.org/10.1186/s12891-024-07563-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12891-024-07563-2

Keywords