- Case report
- Open Access
Free functional gracilis muscle transfer in children with severe sequelae from obstetric brachial plexus palsy
© Bahm and Ocampo-Pavez. 2008
- Received: 29 April 2008
- Accepted: 30 October 2008
- Published: 30 October 2008
We present 4 children between 6 and 13 years suffering from severe sequelae after a total obstetric brachial plexus lesion resulting in a hand without functional active long finger flexion. They had successfully reanimated long finger flexion using a free functional gracilis muscle transfer. These children initially presented a total obstetric brachial plexus palsy without neurotisation of the lower trunk in an early microsurgical nerve reconstruction procedure.
We describe our indications for this complex microsurgical procedure, the surgical technique and the outcome.
Obstetric brachial plexus palsy may result in a severe impairment of upper limb function. Early microsurgical reconstruction is proposed in upper and total palsies with insufficient functional recovery . Nevertheless, major motor functions may not recover, both in operated or not operated children.
Free functional muscle transfer has been developed in the last 30 years to replace major muscle function, especially in the face and the upper limb [2, 3]. Volkmann's ischemic contracture, tumor resection, and extensive palsy are possible indications.
An isolated motor deficit in a major upper limb function in children suffering from obstetric brachial plexus palsy might be corrected by means of a free muscle transfer, using the gracilis muscle. Finger and elbow flexion are obvious primary goals. These were also the indications where we decided to apply this technique.
We present our strategy, indications, operative technique and results.
We also report the advantages of this microsurgical procedure, but also technical drawbacks and reasonable limits of indication.
Historical background 
The experimental background was set in 1970 when Tamai  reported the first successful transplantation of a rectus femoris muscle to the forelimb of a dog, using microneurovascular techniques.
The first clinical case was published 3 years later, when Chinese surgeons  transplanted part of a pectoralis major muscle to improve the hand function of a patient with Volkmann's ischemic contracture.
In the field of brachial plexus reconstruction, Doi  presented a new approach using two free gracilis muscle transfers to reconstruct major upper limb motors, and an extensive and impressive clinical series in children was recently published by Chuang .
Our clinical series includes 900 children with obstetric brachial plexus palsy treated in our unit between 1997 to 2007, and about 150 microsurgical plexus reconstructions. In 7 cases suffering very severe total brachial plexus palsy without recovery of functional active long finger flexion (all 7), we performed a free gracilis muscle transfer, six for long finger flexion, one for biceps replacement.
Clinical background of the operated children
brachial plexus exploration, reconstruction of the upper and middle trunk, neurolysis of the lower trunk.
extraplexic neurotisation SAN to ulnar nerve, without success
Normal MRI, EMG shows only reinnervation of arm muscles, no recovery within forearm and hand.
MyeloCT: suspicion of root avulsions C6 C8 Th1
no previous surgery
MyeloCT: suspicion of root avulsion C7 C8
EMG: no activity C6 C7 C8 Th1
plexus exploration, only neurolysis C5
Before surgery, all children had recovered active wrist and finger extension, which are both mandatory requirements prior to surgery to stabilize the wrist and allow finger release. Otherwise, the transplanted muscle would rather flex the wrist and finger flexion would be weak.
Due to the extensive palsy, no local (forearm) muscles were available for a tendon or muscle transfer to improve the finger flexion.
Examination methods, video recording
All children had a complete motor assessment before and after surgery. All surgeries were carried out once the anaesthesiologist had independently checked the children, especially for airway infections or fever of unknown origin (both criteria excluded a long lasting elective surgery under general anesthesia).
Video-recording was performed before and after surgery.
There were always three operative steps: The motor nerve donor (spinal accessorius nerve SAN) was identified and prolonged to the volar forearm level by a sural graft.
To make sure that nerve regeneration had occurred down to the distal end of the transplanted nerve, one or more nerve biopsies were taken to analyse the proportion and quality of newly myelinated nerve fibers. Only when the neuropathologist was convinced with a good regenerative capacity ie a substantial proportion of newly myelinated fibers, than the microsurgical transfer was performed in a 2 team approach.
Step1: preparing the motor nerve
The SAN is identified through a routine supraclavicular transverse approach. The nerve is identified lateral to the brachial plexus area, in the subcutaneous space and followed down to its entrance into the trapezius muscle. The first motor collateral branch for the horizontal muscle part is spared, and the second larger branch running down is sectioned as distally as possible. An autologous sural nerve is harvested by routine step-cut incisions on the posterior leg and then coapted to the SAN by 10/0 microsutures in an antidromic direction after having passed the graft through a subcutaneous tunnel in the anterior arm.
The distal end of the sural nerve is buried in the muscle remnants at the proximal volar forearm level, and two non absorbable stitches mark the level of the nerve – muscle coaptation.
The arm is immobilized for 10 days in a sling and the child is discharged after 3 days.
Step2: nerve biopsy
After 8 to 12 months, a nerve biopsy is performed at the proximal forearm level and sent for neuropathological examination. Slices are examined to determinate the proportion and quantity of myelinated fibers.
If the biopsy reveals an insufficient reinnervation quality, a new biopsy is conducted 3 months later, and meanwhile the nerve is buried again in the muscular bulk.
Step3: free functional muscle transfer in 2 teams
When the recipient site is ready with its vessels well prepared, the muscle harvest is completed by the division of the neurovascular bundle of the gracilis muscle and ischemia time is documented.
The flexed fingers and the wrist in neutral position are immobilized in a dorsal forearm splint for 6 weeks.
We realized the free functional muscle transfer once the nerve biopsy showed sufficient regeneration, i.e. 9–14 months after the sural nerve transplant.
Every patient underwent 4 weeks postoperatively an angioMRI to check good vascular supply into the transposed muscle and an elective EMG at about 6 months.
The decision for the free muscle transfer was taken after one nerve biopsy in all children but one, where a second biopsy was mandatory six months later to show a sufficient reinnervation pattern. The first child had previously a SAN to ulnar nerve neurotisation at the proximal forearm level using a saphenous graft. In this case, the biopsy and the later nerve coaptation were made directly on the distal graft which was separated from the ulnar nerve.
In one other child, we observed one progressive monitor skin necrosis starting on the second day after surgery. Reexploration showed a patent vascular anastomosis and viable muscle tissue, so the skin island was removed.
In the other cases, no vascular disturbances were seen in the follow- up.
The angioMRI showed good vascularisation of the transferred muscle, before contractile activity begun.
Results after free gracilis muscle transfer
Delay to beginning muscle function:
Function (global grasp):
M3 in 3 of 4 children
For a mean follow-up of 2 years, we observed no weakness in the successfully reanimated hands.
There was one failure, and we reoperated that child 18 months later. The muscle was still present, but had undergone hypotrophy. We believe that either the regenerative capacity of the nerve graft or the nerve coaptation were insufficient. The remaining atrophied muscle tissue was well vascularised, although the pedicle could not be identified clearly. This child is actually scheduled for a new transfer.
Other teams published successful cases, but details on results are rarely mentioned. Zuker and Manktelow  have experience in 30 forearm reconstructions with beginning muscle contraction as soon as 2 months after surgery. More than half of their patients were able to make a fist completely. The distal palmar crease-to-fingertip distance ranged from 0.5 to 4 cm in adults and was less good in children. Grip strength reached 38% of the normal side but 25% in children.
A good motor nerve connected with the shortest distance to a healthy and strong muscle which is adapted to the functional demand may result in a successfully reanimated major limb function. The reinnervation quality of the donor nerve could be followed by a progressing Hoffmann-Tinel sign along the anterior arm, but a qualitative assessment is only possible through histopathologic studies. The possibility of quantitative assessment of motor fiber content in the donor nerve is still under discussion .
Technical considerations in pediatric microsurgery refer to the vessel diameter (which might be 0.6 mm), the intraoperative conditions of fluid balance, blood tension and temperature (as in adult free flaps) and the technique of vascular and neural (micro)anastomosis, using 10/0 sutures.
As we observed one skin island necrosis with patent vascular anastomosis, obviating an unreliable monitor island, we furtheron include the whole fascia around the gracilis muscle as described by Addosooki et al  who reported on a 100% reliable skin monitor island.
Indications for this complex reconstructive procedure must be carefully established together with the child and the parents. Eventual alternatives, like pedicled muscle flaps, eg the brachialis muscle transfer described by Bertelli  must be discussed and risks and drawbacks must be outlined.
The donor site morbidity for the muscle harvest is minor, but the choice of the donor nerve might be critical, as other collegues would not hesitate to take the whole phrenic nerve to neurotise a free gracilis transfer even in young children and for a "minor" motor function like active finger extension . Although this shows evidence of a high level of technical expertise, our general and cultural background would forbid these reconstructive procedures, where a reanimated minor function (eg wrist or finger extension) is reestablished harvesting a main motor nerve and damaging a major vital muscle like the hemidiaphragm in a young and growing child.
Neuropathologic assessment of the regenerative quality of the transplanted nerve by new techniques using a reliable motor fiber assessment (choline acetyl transferase activity)  could help to increase the prognostic value.
The knowledge of this microsurgical option should increase in the general pediatric and orthopaedic community, as it may be the only true solution to enhance function in a really useful manner.
The microsurgical risk remains a constant problem due to anatomical variations and technical failures.
The parents of the children who underwent these surgeries documented by photographs and video sequences pre-, per- and postoperatively were informed about the present publication and acknowledged the use of photo and film material.
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