4/2010
vol. 48
Original article Comparison of the results of surgical treatment after direct neurorrhaphy and reconstruction with sural nerve grafts in perinatal brachial plexus lesions
Folia Neuropathol 2010; 48 (4): 270-275
Online publish date: 2010/12/17
Get citation
Introduction The choice of proper microsurgical technique during primary reconstructive operations depends on the intraoperative view [8,13]. Postganglionic lesions with total rupture of neural elements (fifth degree of injury on Sunderland’s scale) require microsurgical direct neurorrhaphy [5,12] or reconstruction with autogenic cutaneous nerve grafts [7,10,17]. The following nerves are used as grafts: sural nerve, cutaneous medial brachial and antebrachial nerve, lateral cutaneous antebrachial nerve, superficial branch of radial nerve, and supraclavicular nerves [2,3,16]. Microsurgical anastomosis can be performed using sutures or fibrin glue [7,9,10,17]. Material and methods The clinical material consisted of 14 children of both sexes treated surgically in the period of 1996-2005 because of postganglionic brachial plexus lesion (fifth degree on Sunderland’s scale). The following surgical procedures were performed: in 8 cases direct neurorrhaphy and in 6 cases reconstruction with sural nerve grafts. Clinical type of injury, location of postganglionic lesion and detailed description of microsurgical techniques are presented in Tables I and II.
Intraoperatively during resections non-conducting parts of proximal stumps of ruptured nerve elements were collected as material for histopathological examinations. The results of surgical treatment (after a minimum 3-year observation period) were evaluated using the following scales:
1) Gilbert’s scale for evaluation of shoulder function [10]:
stage 0 = flail shoulder,
stage I = abduction or flexion to 45°, no active lateral rotation,
stage II = abduction < 90°, lateral rotation to neutral,
stage III = abduction = 90°, weak lateral rotation,
stage IV = abduction < 120°, incomplete lateral rotation,
stage V = abduction > 120°, active lateral rotation,
stage VI = normal.
2) Gilbert and Raimondi scale for evaluation of elbow function [10]:
A. Elbow flexion:
nil or some contraction = 1,
incomplete flexion = 2,
complete flexion = 3.
B. Elbow extension:
no extension = 0,
weak extension = 1,
good extension = 2.
C. Extension deficit:
0-30° = 0; 30-50° = –1,
More than 50° = –2.
3) Al-Qattan’s scale for evaluation of forearm rotation moves [1]:
1 = pronated forearm causing a functional or cosmetic disability,
2 = supinated forearm causing a functional or cosmetic disability,
3 = functional forearm position (mid pronation-supination or slight pronation) with no or
minimal active motion,
4 = same as 3 but with good active pronation and supination,
5 = normal power and range of motion.
4) Al-Qattan’s scale for evaluation of wrist function [1]:
0 = no contraction or flicker of contraction,
1 = active movement with gravity eliminated,
2 = active movement against gravity only,
3 = active movement against resistance with motion reaching ≤ 1/2 of normal range,
4 = active movement against resistance with motion reaching > 1/2 of normal range,
5 = normal power and range of motion.
5) Al-Qattan’s scale for evaluation of hand motor function [1]:
0 = useless hand – complete paralysis or slight finger motion of no use, useless thumb,
1 = poor function – only very weak grip possible,
2 = fair function – there is some active flexion and/ or extension of the fingers and some
thumb mobility but the hand posture is intrinsic minus,
3 = good function – same as 2 but there is no intrinsic minus posture (intrinsic balance),
4 = excellent function – near normal active finger flexion/extension and thumb mobility, with some active intrinsic function,
5 = normal function.
6) BMRC scale modified by Omer and Dellon for evaluation of hand sensory function [4,15] – only in total palsies.
During assessment of treatment results the effect of tenomyoplasty performed in some cases, indicated in Tables III and IV as (T), was also taken into consideration. Results The results of surgical treatment are presented in Tables III and IV. Discussion In postganglionic lesions with total rupture of nerve elements in our material we performed direct neurorrhaphy or reconstruction with sural nerve grafts. The possibilities of using direct neurorrhaphy in reconstructions of brachial plexus are, according to some authors, significantly limited [6,17,18]. It is obvious that use of this technique requires compliance with some specified conditions [11,14]. The lack in continuity of neural elements must be short. Adequate stump resection is necessary, because too restricted excision of damaged elements is one cause of failure in nerve reconstructions. Intraoperatively, in cases of rupture of brachial plexus trunks, we did not observe in the proximal stumps macroscopic features of neuroma, similar to neuromas formed after peri-pheral nerve sections (Figs. 1 and 2). It may cause difficulties in determining the range of resection. The excision of fibrous scar tissue (Fig. 3) and pathologically changed neural tissue is necessary (Figs. 4-6). The most important condition for success of this method is the possibility to perform anastomosis without any tension in the suture line (Fig. 7). The results that we achieved using direct neurorrhaphy in our material do not disqualify this surgical technique. This technique, after fulfilling all discussed conditions, is in our opinion very useful in primary reconstructive procedures in brachial plexus lesions. This is confirmed by the results reported by Kirjavainen and co-workers. They achieved the best results in operative treatment of brachial plexus injuries after using direct neurorrhaphy [12]. The possibility of reconstruction with direct neurorrhaphy informs indirectly about the smaller range of brachial plexus injury. The lack of continuity in neural elements which requires the use of autogenic nerve grafts is evidence for a greater range of brachial plexus injury. In our material in 8 cases in which direct neurorrhaphy was performed the gap between neural elements varied from 0.7 to 1.0 cm. A greater lack in continuity required the use of sural nerve grafts. The number of grafts was between 2 and 4, and their length was between 1 and 3 cm. In one case (Case 2, Table II) the possibility of mobilization of nerve stumps was limited and a decision in favour of reconstruction with sural nerve grafts was taken. In our opinion both applied methods are useful in surgical treatment of perinatal brachial plexus lesions.
Conclusion: Direct neurorrhaphy is, in some favourable conditions, a useful technique in surgical treatment of perinatal brachial plexus injuries. The possibility of using this method indicates on less extension of the brachial plexus lesion. References 1. Al-Qattan MM. Assessment of the motor power in older children with obstetric brachial plexus palsy. J Hand Surg 2003; 28B: 46-49.
2. Al-Qattan MM. Identification of the phrenic nerve in surgical exploration of the brachial plexus in obstetrical palsy. J Hand Surg 2004; 29A: 391-392.
3. Anand P, Birch R. Restoration of sensory function and lack of long-term chronic pain syndromes after brachial plexus injury in human neonates. Brain 2002; 125: 113-122.
4. Dellon AL. The moving two-point discrimination test: clinical evaluation of the quickly-adapting fiber-receptor system. J Hand Surg 1978; 3: 478-481.
5. Giele H. Management of obstetrical brachial plexus palsy. Curr Paediatr 1999; 9: 182-187.
6. Gilbert A. Long-term evaluation of brachial plexus surgery in obstetrical palsy. Hand Clin 1995; 11: 583-594.
7. Gilbert A. Results of brachial plexus surgery and replacement operations in traumatic brachial plexus birth injury – induced paralysis. Orthop 1997; 26: 723-728.
8. Gosk J, Rutowski R, Rabczyński J. The analysis of the intrasurgical view of the obstetric brachial plexus palsy. Folia Neuropathol 2005; 43: 143-147.
9. Gosk J, Knakiewicz M, Wiącek W, Reichert P. Wykorzystanie kleju fibrynowego w rekonstrukcjach nerwów obwodowych. Polim Med 2006; 36: 11-15.
10. Haerle M, Gilbert A. Management of complete obstetric brachial plexus lesions. J Pediatr Orthop 2004; 24: 194-200.
11. Haftek J. Autogenes cable nerve grafting instead of end to end anastomosis in secondary nerve suture. Acta Neurochir 1976; 34: 217-227.
12. Kirjavainen M, Remes V, Peltonen J, Kinnunen P, Pöyhia T, Telaranta T, Alanen M, Helenius I, Nietosvaara Y. Long-term results of surgery for brachial plexus birth palsy. J Bone Joint Surg 2007; 89A: 18-26.
13. Knakiewicz M, Rutowski R, Gosk J, Kuryszko J, Kielan W, Rudno-Rudzińska J, Knakiewicz M. The evaluation of the influence of a high injury to brachial plexus elements on the condition of neurons of the anterior horns of the spinal cord – experimental research. Folia Neuropathol 2009; 47: 347-353.
14. Malessy MJ, van Duinen SG, Feirabend HKP, Thomeer RTWM. Correlation between histopathological findings in C5 and C6 nerve stumps and motor recovery following nerve grafting for repair of brachial plexus injury. J Neurosurg 1999; 91: 636-644.
15. Omer GE. Report of the Committee for evaluation of the clinical result in peripheral nerve injury. J Hand Surg 1983; 8: 754-758.
16. Piatt JH. Birth injuries of the brachial plexus. Pediatr Clin N Am 2004; 51: 421-440.
17. Slooff ACJ. Obstetric brachial plexus lesions and their neurosurgical treatment. Microsurg 1995; 16: 30-34.
18. Waters PM. Update on management of pediatric brachial plexus palsy. J Pediatr Orthop 2005; 25: 116-126.
Copyright: © 2010 Mossakowski Medical Research Centre Polish Academy of Sciences and the Polish Association of Neuropathologists. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License ( http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
|
|