|
|
|
|
The Internet Journal of Orthopedic Surgery™ ISSN: 1531-2968| Home | Editors | Current Issue | Archives | Instructions for Authors | Disclaimer |Routine pre-operative bone biopsy in non-union of long bones: analysis of 26 casesRelated Articles
NS Motsitsi
HM van Niekerk
Citation: N. Motsitsi & H. van Niekerk : Routine pre-operative bone biopsy in non-union of long bones: analysis of 26 cases. The Internet Journal of Orthopedic Surgery. 2009 Volume 13 Number 1 Keywords: routine biopsy | non-union | long bones Table of ContentsAbstractBackground. Non-union of long bones is relatively rare, yet remains one of the most challenging complications to treat. The presence or absence of infection influences the adopted surgical strategy. Biological disturbances in aseptic non-union are also different from those encountered in cases of infected non-union. The purpose of this paper is to determine whether a pre-operative bone biopsy should be done in all cases of non-union of long bones. IntroductionThere are myriads of operative and non-operative treatment methods for fractures of long bones. The majority of long bones will unite when managed according to current orthopaedic practices. The rate of non-union varies greatly among studies1 yet, over all, the rate of non-union is less than 1%. Non-union is a formidable challenge to manage. Of course, the presence or absence of infection influences the treatment approach because the biological disturbances in aseptic cases are different from those where sepsis does occur.2,3 A good mechanical environment can restore the disturbed biology, whereas in septic cases the disturbed biology is characterized by tissue necrosis and ischaemia. The question whether a pre-operative bone biopsy should be done routinely in all cases of non-union of long bones, or not, is not clearly documented in the English literature on the subject. The purpose of this paper is to determine whether this should be the case. Materials and methodsSetting: A secondary hospital affiliated with a tertiary institution. Subjects: Twenty-six consecutive adult patients. The study was done over nineteen months (February 2007 - August 2008). The detailed information was extracted using a pro forma (see Table 1).
Type of study: Retrospective. Approval by an ethics committee is not needed for retrospective studies. [Pre-operative biopsies are done per departmental protocol.] Clinical classification: All patients were classified clinically according to Athanasou et al into the following categories: 4 Group I = clean or aseptic Group II = suspicious of infection Group III = clinically infected Prerequisites before the biopsy Every patient must have been off antibiotic treatment for at least six weeks prior to the biopsy. A full blood count, the Erythrocyte Sedimentation Rate (ESR) and C-reactive Protein (CRP) must be obtained just before the biopsy. Technical considerations Three tissue specimens must be taken from different areas of the fracture site. Cultures must include anaerobes. Measuring the outcome For the result to be considered positive, cultures of at least two specimens must contain the same organism(s). ResultsThere were 21 males and 5 females in the test group. Their average age was 39 years (range: 20 - 65). Seven patients presented initially with closed fractures. The number of patients per group was as follows: Group I (n = 6), Group II (n = 19) and Group III (n = 1). Inflammatory markers were: CRP (average), Group I = 11.1 mg/l (range < 1 - 34.5), Group II = 14.1 mg/l (range <1 - 67.5) and Group III = 22 mg/l (one subject). ESR (average), Group I = 29.7 mm/hr (0-140), Group II = 27.0 (0-112) and Group III = 18 (only one subject). In some of the cases, some of the inflammatory markers were not recorded. The positive culture results, recorded according to clinical groups, were as follows: Group I = 1, Group II = 2 and Group III = 0. The complete demographic data and results are recorded in Table 2.
DiscussionOur results suggest that a pre-operative biopsy should be seriously considered in cases of non-union. Positive cultures were found in groups I and II. These results changed our management strategies. The inflammatory markers did not differ significantly from one group to the other. Group III could not be directly compared to the other groups because there was only one patient in this group. Culture results could not be predicted on the basis of inflammatory markers. Patient 26 needs some special consideration because he presented to us with actively draining sinus from the tibia. Previous culture results from the abscess (done by another institution) cultured Methicillin-resistant Staphylococcus Aureus (MRSA). The patient showed us the results and sensitivity. Cultures obtained intra-operatively during bone and soft-tissue debridement cultured the same organism, rendering the sensitivity results exactly the same. This raises the possibility that there may be other explanations for our negative results, namely The source of infection could be soft tissue. The osteomyelitis could be patchy and therefore a “blind” bone biopsy could give false negative results. Infection is a known cause of non-union and is of particular concern in patients with a history of open fractures or multiple surgical procedures.5 Surgical intervention (open reduction and internal fixation) in septic non-union can lead to persistent infection in up to 66% of cases.6 The role of a pre-operative biopsy is hardly discussed in detail in English literature on the subject. DR Marsh et al did intra-operative biopsies in all 56 of their patients treated by open means.7 This practice is also advocated by Bellabarba et al.8 They gave no further details of their findings. KM Emara emphasized that infection should be excluded in all cases of non-union but gave no details of his results.3 The accuracy of a “blind” pre-operative bone biopsy can be significantly increased by pre-operative sequential scintigraphy using 99mTc-MDP (technetium – 99m methylene diphosphonate) / 111Indium-white blood cells (111In-WBC). This investigation is very useful in detecting osteitis at a fracture non-union site.5 It can also distinguish between soft-tissue and bone infection. The other alternative is 111In-WBC that has a 100% sensitivity, specificity and negative predictive value.9 A Biopsy can then be done in an area of increased uptake. Magnetic resonance imaging (MRI) is also a very good modality that can distinguish between soft- tissue and bone infection. The limitations of our study are its retrospective nature and the small number of patients reviewed. A larger and well-powered prospective study is required. Correspondence toDr NS Motsitsi References1. Tzioupis C, Giannoudis PV. Prevalence of long-bone non-unions. Injury, Int. J. Care Injured 2007; 385: 53- 59. (s) 2. Wiss DA, Stetson WB. Tibial non-union: Treatment alternatives. Journal of American Academy of Orthopaedic Surgeons 1996; 4(5, September/October): 249-257. (s) 3. Emara KM. Ilizarov technique in management of nonunited fracture of both bones of the forearm. J. Orthopaed Traumatol 2002; 3: 100-180. (s) 4. Motsitsi NS. Management of infected nonunion of long bones: The last decade (1996-2006). Injury, Int. Care Injured 2008; 39: 155- 160. (s) 5. Seabold JE, Nepola JV, Conrad GR, Marsh JL, Montgomery WJ, Bricker JA, Kirchner, PT. Detection of osteomyelitis at fracture nonunion sites: comparison of two scintigraphic methods. ARJ 1989; Vol 152, (5), 1021 -1027. (s) 6. Struijs P, Poolman RW, Bhandari M. Infected nonunion of the long bones. J. Orthop Trauma 2007; 21(7, August): 507-511. (s) 7. Marsh DR, Shah S, Elliot J, Kurdy N. The Ilizarov method in nonunion, malunion and infection of fractures. JBJS 1997; 79-B(2, March): 273- 279. (s) 8. Bellabarba C, Ricci WM, Bolhofner BR. Indirect reduction and plating of distal femoral nonunions. Journal of Orthopaedic Trauma. 2002,16(5): 287-296. (s) 9. Esterhai JL, Stephen JR, Goll R, McCarthy KE, Velchik M, Alavi A, Brighton CT, Heppenstall RB. Indium-111 Leukocyte scintigraphic detection of sub-clinical osteomyelitis complicating delayed and nonunion long bone fractures: a prospective study. Journal of Orthopaedic Research 1987; 5(1): 1-6. (s) This article was last modified on Wed, 13 May 09 18:31:42 -0500 This page was generated on Fri, 19 Mar 10 00:22:15 -0500, and may be cached. |
|
Home |
Journals |
Sponsors |
Books |
PubMed |
Editorial Help |
Privacy Policy |
Disclaimer |
Job Opportunities |
Contact
Copyright Internet Scientific Publications, LLC., 1996 to 2010. |
|