ACUTE AND CHRONIC OSTEOMYELITIS

Transcription

1 ACUTE AND CHRONIC OSTEOMYELITIS

2 DEFINITION Inflammation of the bone caused by an infecting organism

3 HISTORY In the early 1900 s about 20% of patients with osteomyelitis died and patients who survived had significant morbidity.

4 Introduction- Oldest known evidence of osteomyelitis fractured spine of dimetrodon permian reptile million years ago Hippocrates BC infection after fracture Nelaton credited with introducing the term osteomyelitis in

5 INTRODUCTION The key to successful management is early diagnosis and appropriate surgical and antimicrobial treatment. A multi disciplinary approach is required, involving an orthopaedic surgeon, an infectious disease specialist, and a plastic surgeon in complex cases with significant soft tissue loss.

6 CLASSIFICATION 1) The duration - acute, subacute and chronic 2) Mechanism of infection exogenous or hematogenous 3) The type of host response to the infection- pyogenic or non pyogenic

7 ACUTE HEMATOGENOUS OSTEOMYELITIS Most common type of bone infection, usually seen in children Decrease in incidence, could be due to higher standard of living and improved hygiene. Bimodal distribution- younger than 2 years, and 8-12 years More common in males

8 ACUTE HEMATOGENOUS OSTEOMYELITIS- CAUSES Caused by a bacteraemia Bacteriological seeding of bone generally is associated with other factors such as localized trauma, chronic illness, malnutrition or an inadequate immune system.

9 ACUTE HEMATOGENOUS OSTEOMYELITIS PATHOPHYSIOLOGY In children the infection generally involves the metaphyses of rapidly growing long bones Bacterial seeding leads to an inflammatory reaction which can cause local ischaemic necrosis of bone and subsequent abscess formation

10 ACUTE HEMATOGENOUS OSTEOMYELITIS PATHOPHYSIOLOGY As the abscess enlarges, intramedullary pressure increases causing cortical ischaemia, which may allow purulent material to escape through the cortex into the subperoisteal space.

11

12 ACUTE HEMATOGENOUS OSTEOMYELITIS PATHOPHYSIOLOGY A subperisoteal abscess then develops If left untreated this process eventually results in extensive sequetra formation and chronic osteomyelitis

13 ACUTE HEMATOGENOUS OSTEOMYELITIS PATHOPHYSIOLOGY In children younger than 2 years, blood vessels cross the physis, thus epiphysis may be involved Limb shortening or angular deformity may occur

14 ACUTE HEMATOGENOUS OSTEOMYELITIS PATHOPHYSIOLOGY Joint may be involved in some caseship joint most common, especially for intraarticular physes- proximal humerus,radial neck, distal fibula Metaphysis has relatively fewer phagocytic cells than the physis or diaphysis, hence more infection here

15 ACUTE HEMATOGENOUS OSTEOMYELITIS PATHOPHYSIOLOGY In children older than 2 years the physis effectively acts as a barrier to the spread of a metaphyseal abscess Metaphyseal cortex thicker, hence diaphysis more at risk After physes are closed acute hematogenous osteomyelitis is much less common

16 ACUTE HEMATOGENOUS OSTEOMYELITIS PATHOPHYSIOLOGY After the physes are closed, infection can extend directly from the metaphysis into the epiphysis and involve the joint Septic arthritis resulting from acute hematogenous osteomyelitis generally is seen only in infants and adults.

17 ACUTE HEMATOGENOUS OSTEOMYELITIS MICROBIAL PATTERN Staphylococcus aureus most common in older children and adults Gram negative bacteria- increasing trend- vertebral Pseudomonas most common in intravenous drug abusers Salmonella in sicke cell Fungal infections in chronically ill patients on long term intravenous therapy.

18 ACUTE HEMATOGENOUS OSTEOMYELITIS MICROBIAL PATTERN Infants- staph aureus most common but group B streptococcus and gram negative coliforms Prematures staph aureus andgram negative organisms Hemophilus influenzae primarily in children 6 months to 4 years old, incidence decreased dramatically by

19 ACUTE HEMATOGENOUS OSTEOMYELITIS MICROBIAL PATTERN Ngetich, 2002 found that of children presenting with haematogenous osteomyelitis in Kenyatta national hospital the commonest isolated organism was staphylococcus aureus accounting for 29 (60.4%)of the cases, 15 (60%) of these were MRSA strains

20 ACUTE HEMATOGENOUS OSTEOMYELITIS DIAGNOSIS History and physical examination Fever and malaise Pain and local tenderness Sweliing Compartment syndrome in children

21 ACUTE HEMATOGENOUS OSTEOMYELITIS DIAGNOSIS Laboratory tests White blood cell count Erythrocyte sedimentation rate C-reactive protein checked very 2-3 days post treatment initiation Aspiration for suspected abscess

22 ACUTE HEMATOGENOUS OSTEOMYELITIS DIAGNOSIS Plain radiographs Technetium-99m bone scan +/- MRI

23 RADIOGRAPHS Soft tissue swelling Periosteal reaction Bony destruction (10-12 days)

24 BONE SCAN Can confirm diagnosis hrs after onset

25 ACUTE HEMATOGENOUS OSTEOMYELITIS TREATMENT Surgery and antibiotic treatment are complementary, in some cases antibiotics alone may cure the disease. Choice of antibiotics is based on the highest bacteriocidal activity, the least toxicity and the lowest cost

26 ACUTE HEMATOGENOUS OSTEOMYELITIS TREATMENT Nade s 5 principles of treatment 1. An appropriate antibiotic is effective before pus formation 2. Antibiotics do not sterilize avascular tissues or abscesses and such areas require surgical removal

27 ACUTE HEMATOGENOUS OSTEOMYELITIS TREATMENT- NADES PRINCIPLES 3. If such removal is effective, antibiotics should prevent their reformation and primary wound closure should be safe 4. Surgery should not damage already ischaemic bone and soft tissue 5. Antibiotics should be continued after surgery

28 ACUTE HEMATOGENOUS OSTEOMYELITIS TREATMENT The two main indications for surgery in acute hematogenous osteomyelitis are: 1. The presence of an abscess requiring drainage 2. Failure of the patient to improve despite appropriate intravenous antibiotic treatment

29 ACUTE HEMATOGENOUS OSTEOMYELITIS TREATMENT- SURGERY The objective of surgery is to drain any abscess cavity and remove all non viable or necrotic tissue Subperiosteal abscess in an infant-several small holes drilled through the cortex into the medullary canal If intramedullary pus is found, a small window of bone is removed Skin is closed loosely over drains and the limb splinted

30 ACUTE HEMATOGENOUS OSTEOMYELITIS TREATMENT Generally a 6 week course of intravenous antibiotics is given Orthopedic and infectious disease followup is continued for at least 1 year

31 SUBACUTE HEMATOGENOUS OSTEOMYELITIS More insidious onset and lacks severity of symptoms Indolent course hence diagnosis delayed for more than two weeks.

32 SUBACUTE HEMATOGENOUS OSTEOMYELITIS CLINICAL FEATURES The indolent course of subacute osteomyelitis is due to: increased host resistance decreased bacterial virulence administration of antibiotics before the onset of symptoms Systemic signs and symptoms are minimal Temperature is only mildly elevated Mild to moderate pain

33 SUBACUTE HEMATOGENOUS OSTEOMYELITIS INVESTIGATIONS White blood cell counts are generally normal ESR is elevated in only 50% of patients Blood cultures are usually negative Plain radiographs and bone scans generally are positive

34 SUBACUTE HEMATOGENOUS OSTEOMYELITIS INVESTIGATIONS S. Aureus and Staphylococcus epidermidis are the predominant organisms identified in subacute osteomyelitis

35 SUBACUTE HEMATOGENOUS OSTEOMYELITIS BRODIE ABSCESS Localized form of subacute osteomyelitis occuring most commonly in the long bones of the lower extremeties Intermittent pain of long duration is most times the presenting compliant, along with tenderness over the affected area

36 BRODIE ABSCESS

37 SUBACUTE HEMATOGENOUS OSTEOMYELITIS BRODIE ABSCESS On plain radiographs appears as a lytic lesion with a rim of sclerotic bone S aureus is cultured in 50% of patients and in 20% the culture is negative The condition requires open biopsy with curetage to make the diagnosis The wound should be closed loosely over a drain

38 SUBACUTE HEMATOGENOUS OSTEOMYELITIS GLEDHILL CLASSIFICATION

39 SUBACUTE HEMATOGENOUS OSTEOMYELITIS TREATMENT Biopsy and curettage followed by treatment with appropriate antibiotics for all lesions that seem to be aggressive For lesions that seem to be a simple abscess in the epiphysis or metaphysis biopsy is not recommended- IV antibiotics for 48 hrs followed by a 6 week course of oral antibiotics

40 CHRONIC OSTEOMYELITIS Hallmark is infected dead bone within a compromised soft tissue envelope The infected foci within the bone are surrounded by sclerotic, relatively avascular bone covered by a thickened periosteum and scarred muscle and subcutaneous tissue

41 COM Sinus track cultures usually do not corelate with cultures obtained at bone biopsy

42 COM IN KNH 2008-= = = = = 53

43 CLASSIFICATION OF COM

44 ANATOMICAL CLASSIFICATION

45 CLASSIFICATION OF COM

46 DIAGNOSIS COM Based on Clinical laboratory and imaging studies

47 CLINICAL EVALUATION COM Skin and soft tissue integrity Tenderness Bone stability Neurovascular status of limb Presence of sinus

48 LABORATORY COM Erythrocyte sedimentation rate C reactive protein WBC count only elevated in 35% Biopsy for histological and microbiological evaluation Staphyloccocus species Anaerobes and gram negative bacilli

49 ORGANISMS IN COM Girasi, 1981 found that the commonest organisms found at the orthopaedic unit at Kenyatta national hospital, then in kabete was staphylococcus aureus which was resistant to penicillin and ampicillin

50 IMAGING STUDIES IN COM Plain X rays Cortical destruction Periosteal reaction Sequestra Sinography

51 SINOGRAPHY

52 IMAGING - Isotopic bone scanning more useful in acute than in chronic osteomyelitis Gallium scans increased uptake in areas where leucocytes and bacteria accumulate. Normal scan excludes osteomyelitis

53 COM IMAGING CT Scan Identifying sequestra Definition of cortical bone and surrounding soft tissues

54 COM IMAGING MRI Shows margins of bone and soft tissue oedema Evaluate recurrence of infection after 1 year Rim sign- well defined rim of high signal intensity surrounding the focus of active disease Sinus tracks and cellulitis

55 TREATMENT OF COM Surgical treatment mainstay Sequestrectomy Resection of scarred and infected bone and soft tissue Radical debridement Resection margins >5mm

56 SURGICAL TREATMENT OF COM Adequate debridement leaves a dead space that needs to be managed to avoid recurrence, or bony instability Skin grafts, Muscle and myocutaneous flaps Free bone transfer Papineau technique Hyperbaric oxygen therapy Vacuum dressing

57 TREATMENT OF COM Antibiotic duration is controversial 6 week is the traditional duration 1 week IV, 6 weeks of oral therapy Antibiotic polymethyl methacrylate (PMMA) beads as a temporary filler of dead space Biodegradable antibiotic delivery system

58 RESECTION OR EXCISION FOR COM Resection of a segment of affected bone may be necessary to control infection With techniques of bone and soft tissue transport, massive resections can be performed and reconstructed without significant disability.

59 RESECTION OR EXCISION FOR COM

60 AMPUTATION FOR OSTEOMYELITIS Amputation indications include Arterial insufficiency Major nerve paralysis Non functional limb-stiffness, contracture Malignant change Prevalence of maliganacy arising from COM reported as 0.2 to 1.6% of cases. Most are squamous cell carcinoma, also reticulum cell carcinoma,fibrosarcoma

61 SCLEROSING OSTEOMYELITIS OF GARRE Bone is thickened and distended, but abscesses and sequestra are absent. Cause unknown Thought to caused by a low grade, possibly anaerobic bacterium

62 SCLEROSING OSTEOMYELITIS OF GARRE

63 REFERENCES Canale Terry and Beaty James (2007) Campbell s Operative Orthopaedics, Philadelphia, Mosby Ben Mbonye-Girasi (1981) Mode of Presentation and End results of Management of Haematogenous Osteomyelitis at the Orthopaedic Unit Kenyatta National Hospital over a Five Year Period. Nairobi : unpublished masters in medicine project, School of Medicine, University of Nairobi Issac K Ngetich (2002) A Study of Haematogenous Osteomyelitis in Children in Kenyatta National Hospital Kenya. Nairobi : unpublished masters in medicine project, School of Medicine, University of Nairobi Lewis R P, Sutter V L and Finegold S M (1978) Bone Infections Involving Anaerobic Bacteria. Baltimore pub med PMID