ADULT
ADULT
ORTHOPAEDIC INFECTIONS
1.1 Osteomyelitis
1.1.1 Acute Osteomyelitis
Common organisms:
Staphylococcus aureus (80%)
Group A Streptococcus pyogenes
Rarely gram negative bacilli
Preferred
Empirical coverage:
Cloxacillin 2g IV q6h
To tailor antibiotics according to definitive cultures.
Alternative
Antibiotic allergy:
Cefazolin 2g IV q6-8h
Comments
Duration:
Initial IV therapy for 2-4 weeks followed by oral therapy. Minimum duration: 6 weeks. Modify according to clinical response.
Antibiotic therapy tailored to tissue/bone C&S result.
4 weeks of IV antibiotics is required for Staphylococcus aureus osteomyelitis associated with bacteraemia.
Conversion from IV to PO therapy with good bioavailability can be done after minimum 2 weeks of IV antibiotics provided:
Patient has no significant comorbidity
Uncomplicated infection with source control
Clinical response seen
Patient able to tolerate orally
Suitable oral antibiotics with good oral bioavailability & proven sensitivity to causative organism
A shorter duration of antibiotics can be considered if the osteomyelitis is fully resected (E.g.: amputation with a clear margin):
No surrounding soft tissue infection: 5 days.
Evidence of soft tissue infection: 10-14 days.
Refer to Appendix 3 for antibiotic allergy.
1.1.2 Chronic Osteomyelitis
Commonest organism: Staphylococcus aureus
Definition:
Relapsing infection despite adequate duration of appropriate antibiotic
Chronic pain/swelling/bone tenderness associated with tissue necrosis, increased drainage or persistent sinus tracts
Presence of bone destruction and presence of sequestra on imaging
Empirical treatment before taking adequate cultures is not recommended. Choice of antibiotic depends on C&S result from tissue/bone as superficial swab culture NOT reliable.
Thorough surgical debridement required (removal of dead bone / orthopaedic hardware).
Treat until inflammatory parameters are normal.
Duration: 6 weeks to 3 months.
A shorter duration of antibiotics can be considered if the osteomyelitis is fully resected (E.g.: amputation with a clear margin):
No surrounding soft tissue infection: 5 days
Evidence of soft tissue infection: 10-14 days
1.1.3 Vertebral Osteomyelitis
This includes pyogenic spine infections, both acute and chronic.
Common organisms:
Staphylococcus aureus (main),
Brucella,
Salmonella,
Gram negative Bacilli
Preferred
Empirical therapy should be withheld unless the patient is septic or in patients with neurologic compromise.
CT-guided needle biopsy & aspiration should be done & specimen sent for C&S.
Cloxacillin 2g IV q4h
Alternative
Cefazolin 2g IV q6-8h
Comments
Empiric gram negative (3rd or 4th generation cephalosporin) should be covered if patient had:
Recent spinal hardware inserted or surgery
Intra-abdominal infections
Co-existing or synchronous genitourinary infection
Immunocompromised
Antibiotic therapy tailored to tissue/bone C&S result.
Conversion from IV to oral therapy with good bioavailability can be done after minimum 2 weeks of IV antibiotics.
Duration:
Minimum 6 weeks.
Minimum 8 weeks if undrained paravertebral abscess(es) and/or infection due to drug-resistant organisms.
Up to 12 weeks if extensive bone destruction or infection due to Brucella sp.
Refer to brucellosis under Tropical Infections section for infection due to Brucella sp.
1.1.4 Implant-associated vertebral osteomyelitis
Early onset (within 30 days of implant insertion): Staphylococcus aureus, Beta-hemolytic streptococci, Gram-negative bacilli
Late onset (>30 days of implant insertion): Staphylococcus aureus, CoNS, Corynebacterium spp., P. acnes
Empirical treatment before taking adequate cultures is not recommended. Antibiotic selection is based on bone C&S.
Duration: Minimum 12 week, final treatment duration depends on hardware retention/removal.
1.2 Septic Arthritis
Common organisms: Staphylococcus/ Streptococcus
Preferred
Cloxacillin 2g IV q4-6h
Alternative
Antibiotic allergy:
Cefazolin 2g IV q6-8h
OR
Clindamycin 600mg IV q6h, followed by oral therapy (same dose)
OR
*Vancomycin 15-20mg/kg (actual body weight) IV q8-12h; not to exceed 2g/dose
Comments
Drainage, debridement and washout of infected joints is important to limit further damage.
Duration:
Parenteral therapy 2-4 weeks, then oral therapy to complete total 4-6 weeks.
A shorter duration of therapy is possible in immunocompetent patients who have had adequate surgical drainage.
Refer to Appendix 3 for antibiotic allergy.
*Vancomycin: If suspected/confirmed MRSA. Consider loading dose 25-30mg/kg for critically ill or septic patients to achieve faster steady state.
Empirical therapy wherever possible should be directed by the result of the gram stain of the joint aspirate.
To consider gonococcal arthritis In a sexually active patient. Refer to the Sexually Transmitted Infections section.
1.3 Prosthetic Joint Infection & Implant Related Infection after Fracture Fixation
1.3.1 Prosthetic Joint Infections
Early onset (<3 months after surgery): Staphylococcus aureus, Gram negative Bacilli
Delayed onset (from 3 to 12 months after surgery): Less virulent organism; CoNS/Enterococcus/anaerobes
Late onset (>12 months after surgery): Staphylococcus aureus, Enterobacteriaceae, B hemolytic Streptococcus, Anaerobes
Empirical therapy is not recommended.
Treatment concepts:
Treatment is based on culture and sensitivity.
In staphylococcal infection, rifampicin should be added in combination with at least one other anti-staphylococcal agent, several days after surgical debridement when implant is retained/exchanged following surgery.
Treatment strategy and duration of treatment depends on surgical strategy.
1.3.2 Definitive Prosthetic Joint Infection treatment- Methicillin-sensitive Staphylococcus aureus (MSSA)
Preferred
Initial treatment:
Cloxacillin 2g IV q4-6h
OR
Cefazolin 2g IV q6-8h
PLUS
Rifampicin 300mg PO q12h OR 600mg PO q24h
Alternative
--
Comments
Duration:
2-6 weeks for IV therapy (according to treatment strategy).
Followed by an oral combination therapy according to susceptibility. Rifampicin should be included if the implant is in situ.
1.3.3 Definitive Prosthetic Joint Infection treatment- Methicillin-resistant Staphylococcus aureus (MRSA)
Preferred
Initial treatment:
*Vancomycin 15-20mg/kg (actual body weight) IV q8-12h; not to exceed 2g/dose
PLUS
Rifampicin 300mg PO q12h OR 600mg PO q24h
Alternative
--
Comments
Duration:
2-6 weeks for IV therapy (according to treatment strategy)
Followed by an oral combination therapy according to susceptibility. Rifampicin should be included if the implant is in situ.
*Refer to Appendix 1 for vancomycin loading dose.
1.3.4 Fracture fixation device infection
Fracture fixation devices include plates, screws, intramedullary nails, rods, and pins from external fixation devices.
Early onset (less than 2 weeks): Highly virulent organisms (Staphylococcus aureus or gram-negative bacilli)
Delayed onset (2–10 weeks): Less virulent organisms (Staphylococcus epidermidis or Cutibacterium acnes)
Late onset (more than 10 weeks): Low virulence organisms (Staphylococcus epidermidis)
Preferred
Intraoperative tissue culture should be taken to guide antibiotic regimen.
Empirical therapy is not recommended unless patient is septic.
Ampicillin/sulbactam 3g IV q6h
Alternative
--
Comments
Treatment concepts:
Treatment is based on culture and sensitivity.
In staphylococcal infection, rifampicin should be added in combination with at least one other anti-staphylococcal agent, several days after surgical debridement when implant is retained/exchanged following surgery.
Treatment strategy and duration of treatment depends on surgical strategy.
2.1 Diabetic Foot Infections
Antibiotics should not be used unless there are local or systemic symptoms of infection. Local treatment including surgical debridement is important. Antibiotic selection should be based on the most recent culture and sensitivity report.
2.1.1 Mild Infections
At least 2 of these items are present:
Local swelling / induration
Erythema > 0.5 but < 2cm around the wound
Local tenderness / pain
Local increased warmth
Purulent discharge
And no other cause of an inflammatory response of the skin (E.g.: trauma, gout, thrombosis).
Preferred
Cloxacillin 500mg PO q6h
OR
Cephalexin 1g PO q12h
Alternative
Amoxicillin/clavulanate 625mg PO q8h
OR
Ampicillin/sulbactam 375-750mg PO q12h
Comments
Duration: 1-2 weeks*
*10 days following surgical debridement
2.1.2 Moderate to severe diabetic foot infections
Moderate infections
Infection with no systemic manifestations and involving:
Erythema extending ≥ 2cm from the wound margin, and/or
Tissue deeper than skin and subcutaneous tissues (e.g.: tendon, muscle, joint, and bone)
Severe infections
Any foot infection with associated systemic manifestations (≥ 2 SIRS)
Preferred
Amoxicillin/clavulanate 1.2g IV q8h
OR
Ampicillin/sulbactam 3g IV q6h
If pseudomonas is suspected:
** Piperacillin/tazobactam 4.5g IV q6-8h
OR
Cefepime 2g IV q8h
If MRSA is suspected:
***Vancomycin 15-20mg/kg q8-12h; not to exceed 2g/dose
Alternative
Cefuroxime 1.5g IV q8h
PLUS
*Metronidazole 500mg IV q8h
Comments
Duration for skin & soft tissues involvement:
Total duration 2-4 weeks
Duration for bone/joint involvement:
Resected: total duration 2-5 days
Debrided for infected soft tissue: total duration 1-2 weeks
Positive culture or histology of bone margins after bone resection: total duration 3 weeks
No surgery or dead bone: total duration 6 weeks
IV to PO switch can be considered if adequate source control is performed.
*Metronidazole: In ischemia limb / necrosis / gas forming.
**Piperacillin/tazobactam: if given as q8h, to be given as extended infusion (over 3-4 hours)
***Refer to Appendix 1 for vancomycin loading dose.
Refer to Appendix 3 for antibiotic allergy.
Surgical debridement is URGENT for severe infections. Antibiotics should be streamlined based on intraoperative culture and sensitivity.
2.2 Necrotizing Fasciitis
Necrotizing fasciitis is a rapidly progressing, life-threatening soft tissue infection with extensive fascial necrosis & relative sparing of underlying muscle caused by a toxin-producing bacterium. Presentation is acute (over hours); rarely, subacute (over days), and is followed by rapid progression to extensive destruction, which can lead to systemic toxicity, limb loss, and/or death.
The rapidness of erythema progression (~1-2 hours) helps differentiate necrotizing fasciitis from cellulitis and indicates the need for urgent surgical intervention.
Immediate aggressive surgical debridement is the primary treatment modality. Repeated surgical debridement for source control is normally necessary.
Etiology may be polymicrobial (mixed aerobic-anaerobic microbes) or monomicrobial (most commonly Group A streptococcus).
Empirical therapy should be broad and antibiotics should be streamlined based on intraoperative culture & sensitivity.
Necrotizing fasciitis commonly involves the extremities. Refer to the respective organ/system sections for other presentations i.e. necrotizing fasciitis of the perineum (Fournier gangrene), head and neck region, and neonatal infection.
2.2.1 Type 1: Polymicrobial infection
Risk factor: older age group, immunocompromised or chronic diseases. E.g.: diabetes.
Organisms:
Anaerobes (E.g.: Bacteroides, Clostridium or Peptostreptococcus)
Facultative anaerobic
Enterobacteriaceae (E.g.: Escherichia coli, Enterobacter, Klebsiella, Proteus)
Facultative anaerobic streptococci (other than Group A streptococcus [GAS])
Obligate aerobes (E.g.: Pseudomonas aeruginosa)
Preferred
*Piperacillin/tazobactam 4.5g IV q6-8h
MAY ADD
**Clindamycin 600-900mg IV q8h
Alternative
Meropenem 1g IV q8h
OR
Imipenem 1g IV q6-8h
MAY ADD
**Clindamycin 600-900mg IV q8h
Comments
Duration:
There is a lack of any convincing evidence regarding the ideal duration of antibiotic therapy, which varies between 7 and 14 days. In general, antibiotics should be continued until no further debridement is needed and the patient’s hemodynamic status has normalized.
*Piperacillin/tazobactam: if given as q8h, to be given as extended infusion (over 3-4 hours)
**Clindamycin should be started empirically if there is risk of Group A Streptococcus or presence of gas crepitus.
Duration: 3-5 days. To stop clindamycin if there is no evidence of Group A Streptococcus.
2.2.2 Type 2: Monomicrobial infection
Group A Streptococcus (most common)
Preferred
Benzylpenicillin 2-4MU IV q4h
PLUS
*Clindamycin 600-900mg IV q8h
Alternative
--
Comments
Duration:
There is a lack of any convincing evidence regarding the ideal duration of antibiotic therapy, which varies between 7 and 14 days. In general, antibiotics should be continued until no further debridement is needed and the patient’s hemodynamic status has normalized.
*If confirmed Group A Streptococcus: Clindamycin & penicillin combination therapy is given until patients are clinically and hemodynamically stable for at least 48 to 72 hours; followed by penicillin monotherapy thereafter.
2.2.3 Water Related Wound Infection
Common organisms:
Vibrio vulnificus (fresh water),
Aeromonas hydrophilia (ocean / brackish water)
Preferred
Ceftriaxone 2g IV q24h
PLUS
Doxycycline 100mg PO q12h
Alternative
Ciprofloxacin 400mg IV q8h
Comments
--
2.3 Myonecrosis / Gas Gangrene
Common organisms: Clostridium sp (80-95%)
Preferred
Mild:
Benzylpenicillin 4MU IV q4h
PLUS
Clindamycin 600-900mg IV q8h
Moderate to severe:
*Piperacillin/tazobactam 4.5g IV q6-8h
PLUS
Clindamycin 600-900mg IV q8h
Alternative
--
Comments
Aggressive surgical debridement is necessary to remove all necrotic tissue.
Duration: total 10-28 days
Refer to Urinary Tract Infection and Gastrointestinal Infection sections for other gas forming infections (E.g.: emphysematous pyelonephritis and emphysematous cholecystitis)
*Piperacillin/tazobactam: if given as q8h, to be given as extended infusion (over 3-4 hours).
References:
Katie A. et.al. Clinical Management of Septic Arthritis. Curr Rheumatol Rep (2013) 15:332
Mathews CJ et. al. Bacterial septic arthritis in adults. Lancet 2010 375(9717): 846
Berbari et al .IDSA 2015: Clinical Practice Guidelines for the Diagnosis and Treatment of Native Vertebral Osteomyelitis in Adults
George Varghese et al. Investigating and managing pyrexia of unknown origin in adults. BMJ 2010;341:c5470
Michales P et.al. Chronic osteomyelitis: what the surgeon needs to know. EFORT Open Rev 2016
Uptodate: Vertebral osteomyelitis and discitis in adults. Aug 16, 2022
Werner Zimmerli: Bone and Joint Infections from Microbiology to Diagnostics and Treatment. Wiley Blackwell 2015
Clinical Practice Guidelines by the Infectious Diseases Society of America: Diagnosis and Management of Prosthetic Joint Infection 2012
Uptodate: Prosthetic Joint Infection-Treatment. Oct 12, 2022.
Pocket Guide to Diagnosis and Treatment of implant-associated infections after fracture fixation. Version 2: 1. October 2017
Steinmetz, S.et.al. (2019). Infection after fracture fixation. EFORT Open Reviews, 4(7), 468-475. Retrieved Jul 21, 2023, from https://doi.org/10.1302/2058-5241.4.180093
Zimmerli, W. (1998). Role of Rifampin for Treatment of Orthopedic Implant–Related Staphylococcal Infections A Randomized Controlled Trial. JAMA, 279(19), 1537. doi:10.1001/jama.279.19.1537
CPG 2018: Management of Diabetic Foot 2nd edition. Published by Malaysian Health Technology Assessment Section (MaHTAS).
Guidelines on the diagnosis and treatment of foot infection in persons with diabetes IWGDF/IDSA 2023
Peter EO et.al. Infections of the musculoskeletal system Basic principles, prevention, diagnosis and treatment. 1st electronic edition in English 2016
Uptodate: Necrotizing soft tissue infections. Oct 7, 2022.
Practice Guidelines for the Diagnosis and Management of Skin and Soft Tissue Infections: 2014 Update by the Infectious Diseases Society of America
Uptodate: clostridial myonecrosis