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Septic arthritis of the hip, if untreated, can lead to significant joint destruction and disability or systemic illness.
Early diagnosis and treatment are important for optimizing outcomes.
Clinical history, physical examination, and joint aspiration identify most cases.
Advanced imaging techniques (magnetic resonance imaging [MRI], nuclear medicine) may assist in the assessment of early or subclinical infection.
Multiple surgical options—including arthroscopy, arthrotomy, arthroplasty, and arthrodesis—may be beneficial in treatment.
Septic arthritis is an uncommon, clinically significant condition that can rapidly produce hip joint destruction and physical impairment. If unrecognized or untreated, a septic joint can result in significant localized consequences, including chondrolysis, osteomyelitis, osteonecrosis, and leg length discrepancy ( Fig. 36.1 ). Severe systemic complications, including sepsis and death, may occur and have been noted with increased frequency in association with advanced age. Early diagnosis and initiation of surgical intervention remain essential components of successful treatment. Although septic arthritis occurs most commonly in children or in adults with prosthetic joint replacements, it remains a significant diagnostic consideration in evaluating other adult patients presenting with hip pain.
The most common pathway for entry of infection into the nonreplaced adult hip joint is a hematogenous source. Bacteria from the urinary tract, lungs, skin, or other distant sites can enter the hip joint through inflamed or diseased synovial tissue. Although antegrade flow through the arterial system most likely contributes to most cases, the proximity of the hip to the Batson plexus provides the potential for retrograde venous introduction of bacteria from pelvic floor organs.
Direct introduction of bacteria into the hip joint can also occur through a variety of diagnostic and therapeutic procedures. Although direct joint inoculation historically has contributed to a small percentage of cases, increased use of arthrocentesis, arthroscopy, and open surgical approaches to treat nonarthritic and prearthritic hip conditions may increase hip joint infection rates. Repeated corticosteroid injections to treat hip osteoarthritis have been associated with an increased prosthetic joint infection risk following total hip arthroplasty.
Regional extension of infection from the lumbar spine, genitourinary structures, and lower gastrointestinal tract can also cause hip joint infection. This may occur by direct communication or by extension of infection along the iliopsoas tendon.
Conditions that result in increased venous or arterial perfusion, capillary permeability, or synovial tissue inflammation elevate the potential for bacteria to enter into the hip ( Box 36.1 ). Impaired immune system surveillance—caused by host factors, disease, or pharmacologic immunosuppression—further contributes to an individual's susceptibility for joint sepsis ( Box 36.2 ).
Osteoarthritis
Posttraumatic arthritis
Inflammatory arthropathy
Rheumatoid arthritis
Spondyloarthropathy
Crystalline arthropathy
Periarticular trauma
Osteonecrosis
Sickle cell disease
Charcot arthropathy
Hemophilia
Diabetes mellitus
Systemic lupus erythematosus
Connective tissue disease
Chronic alcoholism
Cirrhosis
Renal failure
Malignancy
Human immunodeficiency virus (HIV)
Radiation therapy
Immunosuppression
Organ transplant
Inflammatory arthropathy
Malnutrition
Advanced age
The most common infecting organisms are similar to those encountered with other musculoskeletal infections. Staphylococcus aureus is the most frequently reported organism resulting in hip infection, accounting for between 30% and 60% of cases. Group A streptococcal bacteria are the second most commonly identified, and an increasing number of infections have been reported with a variety of gram-negative and anaerobic organisms ( Box 36.3 ). Recent trends indicate an increasing incidence of community-acquired methicillin-resistant strains of S. aureus (MRSA) in Western cultures. Among patients with osteonecrosis or sickle cell disease, salmonella has been reported as an organism with a predisposition for the hip at a higher incidence than nonsalmonella infection and may be associated with a chronic carrier state within the necrotic bone in susceptible individuals.
Staphylococcus aureus (MSSA/MRSA)
Staphylococcus epidermidis (coagulase negative)
Streptococcus
Group A
Group B
Pneumococcus
Enterococcus
Escherichia coli
Klebsiella
Proteus
Enterobacter
Pseudomonas
Salmonella
Neisseria
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