Haemophilus influenzae Type b Septic Arthritis in Children: Report of 23 Cases

PEDIATRICS ◽  
1985 ◽  
Vol 75 (2) ◽  
pp. 254-259
Author(s):  
Harley A. Rotbart ◽  
Mary P. Glode

Twenty-three cases of Haemophilus influenzae type b septic arthritis seen over a recent 5-year period are reviewed. The natural history of the disease includes a mean three days of fever and joint symptoms prior to hospitalization, often accompanied or immediately preceded by a viral illness and/or otitis media. Concurrent H influenzae type B meningitis was present in 30% of patients and concurrent osteomyelitis in 22%. Infants remained febrile in the hospital for a mean of 3.6 consecutive days. However, secondary and prolonged fevers were common. Clinical improvement in the joint examination was first seen at a mean of 2.5 days. Characteristic laboratory findings during recovery included a decline in total WBC count, neutrophil count, ESR, and hematocrit, with a concomitant increase in lymphocyte and platelet counts. Outpatient follow-up for a mean duration of 20 months found only two of 21 infants with residual impairment. The time to total healing in the remaining 19 infants, however, varied widely—from nine days to 17 months (mean of 4 months).

PEDIATRICS ◽  
1982 ◽  
Vol 69 (2) ◽  
pp. 230-232
Author(s):  
Paul A. Offit ◽  
Joseph M. Campos ◽  
Stanley A. Plotkin

Haemophilus influenzae type b isolates resistant to ampicillin have been reported with increasing frequency since 1973.1 The mechanism of resistance is usually via production of a plasmid-mediated β-lactamase.2 We report the second clinical isolate of an ampicillin-resistant strain of H influenzae type b with no detectable β-lactamase activity. CASE REPORT A 20-year-old white woman was admitted to The Children's Hospital of Philadelphia with a three-day history of fever to 39 C, cough, tachypnea, and diarrhea. Past medical history was significant for the following: (1) recurrent upper and lower respiratory tract infections first noted at 5 years of age, (2) a selective deficiency of IgG and IgA documented at 8 years of age necessitating monthly immune serum globulin injections, (3) chronic, interstitial pulmonary fibrosis with resultant obstructive and restrictive lung disease, (4) severe cachexia, (5) a chronic, maculopapular facial rash, and (6) recurrent, bilateral serous otitis media and sinusitis.


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