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  Vol. 137 No. 8, August 1983 TABLE OF CONTENTS
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Ampicillin-Resistant Hemophilus influenzae From Patients With Cystic Fibrosis

VINCENT P. McCARTHY, MD; TERESA C. WU, PHD; VAN S. HUBBARD, MD, PHD

Am J Dis Child. 1983;137(8):802-803.

Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings.

Since 1973, ampicillin-resistant isolates of nontypeable Hemophilus influenzae have increased in prevalence and clinical significance. Previous reports, however, have primarily been restricted to otitis media.1,2Hemophilus influenzae frequently colonizes the respiratory tract of patients with cystic fibrosis and chronic bronchitis, and ampicillin-resistant strains of H influenzae have been isolated from patients with chronic bronchitis.3,4 As bronchopulmonary infection is the most common cause of morbidity and mortality in patients with cystic fibrosis,5 the occurrence of drug-resistant potential pathogens in this patient population is of importance. We retrospectively review the incidence of ampicillin-resistant strains of H influenzae and other Hemophilus species isolated from the sputum of patients with cystic fibrosis at the National Institutes of Health (NIH), Bethesda, Md, from January 1977 to June 1981.

Methods and Materials.—All results were retrieved by computer, using the Clinical Information Utility System at the Clinical Center of the NIH.

Sputum was . . . [Full Text PDF of this Article]


Author Affiliations

National Institutes of Arthritis, Diabetes, Digestive and Kidney Disease; National Institutes of Health; National Institutes of Arthritis, Diabetes, Digestive and Kidney Disease Bethesda, Md



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