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2,6-Dimethoxyphenol Penicillin in Infants and ChildrenPreliminary Studies
PAUL A. DAY, M.D.;
WINIFRED OSBORN;
HOWARD L. WEINBERGER, M.D.;
WILLIAM MESIBOV;
HENRY ROBIDOUX;
PAUL F. WEHRLE, M.D.
Am J Dis Child. 1961;102(6):785-792.
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The control and treatment of disease due to staphylococci still present a serious medical problem in spite of the availability of many effective antibacterial agents. This is particularly true in the newborn nursery. With improved hygiene, better regulation of nurseries, and the use of potent antibiotics, staphylococcal infection still occurs with considerable frequency. Difficulties in the control of this infection lie both in the facility with which the organism is transmitted as well as in the variable antibiotic resistance patterns observed with hospital strains. Numerous studies and reviews of the epidemiology and bacteriology of nursery-acquired staphylococcal infections have appeared in the literature.1-12
A new derivative of penicillanic acid, 2,6-dimethoxyphenyl penicillin, appears to inhibit the growth, in vitro, of staphylococci resistant to penicillin G.13 Since this isomer is well absorbed on parenteral administration and has been shown to be nontoxic in animals, it appears to offer considerable promise in
. . . [Full Text PDF of this Article]
Author Affiliations
SYRACUSE, N.Y.
Paul A. Day, M.D., Department of Microbiology, State University of New York, Upstate Medical Center, 766 Irving Ave., Syracuse 10, N.Y.; From the Departments of Pediatrics and Microbiology, State University of New York Upstate Medical Center.
Footnotes
Submitted for publication Feb. 17, 1961.
Present address of Dr. Wehrle is Communicable Disease Division, Los Angeles County General Hospital, 1200 N. State Street, Los Angeles 33, Calif.
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