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Biomedical subjects

B Sugarman

Publications and source records attributed to B Sugarman.

56 records · Page 4Linked to original sources

Treatment failures secondary to in vivo development of drug resistance by microorganisms.

In two patients development of resistance to antibiotics by initially sensitive infecting organisms was associated with relapse or persistence of active infection. The first patient developed Staphylococcus epidermidis resistant to chloramphenicol during therapy with this agent for an infection that followed a cerebrospinal fluid shunt, and the second patient developed bacteremia due to ampicillin-resistant Salmonella during therapy with ampicillin. Treatment failure resulting from in vivo development of resistance to antimicrobial agents has been described for most of the major classes of antiinfective drugs and for numerous microorganisms. Although in many of these instances reinfection with a resistant organism cannot be excluded, there are many examples of apparent mutation or initial infection with both sensitive and resistant bacterial populations that is followed by selective multiplication of the resistant population or acquisition of resistance by an initially sensitive infecting organism. This phenomenon can be a cause of treatment failure and has appeared in patients in whom, by available tests, drug levels were found adequate. Isolation days after the institution of antimicrobial therapy of what appears to be the same organism as was initially recovered should prompt repeated sensitivity tests, at least to the agents being administered, if the patient's clinical course has not been one of satisfactory improvement.

Adult↗

Zinc and infection.

Zinc is necessary for the normal functioning of all living systems. In microbes and mammals vital biological roles of zinc include the presence of this metal in metalloenzymes and membrane stabilization. In addition, zinc may bind nonspecifically to sulfhydryl, histidine, or other moieties on membranes, enzymes, or other proteins and alter their activity. Serum levels of zinc decrease sharply in many infections. Levels slightly below normal seem to be associated with optimal phagocytic function, and low concentrations of zinc may decrease microbial virulence. Brief decreases in serum levels appear to have no detrimental effect on host immunity and may act as a protective measure by decreasing the ability of indigenous or infecting microbes to thrive. However, prolonged zinc deficiency in mammals is associated with depressed T-cell function but near normal B-cell function. More work is needed for better understanding of zinc-related biochemistry and for determining the relationship between zinc status and susceptibility to infection in mammals.

Animals↗