Michael E. Kilpatrick
Stanford University
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Featured researches published by Michael E. Kilpatrick.
The American Journal of the Medical Sciences | 1979
John A. Routenberg; Jules L. Dienstag; William O. Harrison; Michael E. Kilpatrick; Richard R. Hooper; Francis V. Chisari; Robert H. Purcell; Michael F. Fornes
During a 1974 foodborne outbreak of viral hepatitis type A among Navy recruits, we evaluated clinical and laboratory features prospectively in 130affected persons. The ratio of anicteric to icteric persons identified during the outbreak was 1:3.5 but illness was relatively mild in this population of young adults. Infrequently reported in association with type A hepatitis, rash and arthralgias (but not arthritis) were reported by 14 and 10% of affected persons, respectively. Fourteen weeks after onset of acute illness, 8.5% of patients had persistently elevated aminotransferase activities and underwent percutaneous liver biopsy. Morphologic features included piecemeal necrosis, but clinical, biochemical, and histological evidence of disease resolved within five months to one year after the outbreak. Fecal shedding of hepatitis A virus began during the preicteric stage, did not persist beyond the second day of jaundice (even in patients with protracted illness), and was not detected in anicteric patients. Feces and serum obtained during the late incubation period, but not urine, were infectious in chimpanzees. Antibody to hepatitis A virus developed during convalescence, and serum anticomplementary activity was noted during acute illness. Failure of T-lymphocytes to bind sheep erythrocytes and form rosettes was observed, was found to be modulated in several cases by an intrinsic lymphocyte defect and in others by the presence in serum of an extrinsic immunoregulatory serum lipoprotein, “rosette inhibitory factor,” which persisted in patients with slow resolution.
The New England Journal of Medicine | 1979
S. William Berg; Michael E. Kilpatrick; William O. Harrison; J. Allen McCutchan
Gonococci that resist standard penicillin regimens by production of a penicillinase are now well established in certain areas of the world. Because cefoxitin, a semisynthetic cephamycin, resists gonococcal penicillinase in vitro, we compared procaine penicillin G and cefoxitin in treatment of gonorrhea in an area where 40 per cent of isolates produce penicillinase. One hundred and seven men with culture-proved gonococcal urethritis were given a single dose of either procaine penicillin G, 4.8 million U, or cefoxitin, 2 g, intramuscularly. Both groups took 1 g of probenecid orally; cefoxitin was given with lidocaine to reduce pain at the injection site. In men infected with penicillinase-negative gonococci, both cefoxitin and penicillin were highly effective. Penicillin failed in 77 per cent of men with penicillinase-positive strains, whereas cefoxitin was completely successful. Cefoxitin is an effective alternative to spectinomycin for single-session therapy of urethritis caused by penicillinase-producing Neisseria gonorrhoeae.
American Journal of Epidemiology | 1977
Richard R. Hooper; Charles W. Juels; John A. Routenberg; William O. Harrison; Michael E. Kilpatrick; Stephen J. Kendra; Jules L. Dienstag
Military Medicine | 1992
Scott A. Thornton; Stephen F. Wignall; Michael E. Kilpatrick; August L. Bourgeois; Chris H. Gardiner; Roger A. Batchelor; Donald H. Burr; John J. Oprandy; Paul Garst; Kenneth C. Hyams
American Journal of Epidemiology | 1986
Michael E. Kilpatrick; Joel Escamilla
Military Medicine | 1980
Earl A. Edwards; Michael E. Kilpatrick; Dennis R. Hooper
Boletín de la Oficina Sanitaria Panamericana (OSP) | 1986
Michael E. Kilpatrick; Joel Escamilla; A.B Townsend; W Gutiérrez López; E.P Vargas; L Bonilla Castillo
Military Medicine | 1986
Michael E. Kilpatrick; James E. Sheffield
Archive | 1982
Michael E. Kilpatrick; Eric J Mueller; Earl A. Edwards
Military Medicine | 1982
Michael M. Safani; William O. Harrison; Michael E. Kilpatrick; Dennis R. Hooper