Abstract
A review is given of the selection and rationale of optimal treatment regimens for patients with sexually transmitted pathogens, e.g. in cases of gonorrhea, chlamydial infections, chancroid, syphilis, pelvic inflammatory diseases and ophthalmia neonatorum. The scientific basis for the selection of a beta-lactam agent is discussed, including dose, MIC, the critical serum level and maintenance interval, and the duration of therapy. Except in the case of penicillinase-producingNeiserria gonorrhoeae, penicillin remained until recently the most effective agent available against many sexually transmitted diseases. However, ceftriaxone, a new third-generation cephalosporin, has been shown to have a long half-life (8 h) and excellent in vitro efficacy againstNeiserria gonorrhoeae (including penicillinase-producing strains) andHaemophilis ducreyi. In view of its exceptional clinical efficacy against both gonorrhea and chancroid, clinical studies of its efficacy against other sexually transmitted diseases appear warranted.
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Eagle, H., Fleischman, R., Musselman, A. D.: The effective concentrations of penicillin in vitro and in vivo for streptococci, pneumococci andTreponema pallidum. Journal of Bacteriology 1950, 59: 625–643.
Eagle, H., Fleischman, R., Musselman, A. D.: Effect of schedule of administration on the therapeutic efficacy of penicillin. American Journal of Medicine 1950, 9: 280–299.
Jaffe, H. W., Shroeter, A. L., Reynolds, G. H., Zaidi, A. A., Martin, J. E., Thayer, J. D.: Pharmacokinetic determinants of penicillin cure of gonococcal urethritis. Antimicrobial Agents and Chemotherapy 1979, 15: 587–591.
Adams, H. G., Turck, M., Holmes, K. K.: Comparison of aqueous sodium penicillin G in lidocaine and aqueous procaine penicillin G for the treatment of gonorrhea. In: Danielsson, D., Jahlin, L., Mardh, P. A. (ed.): Genital infections and their complications. Almquist and Wiksell International, Stockholm, 1975, p. 279–284.
Jaffe, H. W., Biddle, J. W., Thornsberry, C., Johnson, R. E., Kaufman, R. E., Reynolds, G. H., Wiesner, P. J., and the Cooperative Study Group: National gonorrhea therapy monitoring study. In vitro antibiotic susceptibility and its correlation with treatment results. New England Journal of Medicine 1976, 294: 5–9.
Leigh, D. A., LeFranc, J., Turnbell, A. R.: Sensitivity to penicillin ofNeisseria gonorrhoeas. Relationship to the results of treatment. British Journal of Venereal Diseases 1969, 45: 151–153.
Wiesner, P. J., Handsfield, H. H., Holmes, K. K.: Low antibiotic resistance of gonococci causing disseminated infection. New England Journal of Medicine 1973, 288: 1221–1222.
Blankeship, R. M., Holmes, R. K., Sanford, J. P.: Treatment of disseminated gonococcal infection. New England Journal of Medicine 1974, 290: 267–269.
Johnson, D. W., Kvale, P. A., Virgilio, L. A., Stewart, S. D., Halverson, C. W., Holmes, K. K.: Single-dose antibiotic treatment of asymptomatic gonorrhea in hospitalized women. New England Journal of Medicine 1970, 283: 1–6.
Karney, W. W., Turck, M., Holmes, K. K.: Single-dose oral therapy for uncomplicated gonorrhea: comparison of amoxicillin and ampicillin given with and without probenecid. Journal of Infectious Diseases 1974, 129 (Supplement): S250-S253.
Barbhaiya, R., Thin, R. N., Turner, P., Wadsworth, J.: Clinical pharmacological studies of amoxycillin: effect of probenecid. British Journal of Venereal Diseases 1979, 55: 211–213.
Karney, W. W., Turck, M., Holmes, K. K.: Cefazolin in the treatment of gonorrhea. Journal of Infectious Diseases 1973, 128 (Supplement): S399-S304.
Nelson, M.: Cefazolin in the treatment of uncomplicated gonorrhea in men. Journal of Infectious Diseases 1973, 128 (Supplement): S404-S406.
Kirby, W. M., Regamey, C.: Pharmacokinetics of cefazolin compared with four other cephalosporins. Journal of Infectious Diseases 1973, 128 (Supplement): S341-S346.
Duncan, C.: Treatment of gonorrhea with cefazolin plus probenicid. Journal of Infectious Diseases 1974, 130: 398–401.
Ng, W. S., Chau, P. Y., Arnold, K.: In vitro susceptibility ofHaemophilus influenza andNeisseria gonorrhoeae to Ro 13-9904 in comparison with otherβ-lactam antibiotics. Antimicrobial Agents and Chemotherapy 1978, 223: 477–478.
Sonneville, K. S., Albert, K. S., Skeggs, H., Gentner, H., Kovan, R. C., Martin, C. M.: Effect of lidocaine on the absorption, disposition, and tolerance of intramuscularly administered cefoxitin. European Journal of Clinical Pharmacology 1977, 12: 273–279.
Shrogie, J. J., Rogers, J. D., Yeh, K. C., Davies, R. D., Holmes, G. E., Skeggs, H., Martin, C. M.: Pharmacokinetics and comparative pharmacology of cefoxitin and cephalosporins. Reviews of Infectious Diseases 1979, 1: 90–97.
Seigel, M. S., Thompson, S. E., Perine, P. L., Brown, S. T., Reynolds, G., Thornsberry, C.: Treatment of uncomplicated gonococcal urethritis with cefoxitin: comparison with penicillin. Review of Infectious Diseases 1979, 1: 183–187.
Berg, S. W., Kilpatrick, M. E., Harrison, W. O., McCutchan, J. A.: Cefoxitin as a single-dose treatment for urethritis caused by penicillinase producingNeisseria gonorrhoeae. New England Journal of Medicine 1979, 301: 509–511.
Foord, R. D.: Cefuroxime: human pharmacokinetics. Antimicrobial Agents and Chemotherapy 1976, 9: 741–747.
Fowler, W., Rahim, G., Brown, J. D.: Clinical experience in the use of cefuroxime in gonorrhea. British Journal of Venereal Diseases 1978, 54: 400–402.
Nayyar, K. C., Michel, M. F., Stolz, E.: Antibiotic sensitivities of gonococci isolated in Rotterdam and results of treatment with cefuroxime. British Journal of Venereal Diseases 1980, 56: 244–251.
DeKoning, G. A. J., Tio, D., Van der Hoek, J. A. R., Van Klingeren, B.: Single 1 g dose of cefotaxime in the treatment of infections due to penicillmase-producing strains ofNeisseria gonorrhoeae. British Journal of Venereal Diseases 1983, 59: 100–102.
Handsfield, H. H., Holmes, K. K.: Treatment of uncomplicated gonorrhea with cefotaxime. Sexually Transmitted Diseases 1981, 8: 187–191.
Simpson, M. L., Khan, M. Y., Siddiqui, Y., Gruninger, R. P., Wigren, D. I.: Treatment of gonorrhea: comparison of cefotaxime and penicillin. Antimicrobial Agents and Chemotherapy 1981, 19: 798–800.
Patel, I. H., Weinfled, R. E., Konikoff, J., Parsonnet, M.: Pharmacokinetics and tolerance of ceftriaxone in humans after single dose intramuscular administration in water and lidocaine diluents. Antimicrobial Agents and Chemotherapy 1982, 21: 957–962.
Handsfield, H. H., Murphy, V. L., Holmes, K. K.: Dose ranging study of ceftriaxome for uncomplicated gonorrhea in men. Antimicrobial Agents and Chemotherapy 1981, 20: 839–840.
Zajdowic, T. R., Sanches, P. L., Berg, S. W., Kerbs, S. B. J., Newquist, R. L., Harrison, W. O.: Comparison of ceftriaxone with cefoxitin in the treatment of penicillin-resistant gonococcal urethritis. British Journal of Venereal Diseases 1983, 59: 176–178.
Shacter, J.: Chlamydia infections. New England Journal of Medicine 1978, 298: 428–435.
Bowie, W. R., Lee, C. K., Alexander, E. R.: Prediction of efficacy of antimicrobial agents in treatment of infections due toChlamydia trachomatis. Journal of Infectious Diseases 1978, 1380: 655–659.
Kramer, M. J., Gordon, F. B.: Ultrastructural analysis of the effects of penicillin and chlortetracycline on the development of genital tract chlamydia. Infection and Immunity 1971, 3: 333.
Harbour, A. G., Amano, K. I., Hackstadt, T., Perry, L., Caldwell, H. D.:Chlamydia trachomatis has penicillin-binding proteins but not detectable muramic acid. Journal of Bacteriology 1982, 151: 420–428.
Hammerschlag, M. R., Gleyzer, A.: In-vitro activity of a group of broad spectrum cephalosporins and otherβ-lactam antibiotics againstChlamydia trachomatis. Antimicrobial Agents and Chemotherapy 1983, 23: 493–494.
Stamm, W. E., Giunen, M. E., Johnson, C., Starcher, T., Holmes, K. K., McCormack, W. M.: Effect of treatment regimens forNeisseria gonorrhoeas on simultaneous infection withChlamydia trachomatis. New England Journal of Medicine 1984, 310: 545–549.
Eichman, A., Weidmann, G., Havas, L.: One dose treatment of acute uncomplicated gonorrhea of male patients with ceftriaxone Rol3-8804, a new parenteral cephalosporin. Chemotherapy 1981, 281S: 62–69.
Bowie, W. R., Alexander, E. R., Holmes, K. K.: Eradication ofChlamydia trachomatis from the urethras of men with nongonococcal urethritis by treatment with amoxicillin. Sexually Transmitted Diseases 1981, 8: 79–81.
Nsanze, H., Fast, M. V., D'Costa, L. J., Tukei, P., Curran, J., Ronald, A.: Genital ulcers in Kenya: clinical and laboratory study. British Journal of Venereal Diseases 1981, 57: 378–381.
Fast, M. V., Nsanze, H., D'Costa, L. J., Karasira, P., Maclean, I., Piot, P., Albritton, W. L., Ronald, A. R.: Antimicrobial therapy of chancroid: an evaluation of five treatment regimens correlated with in-vitro sensitivity. Sexually Transmitted Diseases 1983, 10: 1–6.
Albritton, W. L., Brunton, J. L., Slaney, L., Maclean, L.: Plasmid mediated sulfonamide resistance inHaemophilus ducreyi. Antimicrobial Agents and Chemotherapy 1982, 21: 159–165.
Plummer, F. A., Nsanze, H., D'Costa, L. J., Karasira, P., Maclean, I. W., Ellison, R. H., Ronald, A. R.: Single-dose therapy of chancroid with trimethoprim-sulfametrole. New England Journal of Medicine 1983, 309: 67–71.
Idse, O., Guthe, T., Wilcos, R. R.: Penicillin in the treatment of syphilis. Bulletin World Health Organization 1972, 47: 1–68.
Glicksman, J. M., Short, D. H., Knox, J. M.: Parenteral cephaloridine treatment of patients with early syphilis. Archives of Internal Medicine 1968, 121: 342–344.
Nicolis, G., Loucopoucos, A.: Cephalothin in the treatment of syphilis. British Journal of Venereal Diseases 1974, 50: 270–271.
Acred, P., Grujil, P., Ryan, D. M., Xerri, L., Orsolini, P., Erani, E.: In-vitro activity of cefuroxime againstTreponema pallidum and Neisseria gonorrhoeas. Journal of Antimicrobial Chemotherapy 1980, 6: 407–408.
Johnson, R. C., Bey, R. R., Wolgamot, S. J.: Comparison of the activities of ceftriaxone and penicillin G against experimentally induced syphilis in rabbits. Antimicrobial Agents and Chemotherapy 1982, 21: 984–989.
Sweet, R. L.: Pelvic inflammatory disease: etiology, diagnosis, and treatment. Sexually Transmitted Diseases 1981, 8: 308–348.
Brunham, R. C.: Therapy for acute pelvic inflammatory diseases: a critique of recent treatment trials. American Journal of Obstetrics and Gynecology 1984, 148: 235–240.
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Kunimoto, D., Brunham, R. & Ronald, A. Beta-lactams in sexually transmitted diseases: Rationale for selection and dosing regimens. Eur. J, Clin. Microbiol. 3, 605–611 (1984). https://doi.org/10.1007/BF02013632
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DOI: https://doi.org/10.1007/BF02013632