[Pharmacokinetic and clinical evaluations of ceftriaxone in perinatal infections in obstetrics and gynecology]. 1988

S Matsuda, and M Suzuki, and T Shimizu, and M Ishikawa, and A Souma, and S Fujimoto, and S Makinoda, and T Chimura, and T Watanabe, and T Oda
Department of Obstetrics and Gynecology, Koto Hospital.

Ceftriaxone (CTRX), an injectable cephem antibiotic agent, was studied for its pharmacokinetic properties and clinical usefulness in perinatal infections in obstetrics and gynecology on a multicenter basis. The study results are summarized below. 1. Following the one-shot intravenous injection of CTRX 1 g to pregnant women before labor, the maternal serum level of CTRX reached a peak at 131.8 micrograms/ml soon after the injection then it began to decrease gradually. T 1/2 was 6.7 hours. The umbilical serum level reached a peak at 16.0 micrograms/ml at 4.9 hours post-dose and decreased gradually with a half-life of 8.1 hours. The umbilical serum level was higher than the maternal serum level at about 12 hours post-dose. The amniotic fluid level reached a peak of 9.6 micrograms/ml at 12.8 hours post-dose. T 1/2 was 15.2 hours. The amniotic fluid level at about 15 hours post-dose or later exceeded the maternal serum level and was almost equal to the umbilical serum level at 24 hours post-dose. 2. Clinical usefulness was evaluated in 79 evaluable cases out of 89 treated for various infections at puerperium or for prophylaxis of infections at cesarean section or premature rupture of membranes (PROM). The efficacy rate was 100% in 7 cases of prenatal infections such as urinary tract infection and 30 cases of postnatal infections such as puerperal intrauterine infections. In 42 cases treated for prophylaxis in cases of cesarean section or PROM, the efficacy rate was 92.9%. Bacteriologically, 29 strains of pathogens were isolated from 26 cases. The disappearance rate of the pathogens was 96.0% as 23 strains were eradicated, 1 strain was substituted and no change was observed in 1 strain with unknown results in 4 strain. Skin rash and itching appeared in 1 patient as an adverse effect (1.1%). There were 10 cases of abnormal clinical laboratory test results such as elevated transaminase level were observed in 7 patients (7.9%). From the results, CTRX was considered to be a useful drug for the perinatal infection in the obstetrics and gynecology fields.

UI MeSH Term Description Entries
D007275 Injections, Intravenous Injections made into a vein for therapeutic or experimental purposes. Intravenous Injections,Injection, Intravenous,Intravenous Injection
D008431 Maternal-Fetal Exchange Exchange of substances between the maternal blood and the fetal blood at the PLACENTA via PLACENTAL CIRCULATION. The placental barrier excludes microbial or viral transmission. Transplacental Exposure,Exchange, Maternal-Fetal,Exposure, Transplacental,Maternal Fetal Exchange
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D008892 Milk The off-white liquid secreted by the mammary glands of humans and other mammals. It contains proteins, sugar, lipids, vitamins, and minerals. Cow Milk,Cow's Milk,Milk, Cow,Milk, Cow's
D011247 Pregnancy The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. Gestation,Pregnancies
D011251 Pregnancy Complications, Infectious The co-occurrence of pregnancy and an INFECTION. The infection may precede or follow FERTILIZATION. Complications, Infectious Pregnancy,Infectious Pregnancy Complications,Maternal Sepsis,Pregnancy, Infectious Complications,Sepsis during Pregnancy,Sepsis in Pregnancy,Infectious Pregnancy Complication,Pregnancy Complication, Infectious,Sepsis in Pregnancies,Sepsis, Maternal
D011292 Premedication Preliminary administration of a drug preceding a diagnostic, therapeutic, or surgical procedure. The commonest types of premedication are antibiotics (ANTIBIOTIC PROPHYLAXIS) and anti-anxiety agents. It does not include PREANESTHETIC MEDICATION. Premedications
D002443 Ceftriaxone A broad-spectrum cephalosporin antibiotic and cefotaxime derivative with a very long half-life and high penetrability to meninges, eyes and inner ears. Benaxona,Cefatriaxone,Cefaxona,Ceftrex,Ceftriaxon,Ceftriaxon Curamed,Ceftriaxon Hexal,Ceftriaxona Andreu,Ceftriaxona LDP Torlan,Ceftriaxone Irex,Ceftriaxone Sodium,Ceftriaxone Sodium, Anhydrous,Ceftriaxone, Disodium Salt,Ceftriaxone, Disodium Salt, Hemiheptahydrate,Lendacin,Longacef,Longaceph,Ro 13-9904,Ro-13-9904,Ro13-9904,Rocefalin,Rocefin,Rocephin,Rocephine,Tacex,Terbac,Anhydrous Ceftriaxone Sodium,Ro 13 9904,Ro 139904,Ro13 9904,Ro139904
D002986 Clinical Trials as Topic Works about pre-planned studies of the safety, efficacy, or optimum dosage schedule (if appropriate) of one or more diagnostic, therapeutic, or prophylactic drugs, devices, or techniques selected according to predetermined criteria of eligibility and observed for predefined evidence of favorable and unfavorable effects. This concept includes clinical trials conducted both in the U.S. and in other countries. Clinical Trial as Topic
D005260 Female Females

Related Publications

S Matsuda, and M Suzuki, and T Shimizu, and M Ishikawa, and A Souma, and S Fujimoto, and S Makinoda, and T Chimura, and T Watanabe, and T Oda
July 1987, The Japanese journal of antibiotics,
S Matsuda, and M Suzuki, and T Shimizu, and M Ishikawa, and A Souma, and S Fujimoto, and S Makinoda, and T Chimura, and T Watanabe, and T Oda
April 1990, The Japanese journal of antibiotics,
S Matsuda, and M Suzuki, and T Shimizu, and M Ishikawa, and A Souma, and S Fujimoto, and S Makinoda, and T Chimura, and T Watanabe, and T Oda
March 1988, The Japanese journal of antibiotics,
S Matsuda, and M Suzuki, and T Shimizu, and M Ishikawa, and A Souma, and S Fujimoto, and S Makinoda, and T Chimura, and T Watanabe, and T Oda
April 1990, The Japanese journal of antibiotics,
S Matsuda, and M Suzuki, and T Shimizu, and M Ishikawa, and A Souma, and S Fujimoto, and S Makinoda, and T Chimura, and T Watanabe, and T Oda
June 1991, The Japanese journal of antibiotics,
S Matsuda, and M Suzuki, and T Shimizu, and M Ishikawa, and A Souma, and S Fujimoto, and S Makinoda, and T Chimura, and T Watanabe, and T Oda
June 1988, The Japanese journal of antibiotics,
S Matsuda, and M Suzuki, and T Shimizu, and M Ishikawa, and A Souma, and S Fujimoto, and S Makinoda, and T Chimura, and T Watanabe, and T Oda
January 1985, The Japanese journal of antibiotics,
S Matsuda, and M Suzuki, and T Shimizu, and M Ishikawa, and A Souma, and S Fujimoto, and S Makinoda, and T Chimura, and T Watanabe, and T Oda
March 1988, The Japanese journal of antibiotics,
S Matsuda, and M Suzuki, and T Shimizu, and M Ishikawa, and A Souma, and S Fujimoto, and S Makinoda, and T Chimura, and T Watanabe, and T Oda
March 1988, The Japanese journal of antibiotics,
S Matsuda, and M Suzuki, and T Shimizu, and M Ishikawa, and A Souma, and S Fujimoto, and S Makinoda, and T Chimura, and T Watanabe, and T Oda
March 1992, The Japanese journal of antibiotics,
Copied contents to your clipboard!