Maternal perception of sound-provoked fetal movement as a test of antepartum fetal wellbeing.

Maternal perception of sound-provoked fetal movement test was studied on 506 occasions in 443 women with obstetric or medical antenatal risk factors after 26 weeks gestation. The response was compared with a nonstress test (NST) performed immediately after a three-second vibroacoustic stimulation with an electronic artificial larynx. A positive response to sound stimulation, recorded as a fetal movement by the mother, occurred on 497 occasions (97.3%) and was accompanied by a reactive NST on 484 occasions; giving a specificity of 99.6 per cent and a negative predictive value of 97.4 per cent. An inconclusive or negative response to sound (2.7%) had a sensitivity of 35.0 per cent and a positive predictive value for a nonreactive NST of 77.8 per cent. Results of sound-provoked fetal movement test and NST, performed within a week of delivery, in 434 women were compared with fetal outcome. The maternal perception of sound-provoked fetal movement test had better specificity (99.1% vs 96.9%), positive predictive value (55.6% vs 35.0%) for poor fetal outcome than the NST, although its sensitivity (50.0% vs 70.0%) and negative predictive value (98.8% vs 99.3%) were lower. Maternal perception of sound-provoked fetal movement test may suffice as an inexpensive and simple method of evaluating antepartum fetal well-being in risk situations. When the mother does not feel any sound provoked fetal movement, NST is then performed. This clinical application can be helpful in a primary health care setting where rapid assessment of fetal health at risk is required.

Rapid karyotyping in the second and third trimesters for fetuses at risk of chromosomal abnormalities at Chulalongkorn Hospital.

Transabdominal fetal blood sampling under ultrasonic guidance was performed in 20 fetuses at 18 to 34 weeks gestation. Pure fetal blood was obtained in all cases; 11 from the umbilical veins at the placental cord insertion, 7 from the fetal intrahepatic veins and 2 from the fetal hearts. Rapid karyotype was obtained within 7 days by fetal lymphocyte culture. Chromosomal abnormality was detected in 5 (25.0%) fetuses. Abnormal karyotype was found in 4 of 8 fetuses with structural malformations detected by antenatal ultrasound and in 1 of 5 fetuses of elderly mothers at advanced gestational ages. This suggested that in fetuses at risk of chromosomal abnormality, rapid karyotype should be obtained and fetal blood sampling is justified in the second or third trimester.

Intrauterine growth retardation: incidence, screening results, pregnancy outcome.

Intrauterine growth retardation is detrimental to the health of fetuses and neonates both immediately and in the long run. A risk scoring system to help screen for this complication has been developed as a result of this prospective study. With the incidence of intrauterine growth retardation at approximately 9 per cent in this study population, the final risk scoring system with its 6 variables and total score of 10 was found to be quite useful as a screening method because of its high sensitivity (91.18%) and high negative predictive value (98.14%). Screening by this risk scoring system should be helpful and prove practical among health personnel with varying levels of expertise and experience. Most gravidae had easy labour and delivered within 24 hours. Instrumental delivery rate was high with caesarean section rate of 17.6 per cent. Almost 70 per cent of the intrauterine growth retarded babies were symmetrical type and the perinatal mortality rate in this group was 42.3 which is approximately 4 times that in general population delivered at this hospital.

Rapid Plasma Reagin test (RPR) compared to Venereal Diseases Research Laboratory test (VDRL) for the diagnosis of syphilis in pregnancy.

Obstetric departments which provide service for a large number of patients from different parts of the country and socioeconomic backgrounds like the Obstetric Department of Chulalongkorn hospital, need to develop rapid laboratory tests which can cope with the volume of work and yet provide sound laboratory data for management decisions. We, therefore, undertook a study of the suitable Rapid Plasma Reagin (RPR) test as a diagnostic tool for syphilis in 9,347 pregnant women who attended antenatal clinics at this institute from August 1984 to May 1985. The RPR test was used in addition to the routine serological tests for syphilis namely the VDRL, TPHA and/or FTA-ABS. Analysis of results confirmed that the RPR test fulfilled all laboratory results for clinical requirements. The results from RPR and VDRL were not significantly different. Their sensitivities were 90.86 and 89.95 per cent, their specificities were 99.57 and 99.68 per cent, their positive predictive values were 82.11 and 85.92 per cent, their negative predictive values were 99.8 and 99.78 per cent, and their accuracy was 99.39 and 99.47 per cent respectively. In our study it was found that the RPR test could provide a laboratory diagnosis in 60-90 minutes; in the same morning period when 15-20 prenatal patients were seen for the first time. The above results suggest that the RPR test is a rapid and reliable tool which is particularly suitable for syphilis screening in a busy antenatal clinic. The test enabled all 197 patients with syphilis in pregnancy to be treated promptly and without any loss of follow-up.(ABSTRACT TRUNCATED AT 250 WORDS)

Treatment of sexual contacts of syphilitic pregnant women.

Between August 1984 and May 1985, 197 syphilitic pregnant women were diagnosed at the antenatal clinic, Department of Obstetrics & Gynaecology, Faculty of Medicine, Chulalongkorn University. One hundred and sixty-nine male sexual contacts were serologically tested for syphilis and seventy-eight cases were found positive. Twenty-eight cases refused to be tested. Thirty-two syphilitic male contacts had cerebrospinal fluid tests and four were found to be abnormal. Fifty-three cases or 67.9 per cent of 78 syphilitic male consorts did not complete a full diagnostic and treatment protocol. They preferred to be treated with benzathine penicillin G 2.4 million units intramuscularly for 3 consecutive weeks. After this treatment no patient agreed to a repeat spinal tap. This behavioral attitude concurred with their socioeconomic background. All were from a low socioeconomic group and lacked health knowledge. This made it difficult to work with them and contributed to inadequate management of their disease.

Effectiveness of benzathine penicillin regimen in the treatment of syphilis in pregnancy.

The intramuscular injection of benzathine penicillin G 2.4 million units weekly for 3 consecutive weeks to syphilitic pregnant women was again confirmed to be clinically effective for prevention of their neonates from congenital syphilis and well accepted as treatment for syphilis in pregnancy. It was administered to 184 cases, or 93.5 per cent, of 197 syphilitic gravidas. It was found that pregnancy outcomes in terms of abortion, stillbirth, prematurity, full term delivery, neonatal birth weight, macroscopic examination of the placenta and general physical examination of the neonate were clinically useful as a parameter to evaluate the effectiveness of the therapy for the infant. Clinical symptoms and signs in the mother, serological tests for syphilis in the gravida and cord blood of the newborn, and placental weight were not useful in the evaluation of adequacy of treatment of our study group.