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Biomedical subjects

T Penny-MacGillivray

Publications and source records attributed to T Penny-MacGillivray.

2 recordsLinked to original sources

Intravenous meperidine infusion for obstetric analgesia.

OBJECTIVE: To provide safe, satisfying obstetric analgesia when epidural analgesia was unavailable. DESIGN: Randomized, controlled study of women in labor. SETTING: A regional hospital offering primary- and secondary-level obstetric care. PARTICIPANTS: Thirty-nine women with low-risk, single, term pregnancies and anticipated vaginal delivery. INTERVENTIONS: Women in the intermittent intramuscular (IM) injection group received meperidine 50-100 mg, every 2 hours, as required. Those in the intravenous (IV) infusion group received an initial bolus of meperidine 25 mg, a basal infusion rate of 60 mg/h, and intermittent boluses of 25 mg/h as required. Each participant had a maximum of 200 mg of meperidine available to her during labor. MAIN OUTCOME MEASURE: Pain intensity was measured on a 10-cm visual analogue scale. Pain ratings were recorded when analgesia was initiated and every 30 minutes thereafter, until delivery. RESULTS: Women who received IV meperidine reported significantly lower levels of pain (p = .0015) than women in the IM group. However, women in the IV group received significantly higher doses of meperidine (mean = 121 mg) than those in the IM group (mean = 82 mg; p = .0007). When pain scores were compared on a smaller group of participants (n = 18) who received similar doses of meperidine (100-150 mg), women in the IV group still reported lower pain scores (p = .0092). No significant differences were found between the groups in length of labor, maternal vital signs, fetal heart rate, Apgar scores, level of maternal sedation, or patient-reported side effects. CONCLUSION: IV meperidine infusion was superior to intermittent IM injections for pain relief during labor.

Adolescent↗

A newborn's first bath: when?

OBJECTIVE: To determine the effects of early admission bathing on thermoregulation in newborns. DESIGN: Randomized, comparative study. SETTING: A regional hospital providing primary and secondary newborn care. PARTICIPANTS: One hundred healthy, full-term newborns. INTERVENTIONS: Newborns in the investigational group with a minimum rectal temperature of 36.5 degrees C. were bathed after the newborn admission assessment examination was completed (M = 61.15 minutes of age), whereas newborns in the control group were bathed at the standard of 4 hours of age (M = 252.12 minutes of age). MAIN OUTCOME MEASURE: Rectal temperatures were measured using a Diatek thermometer. Rectal temperatures were recorded during the newborn admission assessment examination, immediately before bathing, immediately after bathing, 1 hour after bathing, and 2 hours after bathing. RESULTS: No significant differences (p < .05) in rectal temperatures, were found between the groups during the admission assessment examination, before bathing, immediately after bathing, 1 hour after bathing, or 2 hours after bathing. No significant differences were found between the groups in type of delivery, time of birth, gestational age, birth weight, Apgar scores at 1 and 5 minutes, air temperature, apical heart rate, or respiratory rate. CONCLUSIONS: Healthy, full-term newborns whose rectal temperatures are greater than 36.5 degrees C can be bathed immediately after the admission assessment examination.

Analysis of Variance↗