Placement of Bupivacaine-soaked Spongostan in Episiotomy Bed Is Effective Treatment Modality for Episiotomy-associated Pain
| Autor: | Nilgün Öztürk Turhan, Hasan Kafali, Candan İltemur Duvan, Elif Gözdemir, Serap Simavli |
|---|---|
| Rok vydání: | 2008 |
| Předmět: |
Adult
Episiotomy medicine.medical_specialty Visual analogue scale medicine.medical_treatment Birth weight Gestational Age law.invention Diclofenac Randomized controlled trial Pregnancy law medicine Birth Weight Humans Anesthetics Local Bupivacaine Pain Postoperative business.industry Obstetrics and Gynecology Gestational age Fibrin Foam medicine.disease Surgery Parity Anesthesia Female business medicine.drug |
| Zdroj: | Journal of Minimally Invasive Gynecology. 15:719-722 |
| ISSN: | 1553-4650 |
| Popis: | To investigate the efficacy of placing bupivacaine-soaked Spongostan (Ferrosan, Soeborg, Copenhagen, Denmark) in episiotomy beds for relief of postpartum pain.Randomized, controlled study (Canadian Task Force classification I).University medical school.Women with mediolateral episiotomy.Patients were recruited and randomized into 2 groups by using a random number table. Group I (control group) received local lignocaine infiltration 1% up to 20 mL. For group II (Spongostan group), in addition to local lignocaine infiltration, bupivacaine-soaked Spongostan was placed in the episiotomy bed. All patients received routine postpartum perineal care in addition to the regular pain drugs (75 mg of diclofenac every 4 hours if needed). The primary outcome for the study was severity of pain, rated on a 10-cm visual analog scale from 0 to 10. Rating was recorded at 0, 1, 1.5, 2, 6, and 24 hours after delivery.In all, 48 women were randomized to group I (local lignocaine alone) and 51 women to group II (local lignocaine plus Spongostan). The Spongostan and control groups were similar with respect to maternal age, parity, gestational age, maternal weight, and neonatal birth weight (p.05; CI for difference: -2.6/10, 0.1/0.3, 0.3/0.7, 6.9/1.7, and -7/1.9, respectively). Episiotomy length (both vaginal and perineal) and episiotomy depth were higher in Spongostan group than control group (p.05; 95% CI: -0.9/0, -0.8/-0.1, and -0.6/0, respectively). However, episiotomy reconstruction time of both groups was similar (p.05; CI: 1.7/6.2). The pain score of Spongostan group was lower than control group and it was statistically significant at all time intervals (0, 1, 1.5, 2, 6, and 24 hours) between the Spongostan and control groups (p.05; CI: 0.6/1.9, 1.1/2.4, 1.0/2.5, 0.9/2.4, 0.3/1.9, and 0.5/1.8, respectively). Postpartum total analgesic requirement (mg/person) again was significantly lower in the Spongostan group than control group (p.01; CI: 0.1/0.4).Placement of bupivacaine-soaked spongostan into the episiotomy bed resulted in decreased postpartum pain and drug requirement. It may be attributed to a higher drug concentration at episiotomy bed and prolonged drug effect. |
| Databáze: | OpenAIRE |
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