Comparison of parturient - controlled remifentanil with epidural bupivacain and sufentanil for labour analgesia: randomised controlled trial
Jazyk angličtina Země Česko Médium print-electronic
Typ dokumentu srovnávací studie, časopisecké články, randomizované kontrolované studie
PubMed
23128818
DOI
10.5507/bp.2012.073
Knihovny.cz E-zdroje
- MeSH
- anestetika lokální aplikace a dávkování MeSH
- bolest farmakoterapie MeSH
- bupivakain aplikace a dávkování MeSH
- dospělí MeSH
- epidurální analgezie * MeSH
- komplikace porodu farmakoterapie MeSH
- lidé MeSH
- měření bolesti MeSH
- mladý dospělý MeSH
- opioidní analgetika aplikace a dávkování MeSH
- pacientem kontrolovaná analgezie * MeSH
- piperidiny aplikace a dávkování MeSH
- porod MeSH
- prospektivní studie MeSH
- remifentanil MeSH
- sufentanil aplikace a dávkování MeSH
- těhotenství MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- mladý dospělý MeSH
- těhotenství MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- randomizované kontrolované studie MeSH
- srovnávací studie MeSH
- Názvy látek
- anestetika lokální MeSH
- bupivakain MeSH
- opioidní analgetika MeSH
- piperidiny MeSH
- remifentanil MeSH
- sufentanil MeSH
INTRODUCTION: Epidural analgesia (EA) has significant contraindications including coagulation disorders and parturient refusal. One alternative is intravenous self-administered analgesia using the ultra short-acting opioid remifentanil (rPCA). We compared the efficiency and safety of standard epidural analgesia with parturient-controlled intravenous analgesia using remifentanil as well as personal satisfaction. MATERIALS AND METHODS: We enrolled twelve ASA I classified women with singleton pregnancy who delivered vaginally in the period 3/2010-5/2010 and who received rPCA (n=12) in standard analgesic protocol: 20 µg boluses using PCA pump with a lockout interval of 3 min. The control group consisted of 12 pregnant women who received EA (n=12): 0.125% bupivacaine with sufentanil 0.5 µg/mL in top-up boluses every hour until delivery. Data were acquired from standard Acute Pain Service (APS) form and patient medical records (demographic, labour course parameters), Visual Analogue Scale (VAS), Bromage Scale (BS) and adverse effects of analgesia. RESULTS: There were no demographic or labour course parameter differences between groups (P>0.05). The differences in VAS decrease (P=0.056) and parturient satisfaction (P=0.24) during the whole analgesia administration were statistically insignificant. The main limitation of the study was small sample and enrolment of healthy singleton pregnant women only. CONCLUSION: Remifentanil use in obstetric analgesia is a viable alternative to EA, especially in cases of EA contraindications and parturient disapproval.
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