Labor Epidural Analgesia Clinical Trial
Official title:
A Randomized Double Blind Clinical Trial Comparing Programed Intermittent Epidural Boluses (PIEB) Versus Patient Controlled Epidural Analgesia (PCEA) With Epidural or Combined Spinal-epidural (CSE) Technique
The investigators have design a randomized double blind clinical trial to know the incidence of breaktrough pain (BP) in high-risk of BP parturients (nulliparous with early cervical dilation) comparing two epidural analgesic regimes: programed intermittent epidural boluses versus patient controlled epidural analgesia. The role of the epidural technique (epidural versus combined spinal-epidural) in the incidence of BP will be also evaluated.
Women in labor receiving epidural analgesia may experience breakthrough pain (BP) that
requires the use of additional medication and that is a source of dissatisfaction with the
analgesic treatment for labor.
The investigators can define two types of BP: 'primary breakthrough pain' is the first moment
when the patient requests analgesia during labor. 'Secondary breakthrough pain' can be
defined as the time a previously effective epidural analgesia turns ineffective.
The BP may have multiple causes, such as delivery progression and catheter misplacement.
There is no single pattern to provide adequate neuraxial analgesia for labor, but for certain
patients and specific clinical situations some methods provide advantages over others.
The choice of a suitable system of epidural drug delivery has an important role in getting
proper analgesia and a low incidence of breakthrough pain during labor. In order to develop
preventive strategies for BP, some clinical scales to estimate its incidence rate have been
described. Among risk factors for BP the investigators can include: Nulliparity, epidural
catheter placement at an earlier cervical dilation, neonatal weight and technique performed
(epidural versus combined spinal-epidural - CSE).
In addition, technological development has offered us new treatment modalities of pain
management during childbirth have evolved recently to improve maternal satisfaction, as well
as to treat and prevent BP: Patient Controlled Epidural Analgesia (PCEA) added or not to a
continuous epidural infusion (CEI), computer integrated PCEA (CI-PCEA) and automatic or
programed intermittent epidural boluses (PIEB).
Nowadays, there is no evidence about the best epidural analgesic treatment or the optimum
epidural punction in order to reduce BP episodes and, hence, increase maternal satisfaction.
Therefore, the investigators have design a randomized double blind clinical trial to know the
incidence of breaktrough pain (BP) in high-risk of BP parturients (nulliparous with early
cervical dilation) comparing two epidural analgesic regimes added to a contiuous infusion of
L-bupivacaine plus fentanyl: programed intermittent epidural boluses versus patient
controlled epidural analgesia. The role of the epidural technique (epidural versus combined
spinal-epidural) in the incidence of BP will be also evaluated.
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