The Optimal Dosage of Intrathecal Morphine for Peripartum Analgesia
Status: | Recruiting |
---|---|
Conditions: | Women's Studies |
Therapuetic Areas: | Reproductive |
Healthy: | No |
Age Range: | 18 - 50 |
Updated: | 2/7/2015 |
Start Date: | July 2010 |
Contact: | Philip Hess, MD |
Email: | phess@bidmc.harvard.edu |
Phone: | 6176673112 |
The purpose of this study is to determine the ideal dosage of intrathecal morphine for intra
and post partum analgesia, while minimizing the side effect profile.
and post partum analgesia, while minimizing the side effect profile.
Regional anesthesia techniques such as combined spinal epidural (CSE) analgesia are very
effective for the management of intrapartum pain. The advantages of these techniques are
that they are safe when properly conducted and that they provide excellent analgesia while
allowing the patient to remain awake and participate in the labor and delivery. The risks of
maternal aspiration and fetal drug depression associated with general anesthesia are
minimized. Finally, the effective analgesia associated with regional techniques blunt the
hemodynamic effects caused by painful contractions and reduce maternal catecholamines,
resulting in increased placental perfusion.1
Opioids in combination with local anesthetics in the spinal space provide effective pain
relief during labor with minimal side effects. The advantages of spinal opioid
administration include lack of motor blockade and faster onset of analgesia.2 In addition,
since the opiate receptors are in the spinal space, a smaller amount of opioid can be used
to provide excellent pain relief while minimizing the side effects. At Beth Israel
Deaconess Medical Center (BIDMC), the obstetric anesthesiology group uses a standard spinal
dosing for CSE during labor which includes: 1 ml of 0.25% bupivicaine with 12.5 mcg of
fentanyl.
Yeh and colleagues have found that morphine 150 mcg added to the fentanyl-bupivicaine spinal
injection can prolong the duration of spinal analgesia but was associated with increased
side effects. 3 The side effect profile of spinal narcotics include: nausea, vomiting,
pruritus, and urinary retention. Although these side effects for the most part can be easily
treated, they can be bothersome to the post partum patient. In a previous study performed
from our institution, the addition of 100 mcg of morphine to spinal bupivicaine and fentanyl
reduced the rate of breakthrough pain during labor analgesia and prolonged the time to first
request for supplementation. Overall, it was found that the incidence of side effects was
low but the group that received the spinal morphine did have more nausea and vomiting
compared with the placebo group. 4
In this current investigation, we would like to assess whether an even smaller dose of
spinal morphine would provide an effective, pain free recovery from vaginal delivery while
decreasing the incidence of side effects, specifically nausea and vomiting. We would like to
perform a formal dose response study to identify the ideal dose of intrathecal morphine that
would not compromise the pain relief during labor while minimizing the side effects.
effective for the management of intrapartum pain. The advantages of these techniques are
that they are safe when properly conducted and that they provide excellent analgesia while
allowing the patient to remain awake and participate in the labor and delivery. The risks of
maternal aspiration and fetal drug depression associated with general anesthesia are
minimized. Finally, the effective analgesia associated with regional techniques blunt the
hemodynamic effects caused by painful contractions and reduce maternal catecholamines,
resulting in increased placental perfusion.1
Opioids in combination with local anesthetics in the spinal space provide effective pain
relief during labor with minimal side effects. The advantages of spinal opioid
administration include lack of motor blockade and faster onset of analgesia.2 In addition,
since the opiate receptors are in the spinal space, a smaller amount of opioid can be used
to provide excellent pain relief while minimizing the side effects. At Beth Israel
Deaconess Medical Center (BIDMC), the obstetric anesthesiology group uses a standard spinal
dosing for CSE during labor which includes: 1 ml of 0.25% bupivicaine with 12.5 mcg of
fentanyl.
Yeh and colleagues have found that morphine 150 mcg added to the fentanyl-bupivicaine spinal
injection can prolong the duration of spinal analgesia but was associated with increased
side effects. 3 The side effect profile of spinal narcotics include: nausea, vomiting,
pruritus, and urinary retention. Although these side effects for the most part can be easily
treated, they can be bothersome to the post partum patient. In a previous study performed
from our institution, the addition of 100 mcg of morphine to spinal bupivicaine and fentanyl
reduced the rate of breakthrough pain during labor analgesia and prolonged the time to first
request for supplementation. Overall, it was found that the incidence of side effects was
low but the group that received the spinal morphine did have more nausea and vomiting
compared with the placebo group. 4
In this current investigation, we would like to assess whether an even smaller dose of
spinal morphine would provide an effective, pain free recovery from vaginal delivery while
decreasing the incidence of side effects, specifically nausea and vomiting. We would like to
perform a formal dose response study to identify the ideal dose of intrathecal morphine that
would not compromise the pain relief during labor while minimizing the side effects.
Inclusion Criteria:
- singleton pregnancy,
- at least 36 weeks gestational age,
- active labor (≤ 5 cm dilation) requesting neuraxial analgesia,
- ASA I or II,
- not currently taking pain medications.
Exclusion Criteria:
- multiple gestation,
- preterm labor,
- systemic opioids in the past 4 hours,
- chronic pain syndromes,
- chronic opioid use,
- contraindications to regional anesthesia,
- allergies to opioids,
- significant co existing medical problems,
- severe pregnancy induced hypertension,
- sedatives,
- magnesium therapy,
- diabetes type 1.
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