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Intrathecal morphine plus general anesthesia in cardiac surgery: effects on pulmonary function, postoperative
Luciana Moraes dos Santos1, Verônica Cavani Jorge Santos, Silvia Regina Cavani Jorge Santos
1Department of Anesthesia, Heart Institute, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil. lumoraesrj@yahoo.com.br
Objectives:
To evaluate the effects of intrathecal morphine on pulmonary function, analgesia, and morphine plasma concentrations after cardiac surgery.
Introduction:
Lung dysfunction increases morbidity and mortality after cardiac surgery. Regional analgesia may improve pulmonary outcomes by reducing pain, but the occurrence of this benefit remains controversial.
Methods:
Forty-two patients were randomized for general anesthesia (control group n=22) or 400 microg of intrathecal morphine followed by general anesthesia (morphine group n=20). Postoperative analgesia was accomplished with an intravenous, patient-controlled morphine pump. Blood gas measurements, forced vital capacity (FVC), forced expiratory volume (FEV), and FVC/FEV ratio were obtained preoperatively, as well as on the first and second postoperative days. Pain at rest, profound inspiration, amount of coughing, morphine solicitation, consumption, and plasma morphine concentration were evaluated for 36 hours postoperatively. Statistical analyses were performed using the repeated measures ANOVA or Mann-Whiney tests (*p<0.05).
Results:
Both groups experienced reduced FVC postoperatively (3.24 L to 1.38 L in control group; 2.72 L to 1.18 L in morphine group), with no significant decreases observed between groups. The two groups also exhibited similar results for FEV1 (p=0.085), FEV1/FVC (p=0.68) and PaO2/FiO2 ratio (p=0.08). The morphine group reported less pain intensity (evaluated using a visual numeric scale), especially when coughing (18 hours postoperatively: control group= 4.73 and morphine group= 1.80, p=0.001). Cumulative morphine consumption was reduced after 18 hours in the morphine group (control group= 20.14 and morphine group= 14.20 mg, p=0.037). The plasma morphine concentration was also reduced in the morphine group 24 hours after surgery (control group= 15.87 ng.mL-1 and morphine group= 4.08 ng.mL-1, p=0.029).
Conclusions:
Intrathecal morphine administration did not significantly alter pulmonary function; however, it improved patient analgesia and reduced morphine consumption and morphine plasma concentration.
Insights
Intrathecal morphine improved pain relief and reduced morphine use and plasma levels after cardiac surgery, without significantly impacting pulmonary function. This offers a potential benefit for postoperative recovery.
Area of Science:
- Anesthesiology
- Cardiothoracic Surgery
- Pharmacology
Background:
- Post-cardiac surgery lung dysfunction is a major cause of mortality.
- Regional analgesia may improve pulmonary outcomes by mitigating pain.
- The efficacy of regional analgesia in improving pulmonary function post-cardiac surgery is debated.
Purpose of the Study:
- To assess the impact of intrathecal morphine on pulmonary function.
- To evaluate the analgesic effects of intrathecal morphine.
- To measure morphine plasma concentrations following cardiac surgery.
Main Methods:
- A randomized trial comparing general anesthesia with intrathecal morphine plus general anesthesia.
- Pulmonary function tests (FVC, FEV) and blood gas analysis were performed.
- Pain scores, morphine consumption, and plasma morphine levels were monitored postoperatively.
Main Results:
- Intrathecal morphine did not significantly alter forced vital capacity (FVC), forced expiratory volume (FEV), or oxygenation.
- Patients receiving intrathecal morphine reported significantly lower pain intensity, especially during coughing.
- Morphine consumption and plasma morphine concentrations were significantly reduced in the intrathecal morphine group.
Conclusions:
- Intrathecal morphine effectively improves analgesia after cardiac surgery.
- It leads to reduced overall morphine consumption and lower plasma concentrations.
- No significant adverse effects on pulmonary function were observed.
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