Author, date and country | Patient group | Study type (level of evidence) | Outcomes | Key results | Study Weaknesses |
---|---|---|---|---|---|
Kim JA, et al. 2009 Korea | 52 patients scheduled for VATS lobectomy were randomly allocated to one of two groups - either epidural patient controlled analgesia (PCA) or IV PCA. 37 patients completed the study (74%) - 18 in epidural PCA group, 19 in IV PCA group. | 2b - Individual low quality RCT (<80% of patients finished study) | Pain Scores | No significant differences between the groups | The study was not blinded to prevent any potential effects of researcher/patient bias. Pain scores were only tested at 1 hour and 24 hours post-operatively, potentially missing increases in pain in the first day. |
Daily morphine consumption | No significant differences between the groups | ||||
Forced vital capacity | No significant differences between the groups | ||||
Forced expiratory volume in 1 second | No significant differences between the groups | ||||
Satisfaction score | No significant differences between the groups | ||||
Incidence of side effects | No significant differences between the groups | ||||
Hill SE, et al. 2006 USA | 80 patients undergoing unilateral thoracoscopic procedures, double blinded randomisation into two groups (n=40) of either study group or placebo group. | 1 b - Prospective, double-blinded, randomised clinical trial | Intraoperative fentanyl usage | Treated group had significantly less intraoperative fentanyl (p=0.003) | Single use paravertebral block only used, no group withmultiple doses. Patients were low-risk and no emergency operations were undertaken. |
Postoperative patient-controlled morphine usage (first 6 hours) | Treated group had a 31% smaller cumulative patient-controlled morphine dose (P=0.03) | ||||
Postoperative patient-controlled morphine usage 12 and 18 hours) | No significant differences between the groups | ||||
Visual analog pain score | Lower scores were reported in the treated group (P=0.02) | ||||
Cytokine production | No significant differences between the groups | ||||
Cortisol levels | No significant differences between the groups | ||||
Vogt A, et al. 2005 UK | 45 patients were randomly allocated to two groups for treatment with a paravertebral block - treatment group and placebo control. 40 patients completed the study (n=20 in each group). | 1 b - Prospective, randomised clinical trial | Pain scores | The treatment group has significantly less pain than the control group (P<0.05) | Small patient numbers. Results were taken as cumulative over 48 hours, and more intensive monitoring over a longer period may have improved the validity of the results. |
Cumulative morphine consumption | No significant differences between the groups | ||||
Peak expiratory flow rate | No significant differences between the groups | ||||
Side-effects | No significant differences between the groups | ||||
Fernandez MI, et al. 2005 UK | 112 patients (77 male, 45 female) who underwent a total of 118 VATS pleurectomies (66 right- and 52 left-sided) for spontaneous pneumothorax. 22 patients received epidural analgesia, the remaining | 3b - Individual case-control study. | Time for patients to receive oral analgesia alone | Higher in control group (56 hours (12-144)) compared to Intrathecal analgesia patients (20 hours (0-96)) (p<0.001) | No randomisation of patients. Retrospective nature of the study. Small proportion of patients were in the intrathecal analgesia group (~19%). |
Post-operative VAS pain score in the morning of first day after surgery | No significant difference. | ||||
Peak post-operative VAS pain score at any point during recovery. | No significant difference. | ||||
Incidence of long-term complications | No significant difference. |