R Sim, D Cheong, KS Wong, B Lee, QY Liew Tan Tock Seng Hospital Singapore

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Prospective randomized, double-blind, placebo-controlled study of pre- and postoperative administration of a COX-2- specific inhibitor as opioid-sparing analgesia in major colorectal resections R Sim, D Cheong, KS Wong, B Lee, QY Liew Tan Tock Seng Hospital Singapore

Postoperative ileus (POI) is a problem POI is inflammatory in origin 1 Pain relief is another problem Opioids and POI 1. Kreiss C, Birder LA, Kiss S, et al. COX-2 dependent inflammation increases spinal Fos expression during rodent postoperative ileus. Gut 2003 Apr; 52(4):527-34.

Hypothesis Patients treated with Valdecoxib, a COX-2-specific inhibitor, will have reduced postoperative ileus and a shorter recovery when compared with a standard postoperative patient-controlled analgesia (PCA) morphine only regimen after colorectal resections.

Aims Demonstrate the reduction of postoperative ileus and opioid-sparing effect with the use of a COX-2- specific inhibitor administered preand post-operatively in patients undergoing major colorectal surgery.

Patients and Methods One institution from Dec 2002 to Jun 2004 Randomized, double-blind, placebo-controlled In the study arm, the first dose of Valdecoxib 40mg was administered orally as close to one hour prior to the start of surgery. Each subsequent dose was administered at 24-hour intervals up to 120h. Patients in the control arm were served placebos at the same timings.

Patients and Methods The primary endpoint for calculating sample size was days to first bowel movement. A sample size of 40 patients per group is sufficient to detect a difference of 1 day (25%, assuming average 4 days to first bowel movement) with at least 80% power and type I error of 0.025 (for a two-sided test adjusted for two treatment comparisons).

Patients and Methods Inclusion Criteria: The patient is a male or female of more than 18 years of age and requires elective colorectal resection including cancers is in satisfactory health as determined by the Investigator on the basis of medical history and physical examination ASA class I-III is able to use PCA has provided written informed consent prior to admission to this study

Patients and Methods Exclusion Criteria: The patient has sulfonamide allergy. requires emergency surgery / laparoscopic assisted surgery has inflammatory bowel disease needs epidural or other regional analgesia has known opioid intolerance or inability to use PCA has known acetylsalicylic acid or NSAIDs hypersensitivity has active peptic ulcer disease, asthma, coagulopathy, or renal failure is pregnant or lactating uses conventional NSAIDs, COX-2 inhibitors, or tramadol during the six hours preceding surgery, during surgery or subsequent to the end of surgery is required to take muscle relaxants, tricyclic antidepressants, tranquilizers, sedatives, hypnotics or neuroleptics in the postoperative period

Patients and Methods PCA morphine was used for analgesia uniformly and stopped when there was adequate analgesia with Paracetamol 1g p.o. q6hr prn. Pain assessments completed after resting supine for at least 15 minutes. Clear liquid diet on the POD1. Once oral intake exceeds 30ml/kg of body weight without nausea or vomiting, diet was advanced to a low-fat, gastrointestinal diet. Evaluated every 12 hours, once in the morning and again in the evening for the endpoints of bowel sound, flatus and bowel movement. Discharged when 1) tolerating a solid diet, 2) passing flatus, 3) without fever or other medical problem requiring hospitalisation.

Study Placebo Patient characteristic (n = 40) (n = 39) P Age (years) Mean (SD) 61.0 (11.4) 63.1 (10.4) 0.585 Range 24-77 39-78 Sex Male 20 (50.0%) 18 (46.0%) 0.654 Female 20 (50.0%) 21 (54.0%) Medical Problems* (COAD, Hypt, DM, IHD) Yes 26 (65.0%) 24 (62.0%) 0.777 No 14 (35.0%) 15 (38.0%) BMI Mean (SD) 23.0 (3.7) 23.0 (3.7) 0.511 Range 17.8-33.2 16.0-33.0 Diagnosis Colorectal cancer 36 (90.0%) 39 (100.0%) 0.136 Benign (sigmoid diverticulitis, 4 (10.0%) 0 sigmoid volvulus)

Study Placebo Patient characteristic (n = 40) (n = 39) P Type of Operation Anterior Resection (AR) 15 (37.5%) 16 (41.0%) 0.158 AR (with extended resection) 6 (15.0%) 2 (5.1%) Low AR 4 (10.0%) 4 (10.2%) Low AR with stoma 3 (7.5%) 1 (2.6%) Hartmann s Procedure 3 (7.5%) 0 Abdomino-Perineal Resection 1 (2.5%) 4 (10.0%) Hemicolectomy 5 (12.5%) 11 (28.2%) Others (small bowel resection, 3 (7.5%) 1 (2.6%) panprotocolectomy, Hartmann s reversal) Stoma - Yes 8 (20.0%) 5 (12.8%) 0.405 No 32 (80.0%) 34 (87.2%) Incision Length (cm) Mean (SD) 17.8 (11.1) 17.0 (4.2) 0.436 Range 10-25 7-28 Duration of Operation (min) Mean (SD) 158.0 (61.1) 152.0 (55.3) 0.733 Range 65 320 75 300

30% reduction at 24h, 45% reduction at 48h 30% reduction at 24h, 45% reduction at 48h

Median 12h vs 24h

Median 36h vs 48h

Median 72h vs 84h

Median 24h vs 24h

Median 60h vs 72h

Results Placebo group - 3 had breakthrough pain that required intercostals nerve blocks and 1 patient had an AMI on POD 4. Study group - 3 patients had breakthrough pain separately requiring intercostal nerve block, intramuscular pethidine and oral tramadol; 1 patient had an anastomotic dehiscence.

Study Placebo Patient characteristic (n = 40) (n = 39) P Length of Stay (days) Mean (SD) 4.9(2.7) 6.3(2.3) 0.009 Median 4.0 6.0 Range 2-19 4-14 Hospitalization Cost ($) Mean(SD) 11 210(14 510) 8 767(2 188) 0.447 Median 8 652 8 673 Range 6 115 98 524 6 324-15 025

Major morbidity (%) Study Placebo (n = 6) (n = 7) P Acute myocardial infarct 0 1 (14.2) 0.317 Anastomotic dehiscence 1 (16.6) 0 Pnuemonia 1 (16.6) 2 (28.5) Minor morbidity (%) Urinary tract infection 0 1 (14.2) 0.317 Wound related 2 (33.3) 1 (14.2) Prolonged ileus 0 2 (28.5) Thrombophlebitis 1 (16.6) 0 Postoperation confusion 1 (16.6) 0 Readmission within 30 days (%) (n = 5) (n = 3) Adhesion colic 1 (20.0) 2 (66.6) 0.317 Bleeding per rectum/stoma 2 (40.0) 1 (33.3) Stoma related 1 (20.0) 0 Wound related 1 (20.0) 0

Discussion Preemptive analgesia works in major abdominal bowel surgery Oral works, Parenteral not required Could not demonstrate the degree to which the preemptive administration of the COX-2 inhibitor contributed to the observed benefits of reduction of POI and opioid usage POI was also reduced probably as result of (1) reduced opioid usage, (2) early ambulation with better pain control and (3) attenuated inflammatory response Did not address the relative contribution of each factor toward the reduction of postoperative ileus though it is evident that all these factors can be attributed to COX-2 inhibtion

Asao T, Kuwano H, Nakamura J, et al. Gum chewing enhances early recovery from postoperative ileus after laparoscopic colectomy. J Am Coll Surg 2002 Jul; 195(1):30-2.

Le Blanc-Louvry I, Costaglioli B, Boulon C, et al. Does mechanical massage of the abdominal wall after colectomy reduce postoperative pain and shorten the duration of ileus? Results of a randomized study. J Gastrointest Surg 2002 Jan-Feb; 6(1):43-9.

Walch JM, Rabin BS, Day R, et al. The effect of sunlight on postoperative analgesic medication use: a prospective study of patients undergoing spinal surgery. Psychosom Med. 2005 Jan-Feb; 67(1): 156-63.

Conclusions Postoperative ileus is multifactorial in origin and hence a multimodal approach is likely to be the best means to enhance postoperative recovery. The addition of an oral COX-2-specific inhibitor pre- and postoperatively can reduce opioid use, postoperative ileus and length of stay when compared with a standard postoperative patientcontrolled analgesia (PCA) morphine regimen after colorectal resection.