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* From the Departments of Anaesthesia and
¶ Obstetrics and Gynaecology, Rotunda Hospital, Dublin, Ireland;
Anaesthesia, The Robert Jones Agnes Hunt Orthopedic Hospital, Oswestry, United Kingdom;
Anaesthesia, Cork University Hospital, Cork, Ireland;
Anaesthesia, Beaumont Hospital, Dublin, Ireland.
Address correspondence to: Dr. Conan McCaul, Departments of Anaesthesia and Critical Care Medicine, Hospital for Sick Children, 555 University Avenue, Toronto, Ontario M5G 1X8, Canada. Phone: 416-813-7445; Fax: 416-813-7543; E-mail: conan.mccaul{at}utoronto.ca
| Abstract |
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Methods: We compared iv fluid loading with and without supplementary dextrose for the prevention of postoperative nausea and vomiting (PONV). In a prospective double-blinded controlled trial, 120 ASA I female patients undergoing elective gynecological laparoscopy were randomized to one of three groups, and received either: (a) CSL 1.5 mLkg-1 per hour fasting duration; (b) CSL, 1.5 mLkg-1 per hour fasting duration with 0.5 gkg-1 dextrose added in 50% formulation (CSL/dextrose); or (c) no iv fluid (control).
Results: Compared with control the percentage of patients who had no PONV within 24 hr of anesthesia in the CSL and CSL/dextrose groups was 78% vs 83% and 71%, P = 0.81 and P = 0.683 respectively. The numbers needed-to-harm for causing PONV episodes in CSL/dextrose vs CSL or control groups were 5.7 [95% confidence interval (CI), 5.575.91] and 8.2 (95% CI, 8.018.37) respectively. The number needed-to-treat for prevention of PONV episodes in CSL vs control was 19.2 (95% CI, 19.0819.37). A greater proportion of patients in the CSL/dextrose group required narcotic analgesia in the postanesthetic care unit compared to those in the control group (16/35 vs 7/37, P = 0.03). The CSL/dextrose group also demonstrated hyperglycemia (serum glucose 14.0 ± 3.94 vs 5.0 ± 1.01 vs 5.2 ± 0.9 mmolL-1, P < 0.0001) in the postanesthetic care unit compared to the CSL and control groups. The CSL/dextrose group also reported increased thirst at 24 hr compared to control (20/35 vs 11/37, P = 0.035).
Conclusion: These findings suggest that: 1) administration of dextrose is associated with nausea, increased opioid requirement and late thirst after elective gynecological laparoscopy; 2) iv fluids did not decrease PONV.
| Introduction |
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We examined the hypothesis that: (a) supplementary dextrose would reduce the incidence of PONV, and (b) administration of balanced salt solution would also reduce such symptoms.
| Methods |
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= 0.05, ß = 0.8). To allow for dropouts we randomized a total of 120 patients.
Statistical analysis
Statistics were performed using Sigma Stat©, (version 2.0 Jandel Scientific, Chicago, IL, USA). P < 0.05 was considered significant. ANOVA, Students t test and Chi-square were used as appropriate. Quantitative analyses of effect was assessed by calculation of the numbers needed-to-treat (NNT), numbers needed-to-harm (NNH) and 95% confidence intervals (CI).
| Results |
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2 and P = 0.683,
2 respectively. The NNH for PONV episodes in CSL/dextrose vs CSL or control were 5.7 (95% CI, 5.575.91) and 8.2 (95% CI, 8.018.37) respectively. The NNT for PONV episodes in CSL vs control was 19.2 (95% CI, 19.0819.37). The CSL/dextrose group was more hyperglycemic than control or CSL groups (P < 0.0001,
2) in the PACU. More CSL/dextrose patients received fentanyl in the PACU than the control group (46.7% vs 8.9%, P = 0.03,
2). Thirst was increased in the CSL/dextrose group at 24 hr compared to control (P = 0.035,
2). | Discussion |
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Differences exist between our study and those of previous investigators. Yogendran et al. did not allow for fasting duration and the anesthetic technique had important confounding variability.4 Reduced dizziness, headache and sore throat were demonstrated by Cook et al.3 in patients given dextrose. The higher incidence of nausea in our study in the CSL/dextrose group (NNH 5.7) may be explained by our earlier patient assessment. The immediate postoperative period was associated with hyperglycemia in our patients in the CSL/dextrose group. Hyperglycemia is known to reduce gastric emptying and increase sensation of gastric fullness5 and is associated with adverse neurological,6 cardiovascular,7 gastrointestinal5 and immunological8 effects. The previously demonstrated small benefit in subjective postoperative recovery symptoms may be insufficient to justify administration of solutions that cause hyperglycemia.
Opioids may reduce postoperative nausea by reducing pain, indicating a complex interaction between nociception, emesis and analgesia. The relationship between dextrose administration and pain has not to our knowledge been previously described. Glucose loading has been shown to elevate plasma cholecystokinin9 which is involved in modulating pain and altering acute tolerance to opiates.10 In our study, fentanyl administration in the PACU was more frequent in the CSL/dextrose than control indicating a possible relationship between hyperglycemia and opioid tolerance. Because acute hyperglycemia is also associated with increased sensitivity to gastric distension,5 the observed increase in fentanyl consumption in the CSL/dextrose group may indicate a hyperglycemia mediated increase in sensitivity to autonomic components of visceral nociception.
This study has potential limitations. First, this data may not be generalizable to different patient populations, lengthier or different surgical procedures, anesthetic techniques or all formulations of dextrose containing fluids. Second, individualized fluid therapy calculated to replace the deficit incurred by fasting may be impractical. Finally, the secondary hypothesis - that iv fluids would reduce the incidence of PONV - was not proved. However, it was not disproved, and here the issue of sample size is important. The a priori sample size estimates proved adequate to test the primary hypothesis. Post hoc sample size calculation (
0.05, ß 0.80) indicates that with nausea as low as reported in the current study over 600 patients per group would be required to demonstrate that iv fluid significantly decreases nausea. Expressed as NNT, this calculates as 19.2 patients treated for a single patient to benefit, which is far less than that of conventional antiemetics, suggesting that such treatment would have limited clinical usefulness.
| Conclusion |
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| Acknowledgments |
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| Footnotes |
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Revision received February 12, 2003. Accepted for publication August 12, 2002.
| References |
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2 Aitkenhead A, Smith G. Appendix VIb: intraoperative fluid requirements - adult. In: Smith G, Aitkenhead AR. Textbook of Anaesthesia, 3rd ed. London: Churchill Livingstone; 1996: 748.
3 Cook R, Anderson S, Riseborough M, Blogg CE. Intravenous fluid load and recovery. A double-blind comparison in gynaecological patients who had day-case laparoscopy. Anaesthesia 1990; 45: 82630.[Medline]
4 Yogendran S, Asokumar B, Cheng DC, Chung F. A prospective randomized double-blinded study of the effect of intravenous fluid therapy on adverse outcomes on outpatient surgery. Anesth Analg 1995; 80: 6826.[Abstract]
5 Hebbard GS, Sun WM, Dent J, Horowitz M. Hyperglycaemia affects proximal gastric motor and sensory function in normal subjects. Eur J Gastroenterol Hepatol 1996; 8: 2117.[Medline]
6 Pulsinelli WA, Levy DE, Sigsbee B, Scherer P, Plum F. Increased damage after ischemic stroke in patients with hyperglycemia with or without established diabetes mellitus. Am J Med 1983; 74: 5404.[Medline]
7 Marfella R, Nappo F, De Angelis L, Siniscalchi M, Rossi F, Giugliano D. The effect of acute hyperglycaemia on QTc duration in healthy man. Diabetologia 2000; 43: 5715.[Medline]
8 Marfella R, Esposito K, Giunta R, et al. Circulating adhesion molecules in humans. Role of hyperglycemia and hyperinsulinemia. Circulation 2000; 101: 224751.
9 Hasegawa H, Shirohara H, Okabayashi Y, et al. Oral glucose ingestion stimulates cholecystokinin release in normal subjects and patients with non-insulin-dependent diabetes mellitus. Metabolism 1996; 45: 196202.[Medline]
10 Kissin I, Bright CA, Bradley EL Jr. Acute tolerance to continuously infused alfentanil: the role of cholecystokinin and N-methyl-D-aspartate-nitric oxide systems. Anesth Analg 2000; 91: 1106.
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