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Vol 44 # 2 June 2012 - Kma.org.kw

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121<br />

KUWAIT MEDICAL JOURNAL<br />

<strong>June</strong> <strong>2012</strong><br />

Original Article<br />

Determining the Effect of Sufentanil<br />

on Propofol Injection Pain<br />

Tuba Berra Saritas, Hale Borazan, Inci Kara, Sema Tuncer, Seref Otelcioglu<br />

Department of Anesthesiology and Reanimation, Selcuk University Meram Medical School, Konya, Turkey<br />

Kuwait Medical Journal <strong>2012</strong>; <strong>44</strong> (2): 121 - 124<br />

ABSTRACT<br />

Objectives: Propofol is a general anesthetic. Its most<br />

important disadvantage is pain on injection. Our aim was<br />

to evaluate the effectiveness of sufentanil on propofol<br />

injection pain (PIP).<br />

Design: Case control randomized double-blind study<br />

Setting: Anesthesia department of Selcuk University<br />

Meram Medical School , Turkey<br />

Subjects: A total of 160 adults, 18 to 65 years, ASA I-II<br />

patients, scheduled for operations under general anesthesia,<br />

were enrolled in this study. A 22-gauge intravenous (IV)<br />

catheter was inserted into a vein on the dorsum of the<br />

hand. Patients were randomly allocated to one of four<br />

groups to receive either saline or 0.5, 1, 2 mcg sufentanil<br />

in 2 ml volume. Thirty seconds after the intravenous (IV)<br />

injection of the pretreatment drug, 5 ml of 1% propofol at<br />

room temperature (Fresenius Kabi, Hamburg, Germany)<br />

was injected IV at rate of 0.5 ml/sec. Pain was assesed<br />

verbally and scored as none (0), mild (1), moderate (2),<br />

severe (3).<br />

Interventions: Prior injection of sufentanil or placebo<br />

Main Outcome Measures: Severity of PIP<br />

Results: Demographic data were comparable among<br />

four groups. Sufentanil at 1 and 2 mcg doses significantly<br />

decreased pain incidence when compared to the saline<br />

group (p < 0.05). Sufentanil 0.5 mcg had no effect (p ><br />

0.05). Although 2 mcg sufentanil decreased the incidence<br />

of PIP more than 1 mcg, there was no significant difference<br />

between these groups (p > 0.05).<br />

Conclusion: Sufentanil at one and 2 mcg doses reduced<br />

the incidence and severity of PIP<br />

KEY WORDS: general anesthesia, pain, propofol, sufentanil<br />

INTRODUCTION<br />

Propofol is a frequently used intravenous (IV)<br />

anesthetic for induction of anesthesia and for sedation<br />

in daycase surgery. The most important disadvantage<br />

of propofol is injection pain, which is reported in 28<br />

- 90% of patients [1] .<br />

Many different methods have been proposed to<br />

reduce the incidence and severity of this adverse<br />

effect of propofol. Pretreatment with alfentanil [2] , use<br />

of fentanyl [3] , local anesthetics [4] , metoclopramide [5] ,<br />

tramadol [6] , ketamine [7] , ondansetron [8] , addition of<br />

lidocaine [9,10] , alfentanil [11] ephedrine [12] , granisetron [13] ,<br />

and injection of propofol into a large antecubital vein<br />

or into a freely flowing intravenous (IV) line, are<br />

the techniques described for prevention of propofol<br />

injection pain (PIP) .<br />

Fentanyl, remifentanil, alfentanil and sufentanil<br />

can provide analgesia and assist anesthetic effects<br />

when used as presurgical medication, induction or<br />

maintenance agents, for postsurgical pain relief and<br />

neurolept and neuroleptanalgesia and as supplements<br />

to regional anesthesia. Opioids are also reported to<br />

be effective in preventing PIP [3,10,11] . Sufentanil is a<br />

selective μ receptor agonist, 5-10 times more effective<br />

analgesic than fentanyl and with a high safety [14] .<br />

However, there are few studies in literature that<br />

report sufentanil analgesic effect on PIP. In this study<br />

we tried to evaluate effectiveness of sufentanil, in<br />

prevention of PIP.<br />

SUBJECTS AND METHODS<br />

Ethics Committee approval was obtained from<br />

Selcuk University Meram Medical Faculty. All<br />

patients gave their informed and written consent.<br />

A total of 160 adult, aged between 18 to 65 years,<br />

ASA physical status I-II patients, scheduled for<br />

operations under general anesthesia, were enrolled<br />

into this randomized, double-blind study conducted<br />

in 2006 at the anesthesiology department of Meram<br />

Medical School of Selcuk University. Patients with<br />

Address correspondence to:<br />

Tuba Berra Saritas, MD, Associate Professor, Selcuk University Meram Medical School, Department of Anesthesiology and Reanimation,<br />

Konya,Turkey. Tel: 90 3322236166, Fax: 90 3322236181, E-mail:erdemtugba@hotmail.com

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