Dexamethasone Bupivacaine Versus Bupivacaine
Dexamethasone Bupivacaine Versus Bupivacaine
Dexamethasone Bupivacaine Versus Bupivacaine
Research Article
KEYWORDS Abstract Aim: The study conducted aims to assess the efficacy, time to first analgesic request, and
Bupivacaine; postoperative inflammatory response after adding dexamethasone to local anesthetic mixture for a
Dexamethasone; peribulbar block in posterior segment eye surgery.
Posterior segment; Patients and methods: A double-blind randomized study was carried out on 50 ASA I and II
Vitreoretinal; patients scheduled for elective posterior segment surgery (vitreoretinal). Patients were allocated ran-
Peribulbar block domly into two groups, 25 patients in each group. Group I received equal volumes of 10 ml of a l:1
mixture of bupivacaine 0.5% and saline, supplemented with 4 mg dexamethasone in 1 ml saline and
group II received the same local anesthetic mixture (total volume 10 ml) without adding dexameth-
asone. The duration and onset of motor block, time to first analgesic request, postoperative inflam-
matory response, and other side effects such as nausea and vomiting were assessed.
Results: Patients receiving peribulbar block were significantly pain free by end of surgery (0 h)
(P < 0.05) and throughout the postoperative period in the dexamethasone group at 2 and 6 h postop-
eratively. The number of patients requiring rescue analgesics was significantly lower with dexameth-
asone bupivacaine block (P < 0.05). The incidence of postoperative nausea and vomiting was
significantly less in the first group (I) in comparison to the other group (II) (P < 0.05) and lastly
the level of C reactive protein postoperatively was found to be significantly less in the dexamethasone
group than the other one (P < 0.0001).
Conclusion: Adding dexamethasone to bupivacaine in peribulbar block appears to be a safe and clin-
ically superior adjuvant with less postoperative pain, inflammatory response in patients undergoing
posterior segment eye surgery.
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http://dx.doi.org/10.1016/j.egja.2013.07.003
408 M.S. Mahmoud et al.
Table 4 Pain assessment at 2, 6, and 12 h postoperatively. (Number of patients who were pain free postoperatively).
Time 0H 2H 6H 12 H
Group I (dexamethasone + bupivacaine) N = 23 21/23 19/23 21 /23 23/23
(91.3%) (82.6%) (91.3%) (100)
Group II (Bupivacaine) N = 25 20/25 12/25 15 /25 23/25
(80%) (48%) (60) (92)
P value P = 0.48 P = 0.027\ P = 0.03\ P = 0.507
Non-significant Significant Significant Non-significant
Data are expression as number percent.
tween the two groups as regard the onset of lid and globe aki- was performed using student t-test. Comparison between cate-
nesia (p > 0.05, Table 2). gorical data was performed using the chi-squared test. Data
The duration of lid akinesia was longer (158.26 ± were considered significant if p values were <0.05. Statistical
13.42 min.) in group I than in group II (148.52 ± 12.61 min.) analysis was performed with the aid of the MEDCALC com-
and this was statistically significant (P < 0.05) (Table 3). Also, puter program (version 12 windows).
the duration of globe akinesia was longer (188.16 ±
12.35 min.) in group I than in group II (179.02 ± 11.58 min.) 4. Discussion
and this was statistically significant (P < 0.05) (Table 3).
Number of patients who were pain free was less in group II Our study was a prospective, double blinded, randomized
at 2, 6 h postoperatively, in comparison with group I and this study. The primary outcome was the effect of dexamethasone
was statistically significant (P < 0.05) (Table 4), and they were on the duration and quality of peribulbar block and the sec-
almost non-significantly different at 12 h duration postopera- ondary outcome was the confirmation of the efficacy of adding
tively. The number of patients requiring postoperative analge- dexamethasone for prolongation of postoperative analgesia
sia at 2, 6 h postoperatively were significantly less in group I and the anti-inflammatory effect as well. Dexamethasone was
(bupivacaine–dexamethasone group) (P < 0.05) (Table 5); not used before as an adjuvant to local anesthetic for ophthal-
moreover, the time to first analgesic request was significantly mic block but used alone intravitreally, subconjunctival, and in
longer in group I (P < 0.05) than in group II (Table 5). peribulbar injection [12].
The inflammatory response to the surgery was assessed The results of our study indicate that the addition of dexa-
postoperatively by measuring the levels of C – reactive protein methasone to bupivacaine for peribulbar block in posterior
which was significantly less in group I in comparison with segment surgery had led to prolongation of duration of lid
group II P < 0.05) (Table 6). As regard postoperative nausea and globe akinesia; the time of first rescue analgesia was de-
and vomiting, in group 1 (bupivacaine–dexamethasone group) layed together with prolonged postoperative analgesic dura-
only one patient developed nausea and vomiting while in tion indicated by prolonged duration of akinesia and VAS.
group II 3 patients, and this was statistically non-significant The result of our study is in agreement with the analgesia
(P > 0.05) (Table 7). effects of preoperative administration of dexamethasone and
Results are expressed as means ± standard deviation (SD) other glucocorticoids given by oral, intravenous, intramuscu-
or number percent (%). Comparison between numerical data
410 M.S. Mahmoud et al.
Table 5 Comparison between dexamethasone group and the bupivacaine group in no. of patients requiring analgesia postoperative
(pain score > or equal 4 on VAS) also time for first analgesic request.
0H 2H 6H 12 H
Group I (Dexamethasone + Bupivacaine) (N = 23) 0/23 2/23 1 /23 0/23
(0%) (8.69%) (4.34%) (0%)
Group II (Bupivacaine) (N = 25) 5/25 11/25 8/25 2/25
(20%) (44%) (32) (8%)
P value P = 0.073 P = 0.015\ P = 0.037\ P = 0.5
Table 6 Inflammatory response assessment postoperatively, using C reactive protein levels (lg/dl).
Preoperatively 24 h Postoperatively
Group I (dexamethasone + bupivacaine) N = 23 1.39 ± 1.46 6.37 ± 2.11 lg/mL
Group II (bupivacaine) N = 25 1.62 ± 1.84 15.63 ± 3.14 lg/mL
P value =0.635 Non-significant P < 0.0001 highly significant
Data are expressed as mean + SD.
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