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* From the Department of Ophthalmology Eye Hospital, Faculty of Clinical Medicine Mannheim, University of Heidelberg Mannheim, Germany, and
the Department Of Anesthesiology, Centre Hospitalier de l'Université de Montréal (CHUM), University of Montréal, Montréal, Québec, Canada.
Address correspondence to: Dr. J. Jonas, Universitäts-Augenklinik, Theodor-Kutzer-Ufer 1-3, 68167 Mannheim, Germany. Phone: **49-621-383-2652; Fax: **49-621-383-3803; E-mail: Jost.Jonas{at}augen.ma.uni-heidelberg.de
| Abstract |
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Methods: This prospective noncomparative clinical interventional case-series study included 43 consecutive patients undergoing scleral buckling procedures as treatment of rhegmatogenous retinal detachments. Using a commercially available retrobulbar needle with a diameter of 0.80 mm and a length of 38 mm, 7 mL of local anesthetic were injected into the retrobulbar space. Through the same needle, a 28-gauge commercially available flexible spinal anesthesia catheter was introduced into the retrobulbar space, the needle was withdrawn, and the catheter was fixed. The catheter was removed on the morning of the first postoperative day. When the patients started to feel pain during or after surgery, 2 mL of local anesthetic were re-injected through the catheter.
Results: During surgery, 12 (27.9%) patients received a pain-free re-injection through the retrobulbar catheter resulting in a marked reduction of pain. Two (4.7%) patients needed a second re-injection. In the postoperative period, 23 (53.5%) patients experienced pain of grade 3 or higher 5.4 ± 6.7 hr after start of surgery and received a retrobulbar re-injection. Eleven (25.6%) patients asked for a second postoperative re-injection, and four (9.3%) patients received a third postoperative re-injection. Cardiopulmonary and central nervous adverse effects were not noticed.
Conclusions: Use of an ultra-fine retrobulbar catheter for repeat intraoperative and postoperative injections of local anesthetics is a simple and effective method to achieve analgesia during and after scleral buckling procedures.
| Introduction |
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| Materials and methods |
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The scleral buckling procedure included use of an encircling band (n = 23 patients), a scleral buckle (n = 25), transscleral retinal exocryocoagulation (n = 43), and transscleral exodrainage of the subretinal fluid (n = 25). Mean duration of surgery was 55.2 ± 16.9 min (range, 20105 min). Preoperatively, the patients had routinely received 1 or 2 mg lorazepam orally as sedative medication.
Using a commercially available custom-made retrobulbar needle (length: 38 mm) with an outer diameter of 0.80 mm (Geuder GmbH, Hertzstrasse, D-99126 Heidelberg, Germany), 7 mL of mepivacaine 2% (n = 37), bupivacaine 0.50% (n = 2) or ropivacaine 0.75% (n = 4) were injected from the temporal inferior position transcutaneously into the retrobulbar space prior to the operation. Through the needle in place, a 28-gauge catheter (Kendall GmbH, D-93333 Neustadt, Germany), the same that is used for spinal anesthesia, was introduced into the retrobulbar space, and the needle was withdrawn. After removal of the stylet from the catheter, a 0.20 µ bacterial filter was attached, the catheter taped to the skin, and 1 mL of local anesthetic injected to purge the catheter.
During surgery, the patients were monitored and asked every ten to 15 min, whether they were comfortable or experienced pain. In a similar manner, the patients were asked regularly after surgery whether they started to feel pain. For this purpose, we had explained a pain scale to the patients with 0 for no pain and 10 for maximal pain. Each time the patients started to feel painful sensations of grade 3 or higher on the pain scale, 2 mL of local anesthetic were re-injected. The catheters were removed on the morning of the first postoperative day.
| Results |
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Intraoperatively, 12 (27.9%) patients asked for a re-injection after which a pain score of less than 2 was achieved within one to two minutes of injection. Mean interval between start of the operation and the first re-injection was 36.3 ± 30.6 min (median, 30 min; range, 5 to 100 min). Two (4.7%) patients needed a second re-injection, 20 to 55 min after start of surgery. A re-injection was performed in three of 17 (17.6%) patients with a duration of surgery shorter than 50 min, in seven of 19 (36.8%) patients with a duration of surgery longer than 50 min, and in four of nine (44.4%) patients with a duration of surgery longer than 60 min. Mean volume of mepivacaine administered during surgery was 11.2 ± 2.1 mL (median, 11 mL; range, 816 mL). At the end of surgery, a subconjunctival injection of gentamicine was given and did not cause pain of grade 3 or higher.
Postoperatively, 23 (53.5%) patients experienced pain of grade 3 or higher 5.4 ± 6.7 hr after the start of surgery and received a re-injection of the local anesthetic which markedly reduced pain to grade 0 to 2 on the pain scale. Eleven (25.6%) patients asked for a second postoperative re-injection 6.0 ± 4.9 hr after the start of surgery, and four (9.3%) patients received a third postoperative re-injection 9.3 ± 3.3 hr after the start of surgery. Cardiopulmonary and central nervous adverse effects were not noticed by the attending anesthesiologist.
The mobility of the patients in the postoperative period was not restricted by the catheter. The patients could move around freely, read the newspapers or watch television. Asked whether they would receive this kind of postoperative local anesthesia again, 90.7% of the patients answered positively. The remaining patients were either undecided or preferred a re-operation under general anesthesia.
| Discussion |
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Revision received February 12, 2002. Accepted for publication December 20, 2001.
| References |
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Bernard JM, Hommeril JL. Prolonged peribulbar anaesthesia with indwelling catheter: a preliminary report of 217 cases. Br J Anaesth 1997; 78 : 812.
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