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H Wulf

Publications and source records attributed to H Wulf.

168 records · Page 10Linked to original sources

Cholestasis as a side effect of bupivacaine?

BACKGROUND AND OBJECTIVES: Cholestasis has been proposed as a side effect of interpleural bupivacaine. Therefore, the effects of various application techniques on liver enzymes were studied following ethics committee approval and informed patient consent. METHODS: Patients following scheduled thoracotomy and laparoscopic cholecystectomy were prospectively studied and randomized to the following application techniques of bupivacaine: Thoracic surgery. T0: Control (systemic analgesia only: patient-controlled analgesia with opioids; n = 26); T1: Repetitive intercostal blocks (10-20 mL 0.5% bupivacaine, 2-4 times per day for 3-6 days; n = 17); T2: Interpleural injections via a catheter placed intraoperatively (20 mL 0.25%, 4-6 times per day for 3-6 days, right: n = 25 or left: n = 12). Laparoscopic cholecystectomy. Intraperitoneal application (single injection). L0: 50 mL saline (Control) (n = 21). L1: 50 mL 0.125% bupivacaine (n = 18); L2: 50 mL 0.25% (n = 20). The serum concentrations of bilirubin, gamma-GT, alkaline phosphatase, leucine amino peptidase, glutamate oxalacetate transaminase, and glutamate pyruvate transaminase were measured preoperatively and on day 1, 3, and 7 postoperatively. RESULTS: Neither application of plain bupivacaine was associated with significant changes in the postoperative concentration of hepatic enzymes. In particular, there was no difference between left- and right-sided interpleural application. Although increases in hepatic enzyme concentrations were observed in some patients postoperatively, this was similar in the bupivacaine and control groups. CONCLUSION: Perioperative interpleural, intercostal, and intraperitoneal administration of bupivacaine was not associated with findings indicative of cholestasis in the early postoperative course.

Adult↗

Clinical usefulness, safety, and plasma concentration of ropivacaine 0.5% for inguinal hernia repair in regional anesthesia.

BACKGROUND AND OBJECTIVE: The aim of this study was to evaluate the pharmacokinetics, feasibility, and clinical effects of ropivacaine in regional anesthesia (ilioinguinal-iliohypogastric blocks [IIB], genitofemoral block plus local infiltration) for inguinal hernia repair. METHODS: Following ethics committee approval and informed consent, 21 male adults received 60 mL ropivacaine 0.5% (without vasoconstrictor). In 11 patients, further injections of 5 to 10 mL were given while preparing the hernial sack. Plasma concentration of ropivacaine was determined in venous blood after 10, 20, 30, 45, 60, 90, 120, and 300 minutes using reversed-phase high pressure liquid chromatography (HPLC). RESULTS: Peak plasma concentrations of ropivacaine were 1.5 +/- 0.6 (0.7 to 2.6) microg/mL (mean +/- SD [range]). These maximum concentrations occurred after 45 (30 to 60) minutes (median [range]). No signs of central nervous or cardiovascular toxicity were observed. Twelve of 21 patients did not need any additional analgesics within 24 hours postoperatively. One patient had a femoral motor block lasting 6 hours, 5 patients reported sensory femoral block lasting 5 to 12 hours. Patients, as well as the surgeon, were very satisfied with the procedure, and all patients stated that they would like to have it performed again that way in case of an inguinal hernia on the opposite side. CONCLUSION: A ropivacaine dose of 60 to 70 mL of 0.5% appears adequate for regional anesthesia for inguinal hernia repair regarding conditions for surgery, safety, ambulation, and postoperative pain relief.

Adult↗

[Precipitable C4-poor immune complexes in HELLP syndrome and pre-eclampsia].

In 16 patients with HELLP syndrome and 10 patients with preeclampsia, laser nephelometric analysis of PEG-precipitated immunocomplexes revealed a decrease in the complement component C4. This is interpreted as a further indication of an immunologic component in the pathogenesis of these disorders.

Adolescent↗

Plasma concentrations of bupivacaine in celiac plexus block.

BACKGROUND AND OBJECTIVES: Following stellate ganglion block, systemic absorption of local anesthetics is rapid. Pharmacokinetic data for local anesthetics following other blocks, such as celiac plexus blocks, are lacking. METHODS: Plasma concentrations of bupivacaine in venous blood samples following celiac blocks were measured in 10 patients using a high-performance liquid chromatography technique; 40 mL plain bupivacaine 0.25% was administered. RESULTS: Celiac plexus block resulted in maximum plasma concentrations of 0.7-2.5 mg/L bupivacaine (mean, 1.5 +/- 0.6 mg/L). In 3 of 10 patients plasma concentrations above 2 mg/L occurred. The maximum concentrations were reached 10-30 minutes after the injection (17 +/- 8 minutes). No clinical signs of central nervous system toxicity occurred. All patients showed hemodynamic stability following the blocks. CONCLUSIONS: Maximum plasma concentrations of bupivacaine occur rather late following celiac blocks compared to stellate ganglion or intercostal blocks. The rather high plasma concentrations of bupivacaine indicate the need for appropriate clinical monitoring.

Adult↗