Minipercutaneous Nephrolithotomy Under Mixture of Local Anesthesia: A Randomized Controlled Study

To evaluate the safety, efficacy, and feasibility of minipercutaneous nephrolithotomy (MPCNL) under mixture of local anesthetics (MLA) vs spinal anesthesia (SA) for management of large renal stones. This study was a prospective randomized controlled study and approved by IRB (REC-FOMBU). A total of 120 consecutive patients who met the inclusion criteria of the study and agreed to sign the informed consent form were randomized to undergo MPCNL under MLA (60 patients) or SA (60 patients). Intra- and postoperative findings including visual pain analogue scale (VAS), operative time, hospital stay, adverse events (AEs), stone-free rate, and related data were recorded. Baseline characteristics and demography included age and gender; stone's site, size, and density were comparable for both groups (p > 0.05). The average VAS scores in the MLA group at 0, 2, 6, 12, and 24 hours were 2.5, 0, 1, 1, and 0, respectively. The corresponding values in the SA group were 2, 1, 2, 2, and 1, respectively, (p < 0.05). The average operation time was ∼1 hour for both groups and the length of hospital stay was 1.5 days for both groups (p > 0.05). Whereas the mean hemoglobin deficit was 1.04% ± 0.54% vs 1.27 ± 0.46 (p = 0.013) and the primary postoperative stone clearance was 93.4% vs 88.3% (p > 0.05), for MLA and SA groups, respectively. Postoperative analgesic consumption and complications were similar in the MLA and SA groups. Single tract MPCNL is feasible under either MLA or SA with comparable stone clearance and AEs. Perioperative VAS was similar and acceptable for both modalities.