This prospective multicenter cohort study enrolled 120 patients who had undergone total knee replacement surgery (TKA) at four major hospitals. The primary exposure was short-term intravenous flurbiprofen axetil (FA) postoperatively, with a comparator group of normotensive patients implied within the cohort analysis.
The main renal outcomes—blood urea nitrogen, serum creatine, and Cystatin C levels—showed no statistically significant main effects of group, time, or group-by-time interaction (all P > 0.05). Urine N-acetyl-beta-glucosaminidase (NAG) levels were significantly higher on postoperative day 2 (POD2) and POD5 in both groups versus baseline (all P < 0.001). In the well-controlled hypertensive group, NAG levels continued to increase on POD5 (P = 0.039).
Acute kidney injury (AKI) incidence was 7.0% (4/57) in the well-controlled hypertensive group and 3.2% (2/63) in the normotensive group (P = 0.335). After adjustment, hypertension had no impact on AKI (OR = 0.733; 95%CI: 0.074–7.222, P = 0.790). FA significantly reduced pain intensity in both groups, with no significant differences in other complications.
All AKI cases were stage 1. The study did not report serious adverse events, discontinuations, or detailed tolerability data. Key limitations include the observational design, which precludes causal inference, and the focus on well-controlled hypertensive patients, limiting generalizability.
Practice relevance is restrained: the FA regimen appears effective for pain without increasing AKI incidence in this specific population, though the risk of tubular damage was noted as a consideration.
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BackgroundCurrently, postoperative nonsteroidal anti-inflammatory drugs-associated kidney damage in hypertensive patients remains undetermined. This study aimed to examine renal safety of short-term post-surgery use of flurbiprofen axetil (FA) in well-controlled hypertensive patients.MethodsData were collected from January 2020 to March 2021 at four major hospitals on patients who had undergone total knee replacement surgery (TKA). Patients were divided into well-controlled hypertensive and normotensive groups, and received short-term intravenous FA postoperatively. The primary outcomes were trajectory changes of postoperative renal injury biomarkers. Second outcomes included acute kidney injury (AKI), pain intensity and other complications.ResultsA total of 120 patients were enrolled. Post-surgery FA significantly reduced pain in both groups. The results of repeated measures analysis of variance (ANOVA) demonstrated that the main effects of group, time and the group-by-time interaction on blood urea nitrogen (BUN), serum creatine (SCr) and Cystatin C (Cys C) levels were not statistically significant on postoperative day 2 and 5 (POD2 and POD5) (all P > 0.05). Urine N-acetyl-beta-glucosaminidase (NAG) levels were significantly higher on POD2 and POD5 in both groups [preoperative: (6.66 ± 4.87) U/L, POD2: (10.07 ± 6.88) U/L, POD5: (10.25 ± 7.68) U/L in normotensive group; preoperative: (7.39 ± 4.07) U/L, POD2: (12.34 ± 7.1) U/L, POD5: (15.57 ± 12.34) U/L in well-controlled hypertensive group; all P < 0.001] compared with baseline. However, only the well-controlled hypertensive group showed a continued increase in NAG levels on POD5 (P = 0.039). AKI occurred in 7.0% (4/57) and 3.2% (2/63) of well-controlled hypertensive and normotensive patients (P = 0.335), and all the AKI patients were at stage 1. After adjusting for confounding factors, hypertension had no impact on AKI (OR = 0.733, 95%CI: 0.074–7.222, P = 0.790). No significant differences in other complications were observed between the groups.ConclusionThe current FA regimen after surgery is effective, and it does not increase AKI incidence in well-controlled hypertensive TKA patients, thought posing a risk of tubular damage.