Evidence map›Paper›PMID 42516486›Full record

ArticleCureus2026

Determinants and Frequency of Acute Kidney Injury After Endoscopic Retrograde Cholangiopancreatography.

Muhammad Minhal Sandhu, Sohaib Ahmad, Muhammad Nibras Mehmood Randhawa, Zailah Mehmood Randhawa, Naimal Mehmood Randhawa, Hafiz Zunair Iqbal, Jahangeer Ahmed, Ammar Noor, Muhammad Irfan Jamil

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Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Muhammad Minhal SandhuAcute Medicine, Southend University Hospital NHS Foundation Trust, Southend, GBR.
Sohaib AhmadMedicine, Pakistan Institute of Medical Sciences, Islamabad, PAK.
Muhammad Nibras Mehmood RandhawaMedicine, Islamabad Medical & Dental College, Islamabad, PAK.
Zailah Mehmood RandhawaMedicine, Rawalpindi Medical University, Rawalpindi, PAK.
Naimal Mehmood RandhawaMedicine, Rawalpindi Medical University, Rawalpindi, PAK.
Hafiz Zunair IqbalInternal Medicine, Akhtar Saeed Medical and Dental College, Lahore, PAK.
Jahangeer AhmedGastroenterology, Lahore General Hospital, Lahore, PAK.
Ammar NoorInternal Medicine, Lahore General Hospital, Lahore, PAK.
Muhammad Irfan JamilNephrology, Lahore General Hospital, Lahore, PAK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEndoscopic retrograde cholangiopancreatography (ERCP) is commonly performed for pancreaticobiliary disorders. However, renal dysfunction may occur after the procedure and can influence clinical outcome. This study was planned to estimate the frequency of acute kidney injury (AKI) following ERCP and to assess the clinical and laboratory factors associated with its occurrence.

methodsThis observational analytical study was conducted at the Department of Gastroenterology, Lahore General Hospital, Lahore, from January 2025 to March 2026. A total of 296 patients undergoing ERCP for choledocholithiasis, obstructive jaundice, biliary stricture, or pancreaticobiliary malignancy were enrolled by non-probability consecutive sampling. Patients with end-stage renal disease, pre-existing AKI, prior renal replacement therapy, renal transplant, or unclear repeat ERCP records were excluded.

resultsAKI was observed within 48 hours after ERCP in 52 (17.6%; 95% CI 13.7-22.3%) patients. Most AKI cases were KDIGO Stage 1 (37/52, 71.2%), followed by Stage 2 (9/52, 17.3%) and Stage 3 (6/52, 11.5%). Patients who developed AKI had a higher mean age than those without AKI (61.2 ± 13.8 vs. 52.4 ± 14.9 years, p = 0.001). The Charlson Comorbidity Index (CCI) was also significantly raised in the AKI group (5 (IQR 3-6) vs. 3 (IQR 2-4); p < 0.001). Acute cholangitis was the commonest ERCP indication among patients with AKI as compared with those without AKI (31/52 (59.6%) vs. 58/244 (23.8%), p < 0.001). Baseline renal function was worse among patients who developed AKI, with higher serum creatinine (1.42 ± 0.68 vs. 0.84 ± 0.31 mg/dL) and lower estimated glomerular filtration rate (58.4 ± 28.7 vs. 84.6 ± 24.3 mL/min/1.73 m²), with both comparisons showing statistical significance (p < 0.001). Mean hospital stay was also longer in patients with AKI (9.4 ± 5.1 vs. 6.1 ± 3.6 days, p < 0.001). On multivariable analysis, CCI, acute cholangitis, reduced eGFR, raised bilirubin, low albumin level, and exposure to nephrotoxic drugs or intravenous contrast were identified as independent determinants of post-ERCP AKI.

conclusionPost-ERCP AKI is an important renal complication and was mainly associated with greater comorbidity burden, acute cholangitis, reduced baseline renal function, raised bilirubin, low serum albumin, and prior nephrotoxic drug or intravenous contrast exposure. Careful pre-procedural renal assessment and early post-procedural monitoring may help identify high-risk patients and reduce adverse clinical outcomes.

Indexed as

acute kidney injuryendoscopic retrograde cholangiopancreatography (ercp)estimated glomerular filtration ratepost-ercp pancreatitis (pep)risk factors

Identifiers

PMID42516486
PMCPMC13405356

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