Related Experiment Video
Updated: Jan 22, 2026

Author Spotlight: Evaluating the Adjuvant Efficacy and Safety of Angong Niuhuang Pill in Viral Encephalitis Treatment
Published on: April 19, 2024
Adenosine antagonists for prevention of contrast-induced nephropathy: A meta-analysis of randomized controlled trials
Hongbin Zang1, Qiongyu Zhang2, Xiaodong Li1
1Department of Cardiology, Shengjing Hospital of China Medical University, Shenyang, Liaoning 110004, P.R. China.
Insights
Adenosine antagonists (AAs) may reduce contrast-induced nephropathy (CIN) and serum creatinine levels. However, trial sequential analysis indicates more evidence is needed to confirm the benefit of AAs in preventing CIN.
Area of Science:
- Nephrology
- Pharmacology
- Clinical Trials
Background:
- Contrast-induced nephropathy (CIN) is a complication of intravascular contrast agent administration.
- The effectiveness of adenosine antagonists (AAs) in preventing CIN is currently debated.
Purpose of the Study:
- To evaluate the efficacy of adenosine antagonists (AAs) in preventing contrast-induced nephropathy (CIN).
- To assess the reliability of pooled results using trial sequential analysis (TSA).
Main Methods:
- A meta-analysis of randomized controlled trials (RCTs) comparing AAs with controls was conducted.
- Searched Medline, Embase, Web of Science, and Cochrane databases for relevant studies.
- Assessed heterogeneity, publication bias, study quality, and performed sensitivity, cumulative, subgroup, and TSA analyses.
Main Results:
- A total of 17 trials with 1,483 subjects were included.
- Pooled results showed AAs significantly reduced CIN incidence (RR, 0.53; 95% CI, 0.29-0.95) and serum creatinine levels (SMD, -0.24; 95% CI, -0.44 to -0.04).
- TSA indicated that the required information size was not reached for CIN incidence, suggesting a risk of false-positive results.
Conclusions:
- Current meta-analysis data suggest AAs can reduce CIN incidence and serum creatinine levels post-contrast media administration.
- However, TSA highlights the need for additional evidence to definitively confirm the benefits of AAs in CIN prevention.
- Further research is required to establish the role of AAs in managing CIN.
Abstract:
Contrast-induced nephropathy (CIN) is caused by intravascular administration of contrast agent. The efficacy of adenosine antagonists (AAs) in preventing CIN remains controversial, and its elucidation was the objective of the present meta-analysis. A trial sequential analysis (TSA) to assess the reliability of the pooled results was also performed. The Medline, Embase, Web of Science and Cochrane databases were searched to retrieve all published randomized controlled trials (RCTs) comparing AAs with controls in preventing CIN. Heterogeneity, publication bias and quality of studies were assessed. Sensitivity, cumulative and subgroup analyses were also performed. The risk of random errors was evaluated by TSA. A total of 17 trials with 1,483 subjects were included. Pooled results indicated that AAs significantly reduced the incidence of CIN [risk ratio, 0.53; 95% confidence interval (CI), 0.29-0.95; P=0.034] and the serum creatinine (SCr) level after contrast media (CM) administration (standardized mean difference, -0.24; 95% CI, -0.44 to -0.04; P=0.019). Meta-regression did not identify any significant source of heterogeneity. In the subgroup analyses, AAs tended to exhibit a greater prevention efficacy in trials with sample sizes of ≥70, baseline SCr of <1.5 mg/dl and low study quality. TSA on the incidence of CIN indicated that the required information size determined as n=1,778 was not reached, and that the cumulative Z-curve did not cross the TSA boundary. In conclusion, the present meta-analysis of data from current RCTs suggested that AAs reduce the incidence of CIN and the SCr levels after CM administration. However, TSA showed that the risk of having a false-positive result was greater than 5% in the meta-analysis of the incidence of CIN, indicating that more evidence is required to ensure the benefit of AAs in preventing CIN.
Related Concept Videos
Statistical Software for Data Analysis and Clinical Trials
Clinical Trials
There are four phases in a clinical trial. A phase one...
Clinical Trials: Overview
Trial and Error and Algorithm
Chemotherapy-Induced Nausea and Vomiting: Dopamine Receptor Antagonists
Phenothiazines, such as prochlorperazine...
Chemotherapy-Induced Nausea and Vomiting: 5-HT3 Receptor Antagonists

