Research article | Open | Open Peer Review | Published:
Sodium bicarbonate-based hydration prevents contrast-induced nephropathy: a meta-analysis
BMC Medicinevolume 7, Article number: 23 (2009)
Contrast-induced nephropathy is the leading cause of in-hospital acute renal failure. This side effect of contrast agents leads to increased morbidity, mortality, and health costs. Ensuring adequate hydration prior to contrast exposure is highly effective at preventing this complication, although the optimal hydration strategy to prevent contrast-induced nephropathy still remains an unresolved issue. Former meta-analyses and several recent studies have shown conflicting results regarding the protective effect of sodium bicarbonate. The objective of this study was to assess the effectiveness of normal saline versus sodium bicarbonate for prevention of contrast-induced nephropathy.
The study searched MEDLINE, EMBASE, Cochrane databases, International Pharmaceutical Abstracts database, ISI Web of Science (until 15 December 2008), and conference proceedings for randomized controlled trials that compared normal saline with sodium bicarbonate-based hydration regimen regarding contrast-induced nephropathy. Random-effects models were used to calculate summary odds ratios.
A total of 17 trials including 2,633 subjects were pooled. Pre-procedural hydration with sodium bicarbonate was associated with a significant decrease in the rate of contrast-induced nephropathy (odds ratios 0.52; 95% confidence interval 0.34–0.80, P = 0.003). Number needed to treat to prevent one case of contrast-induced nephropathy was 16 (95% confidence interval 10–34). No significant differences in the rates of post-procedure hemodialysis (P = 0.20) or death (P = 0.53) was observed.
Sodium bicarbonate-based hydration was found to be superior to normal saline in prevention of contrast-induced nephropathy in this updated meta-analysis.
Contrast agents are administered to millions of procedures annually worldwide. In the USA and Europe, contrast-induced nephropathy (CIN) is the third leading cause of acute renal failure in hospitalized patients, accounting for about 10% of hospital-acquired renal failure . The issue of contrast agent-related risk further gains importance with the growing awareness that even gadolinium-based agents are not harmless and may induce renal damage .
Two mechanisms have been hypothesized to be responsible for CIN development: contrast media-triggered vasoconstriction and development of oxidative stress, that is, intrarenal accumulation of reactive oxygen species. One major underlying hypothesis for application of sodium bicarbonate (NaHCO3) is that the alkalinization of tubular fluid diminishes the production of free oxygen radicals [3, 4]. Pretreatment with sodium bicarbonate is more protective than sodium chloride in animal models of acute ischemic renal failure .
Previous meta-analyses have shown a significant benefit for NaHCO3 in comparison to normal saline (NS) infusion [6, 7], although they highlighted the possibility of publication bias. Two trials published thereafter did not show an advantage of NaHCO3 [8, 9], while multiple smaller studies have published preliminary but rather contradictory results [10, 11]. A recent retrospective study suggested even possible harm of NaHCO3 . Given these conflicting results, an updated meta-analysis is meaningful. The purpose of this study was to evaluate the current published and unpublished data regarding the use of NaHCO3 versus NS as pre-procedural hydration for the prevention of CIN.
We searched PubMed, MEDLINE, the Cochrane Central Register of Controlled Trials, International Pharmaceutical Abstracts database, and ISI Web of Science and google scholar from 1990 through to 15 December 2008. In addition, abstract lists and conference proceedings from the 2007 and 2008 scientific meetings of the American College of Cardiology, the European Society of Cardiology, the Transcatheter Cardiovascular Therapeutics, the American Heart Association, the American Society of Nephrology, the European Renal Association, the annual meeting of the Radiology Society of North America Annual, and the World Congress of Cardiology were searched. We also considered published review articles, editorials, and internet-based sources of information (http://www.tctmd.com, http://www.theheart.org) to assess for potential information on studies of interest. Medical subject headings and keyword searches included the terms 'contrast nephropathy', 'sodium bicarbonate', 'saline infusion', 'radiocontrast', and 'renal failure'. Reference lists of selected articles were reviewed for other potentially relevant citations. Authors of selected studies were contacted to obtain further information.
In a two-step selection process, two investigators (HSG and PM) independently reviewed the titles and abstracts of all citations to identify all potentially relevant studies. In a second step, the corresponding publications were reviewed in full text by the same two investigators to assess if studies met the following inclusion criteria: direct comparison of NaHCO3 versus pre-hydration with NS, randomized controlled trial (RCT), and CIN as primary endpoint based on laboratory testing (Figure 1). Reviewers were not blinded to study authors or outcomes. Final inclusion of studies was based on the agreement of both reviewers. Two studies were excluded because they were either retrospective  or because they randomized patients to NS + N-acetyl cysteine (NAC) versus NaHCO3 only .
Data extraction and quality assessment
Two reviewers (PM and UT) extracted relevant information from the articles including baseline clinical characteristics of the study population, laboratory data, baseline creatinine, amount of NS infusion in the control group (total and before contrast administration), type of contrast, average contrast volume and data on primary (CIN) and secondary outcomes, such as mortality, need for hemodialysis (HD). CIN was defined differently by each study, but most described it as an absolute or relative increase in serum creatinine. Seven studies defined CIN as a rise in serum creatinine by 25% or more within 2 to 5 days of contrast exposure [15–21]. Two studies regarded an absolute increase of creatinine of 0.5 mg/dl (= 44 μmol/liter) as their primary definition of CIN [9, 22], whereas six authors used a composite definition of either a 25% relative creatinine increase or an absolute increase of 0.5 mg/dl [8, 11, 23–26]. One study  used change in glomerular filtration rate as the primary endpoint and change in creatinine as a secondary definition for CIN and one abstract  did not mention the CIN definition. For each study we used the corresponding predefined primary endpoint. We assessed trial quality by evaluating specific criteria (concealment of allocation during randomization, intention-to-treat analysis, and blinded assessment of outcome measures), but did not use a quality score in regard to the limitations inherent in such an approach .
Data synthesis and analysis
Data from all the selected studies were combined to estimate the pooled odds ratio (OR) of effect sizes for NS compared with NaHCO3 using a random-effects model. All analyses were performed on an intention-to-treat basis. Continuity correction was used when an event did not occur in one group . Significant between-study heterogeneity was expected regarding study populations, therefore a random-effects model was used to produce across-study summary OR with 95% confidence intervals (CI). We evaluated the presence of heterogeneity across trials with the Q and I2 statistics, with an I2 value > 50% indicating at least moderate statistical heterogeneity. To assess the effect of individual studies on the summary estimate of effect, we did an influence analysis, in which the pooled estimates were recalculated by omitting one study at a time. We assessed publication bias visually (funnel plot) and by formal tests (rank order correlation  and Egger's test of intercept ). A Funnel plot depicts the effect estimates from each trial against study sample size or precision. In absence of publication bias, this plot should appear approximately symmetrical. The Funnel plot is based on the fact that large trials can estimate effects more precisely while smaller trials show wider scattering. A formal measure of Funnel plot asymmetry is the Egger test. It is a linear regression of normalized effects (effect divided by its standard error (SE)) against precision (reciprocal SE of the effect). Very small studies have a larger SE and, consecutively, a normalized effect and a precision that is close to zero. Therefore, the intercept of the regression comes close to zero; if it significantly differs from zero, this indicates systematic deviance of the effect of small studies (small study effect and/or bias, for example, due to publication bias).
We also calculated fail-safe N (that is, the number of studies required to nullify the significant differences in CIN between the two groups) using Rosenberg's and Orwin's method [32, 33]. As there was a suggestion of publication bias, Duval and Tweedie's  Trim and Fill method was used to calculate imputed OR for CIN. Exploratory meta-regression based on a mixed-effect model was performed to estimate the extent to which selected covariates that potentially influence risk for CIN could explain the observed heterogeneity of the NaHCO3 effect (average age of patients, baseline creatinine, volume of contrast medium used, prevalence of diabetic patients in the study, and amount of NS infusion before contrast administration in the control group). Stratified analysis was performed to assess the effect of NaHCO3-based hydration in select groups (patients treated with low osmolar versus iso-osmolar contrast, and those undergoing elective versus emergent procedures) and to assess impact of published versus unpublished studies. All analyses were performed using Comprehensive Meta-Analysis software, version 2.0 (Biostat, Englewood, NJ, USA) and MIX, version 1.7 .
A total of 184 articles were reviewed, and 17 studies satisfied the predetermined inclusion criteria (Figure 1) [8–11, 15–27]. Eight trials have been published in the peer-reviewed literature whereas another nine studies are as yet unpublished but were presented at scientific meetings (that is, Transcatheter Therapeutics meeting, American Heart Association meeting, American Society of Nephrology meeting, World Congress of Cardiology, or Canadian Cardiovascular Congress). Further information on these unpublished trials was obtained from the study authors where possible. One study randomized patients to three arms: NaHCO3, NS, or NS and NAC. From this trial, we used data only from the NaHCO3 and NS arms and excluded the patients randomized to the NS and NAC arm . Data from studies using a 2 × 2 factorial-design testing the influence of NAC and the effect of NaHCO3 were used by pooling patients from the NaHCO3 and NS arms (with or without NAC) [18, 26]. Additional file 1 summarizes the characteristics of the 17 trials, including a total of 2,633 subjects.
CIN occurred in a total of 109 patients in the 1,327 patients of the NaHCO3 arms (range 1.4% to 31.0%) compared with 175 such events in the 1,306 subjects treated with NS (range 2.7% to 34.5%) (Table 1). The summary OR was 0.52 (95% CI 0.34–0.81, P < 0.004) (Figure 2) in favor of NaHCO3. The number needed to treat to prevent one CIN was 16 (95% CI 10–34).
There was moderate heterogeneity across studies regarding clinical patient characteristics and protocols, and also formal tests (I2 = 48.0; Q = 30.6; P value = 0.015).
Stratified analyses suggested a more pronounced effect of NaHCO3 in the two trials including exclusively patients undergoing emergency procedures [22, 24] (OR 0.10; 95% CI 0.02–0.42; P = 0.002) compared with patients undergoing elective procedures (OR 0.63; 95% CI 0.43–0.92; P = 0.017) (Figure 3). Similarly, stratified analysis by the type of contrast medium used suggested lower odds of CIN with NaHCO3 in studies using low-osmolar contrast media [11, 16, 19, 20, 22–25, 27] (OR 0.29; 95% CI 0.15–0.57) compared with those using the iso-osmolar agent iodixanol [8, 9, 15, 18] (OR 0.73; 95% CI 0.32–1.64, P = 0.441) (Figure 4).
Exploratory meta-regression did not identify any significant association between the reduction in CIN with NaHCO3 and any of the baseline variables that were tested (baseline creatinine, NAC use, proportion of patients with diabetes, contrast volume). The eight published trials showed a stronger overall benefit of NaHCO3 (OR 0.4; 95% CI 0.21–0.76, P = 0.005) compared with the nine unpublished studies (OR 0.64; 95% CI 0.34–1.21, P = 0.168) (Figure 5). Furthermore within the published trials, those stopped early [20, 24], demonstrated a much greater reduction in risk of CIN with NaHCO3 (OR 0.12; 95% CI 0.03–0.56, P = 0.007) compared with trials that completed enrolment as planned (OR 0.53; 95% CI 0.28–1.0; P = 0.051). After exclusion of those two trials, the overall OR based on all other studies was 0.60 (95% CI 0.40–0.91; P = 0.016).
The cumulative analysis illustrates the time-course of the OR when performing a meta-analysis after each new study in a chronologic order (Figure 6). This suggests that the initial trials were more likely to show dramatic reduction in CIN with NaHCO3 but subsequent trials have demonstrated more modest benefits.
None of the studies influenced the results to an extent that the conclusion would have changed; the sensitivity analysis omitting one study at a time consistently showed an overall benefit of NaHCO3 compared with NS (Figure 7).
Assessment of publication bias using a funnel plot indicated slight asymmetry (Figure 8), and this was confirmed on formal testing (rank order correlation or Kendall τ of -0.324, one-tailed P value of 0.038, two-tailed P = 0.077, and Egger's test intercept of -1.71, 95% CI of -3.02 to -0.40 with one-tailed P value of 0.007, two-tailed P = 0.014). These tests suggest that the results of this meta-analysis were influenced by a larger treatment effect seen in smaller studies.
The Trim and Fill method was used to calculate a treatment effect based on imputed estimated unpublished studies. The imputed OR for CIN using the random-effects model was 0.62 (95% CI 0.40–0.97). The classic fail-safe N was 67, suggesting that 67 additional negative studies would be needed to negate the results of our meta-analysis. A much more conservative variant of this method, the Orwin's fail-safe N, assumes that unpublished or future studies are not simply negative but rather in disfavor of NaHCO3. Under the very conservative assumption of a mean OR of 2.7 in unpublished studies (as observed in the included trial with the most extreme result ), eight such trials would be necessary to nullify the overall beneficial effect of NaHCO3.
Need for dialysis
The need for HD was reported in 12 studies (N = 2,011), in five of these, there was no HD event in either group [8, 16, 19, 20, 23]. Overall, 6 out of 934 patients treated with NaHCO3 underwent HD (range 0% to 3.3%) compared with 12 out of the 927 patients treated with NS (range 0% to 10.3%). This difference was not statistically significant (OR 0.53; 95% CI 0.20–1.41, P = 0.20).
Data for mortality were available from seven studies (N = 1,334). In three studies, no death was observed in either group [11, 19, 23]. There were a total of eight deaths in the 886 patients treated with NaHCO3 (range 0% to 1.8%) and 12 in the 666 patients treated with NS (range 0% to 7.3%). The overall-mortality risk was not significantly different between the two treatment groups (OR 0.74; 95% CI 0.29–1.9, P = 0.53).
In this meta-analysis of 17 RCTs including 2,633 patients, pre-procedural hydration with NaHCO3 reduced the incidence of CIN compared with hydration with NS. Our findings thus corroborate and extend the prior meta-analysis in the field. Our findings were based on a larger number of trials, include a much larger patient population and adjusted for publication bias by including multiple unpublished studies.
Although CIN is generally limited to a transient decline of renal function, it can not be regarded as a benign complication. Some degree of residual renal impairment has been reported in as many as 30% of those affected by CIN . In an observational study of patients undergoing percutaneous coronary intervention, dialysis was started in 0.8%; persistent renal failure requiring permanent dialysis developed in 13% of these patients ; in patients with diabetes and severe renal failure the rate of dialysis was even higher . CIN is associated with a prolonged hospital stay and corresponding additional costs [8, 17], and it portends a high morbidity and an increased in-hospital and long-term mortality [39–43]. Acute renal insufficiency leads to increased myocardial oxygen consumption and impaired vascular function in dogs  and it is plausible that similar mechanisms may be applicable in humans.
However, this diminished risk for CIN seems not to translate into a decreased incidence of death or need for HD in this current meta-analysis. A similar phenomenon has also been reported in studies evaluating NAC . Several reasons may account for this disconnection between CIN and need for renal replacement therapy or mortality. The patient population enrolled in these studies was generally young and at low risk of adverse events, and very few studies provide long-term follow-up data. The incidence of mortality and need for HD was low in general. Given such low event rates, even a pooled analysis is underpowered to detect a significant difference. Furthermore, it is possible that the definitions of CIN used in these studies are too sensitive regarding the prediction of adverse outcome. Finally, contrast media may impair tubular creatinine excretion, which could lead to an underestimation of the renal function when using creatinine as a surrogate . Importantly, while not significant statistically, the incidence of both death and need for renal replacement therapy was lower in the NaHCO3 arm.
While the overall results of the meta-analysis and the imputed OR favors use of NaHCO3, possible reasons for heterogeneity must be considered. The study populations and the study settings were rather variable. Stratified analyses revealed differences between NaHCO3 effects in emergency and elective cases as one potential reason for the heterogeneity. Interestingly, the benefit of NaHCO3 was less prominent in patients treated with iso-osmolar contrast than in those treated with other contrast agents. Recent studies suggest that iodixanol may be less nephrotoxic compared with some (but not all) low molecular weight contrast agents and further studies are warranted to assess the interaction between the type of contrast agent used and the hydration strategy. These post-hoc analyses (meta-regressions, subset analyses) must be considered exploratory and hypothesis generating since they are based on a small number of trials and no adjustment for multiple comparisons was made.
The presented overall benefit of NaHCO3 may also be slightly overestimated by the two trials that were stopped early (both because of an overwhelming beneficial effect in the treatment group). Early stopping is controversial and it can lead to an overestimation of a treatment effect . However, the early stopped trials are rather small, and their overall influence therefore limited. Even after exclusion of these two studies, the overall benefit of NaHCO3 persists.
The importance of publication bias in meta-analysis in general and in this field in particular has been highlighted in the past. The overall magnitude of CIN reduction was clearly greater in published studies compared with unpublished studies. The strength of this study is the inclusion of all available unpublished data and therefore represents the most robust analysis in this field so far. However, even after a comprehensive search for, and inclusion of these unpublished studies, formal testing indicates a likelihood of more unpublished data. Based on statistical estimations, the number and overall effect of unpublished data are probably limited. The treatment effect based on imputed estimated unpublished studies still supports superiority of NaHCO3 (OR 0.62; 95% CI 0.40–0.97). The use of NaHCO3 is likely associated with a reduction in the incidence of CIN, which may be somewhat overestimated by unpublished studies.
On the other hand, the inclusion of many unpublished studies to overcome the problem of publication bias, introduces the possibility of including lower-quality data that has not undergone robust peer review. However, these trials have all been presented at scientific meetings, published in an abstract format and have undergone a limited peer-review.
While most randomized data suggest either a lower risk of CIN with NaHCO3 or no difference compared with NS, a large observational study from the Mayo Clinic has raised the possibility of potential harm with this strategy. In a retrospective study of 7,911 patients encompassing 11,516 cases of contrast exposure, the risk of CIN among patients treated with NaHCO3 was significantly increased compared with the untreated group (OR 3.0, P < 0.05) . Only a small proportion of patients (489 out of 7,977) were pre-treated with NaHCO3 and the extreme results of this study in contrast to the randomized data suggest that the conclusions may be driven by unrecognized confounders. It is reassuring that despite multiple trials performed in various countries, none has demonstrated superiority of saline-based hydration and the overall odds of mortality and need for renal replacement therapy albeit exceedingly low overall, are lower in the NaHCO3 arm. The cumulative analysis further supports this conclusion, at no particular time point since the first publication of Merten et al. , the OR pointed towards an inferiority of NaHCO3. However, this also illustrates the fact that the effect of NaHCO3 probably was significantly overestimated at first and the inclusion of the recent studies seems to be leading us closer to a more accurate estimate of effect size.
It remains unclear whether there is a dose effect and whether alkalinization is the underlying beneficial mechanism. Six studies monitored the degree of alkalinization (pH urine or blood) [11, 15, 19, 20, 22, 24]. All but one found a significant increase in pH with exception of Lin et al. , which in fact was the only one among them not to find a benefit of NaHCO3. Therefore, it could be hypothesized that NaHCO3 should be dosed to achieve urinary alkalinization. Promisingly, the study of Tamura et al.  indicates that even a single bolus of NaHCO3 administered just prior to contrast administration may be effective and such a protocol could be easily used in most healthcare settings. The efficacy of this approach, however, needs validation in larger studies before it can be recommended for widespread use.
Our meta-analysis suggested a significant benefit of using NaHCO3-based hydration for prophylaxis of CIN although the magnitude of the benefit may have been overestimated by earlier studies. However, the lack of any study to date showing superiority of saline-based hydration suggests that NaHCO3-based hydration should be considered the optimal hydration in high-risk patients undergoing exposure to iodinated contrast.
randomized controlled trial
Hou SH, Bushinsky DA, Wish JB, Cohen JJ, Harrington JT: Hospital-acquired renal insufficiency: a prospective study. Am J Med. 1983, 74: 243-248. 10.1016/0002-9343(83)90618-6.
Boyden TF, Gurm HS: Does gadolinium-based angiography protect against contrast-induced nephropathy?: a systematic review of the literature. Catheter Cardiovasc Interv. 2008, 71: 687-693. 10.1002/ccd.21459.
Katholi RE, Woods WT, Taylor GJ, Deitrick CL, Womack KA, Katholi CR, McCann WP: Oxygen free radicals and contrast nephropathy. Am J Kidney Dis. 1998, 32: 64-71. 10.1053/ajkd.1998.v32.pm9669426.
Russo D, Minutolo R, Cianciaruso B, Memoli B, Conte G, De Nicola L: Early effects of contrast media on renal hemodynamics and tubular function in chronic renal failure. J Am Soc Nephrol. 1995, 6: 1451-1458.
Atkins J: Effect of sodium bicarbonate preloading on ischemic renal failure. Nephron. 1986, 44: 70-74. 10.1159/000183915.
Hogan SE, L'Allier P, Chetcuti S, Grossman PM, Nallamothu BK, Duvernoy C, Bates E, Moscucci M, Gurm HS: Current role of sodium bicarbonate-based preprocedural hydration for the prevention of contrast-induced acute kidney injury: a meta-analysis. Am Heart J. 2008, 156: 414-421. 10.1016/j.ahj.2008.05.014.
Navaneethan SD, Singh S, Appasamy S, Wing RE, Sehgal AR: Sodium bicarbonate therapy for prevention of contrast-induced nephropathy: a systematic review and meta-analysis. Am J Kidney Dis. 2009, 53: 617-627. 10.1053/j.ajkd.2008.08.033.
Adolph E, Holdt-Lehmann B, Chatterjee T, Paschka S, Prott A, Schneider H, Koerber T, Ince H, Steiner M, Nienaber CA, Schuff-Werner P: Renal Insufficiency Following Radiocontrast Exposure Trial (REINFORCE): a randomized comparison of sodium bicarbonate versus sodium chloride hydration for the prevention of contrast-induced nephropathy. Coron Artery Dis. 2008, 19: 413-419.
Maioli M, Toso A, Leoncini M, Gallopin M, Tedeschi D, Micheletti C, Bellandi F: Sodium bicarbonate versus saline for the prevention of contrast-induced nephropathy in patients with renal dysfunction undergoing coronary angiography or intervention. J Am Coll Cardiol. 2008, 52: 599-604. 10.1016/j.jacc.2008.05.026.
Malpica EM, Gonzalez Queseda C, Delgadillo Rodriguez H, Uribe J: Prevention of contrast induced nephropathy using sodium bicarbonate in moderate to very high risk patients (a randomized clinical trial) [abstract]. Paper presented at Transcatheter Cardiovascular Therapeutics Meeting: Washington DC. 2008
Tamura A, Miyamoto K, Naono S, Kawano Y, Kotoku M, Watanabe T, Kadota J: A single bolus intravenous administration of sodium bicarbonate is effective in the prevention of contrast-induced nephropathy in patients with renal insufficiency undergoing diagnostic coronary arteriography or elective percutaneous coronary intervention [abstract]. Paper presented at American Heart Association; New Orleans, Louisiana. 2008
From AM, Bartholmai BJ, Williams AW, Cha SS, Pflueger A, McDonald FS: Sodium bicarbonate is associated with an increased incidence of contrast nephropathy: a retrospective cohort study of 7977 patients at Mayo Clinic. Clin J Am Soc Nephrol. 2008, 3: 10-18. 10.2215/CJN.03100707.
Schmidt P, Pang D, Nykamp D, Knowlton G, Jia H: N-acetylcysteine and sodium bicarbonate versus N-acetylcysteine and standard hydration for the prevention of radiocontrast-induced nephropathy following coronary angiography. Ann Pharmacother. 2007, 41: 46-50.
Shavit L, Korenfeld R, Butnaru A, Slotki I: Sodium bicarbonate compared to sodium chloride and oral N-acetylcysteine for the prevention of contrast induced nephropathy in patients with advanced chronic kidney disease [abstract]. Paper presented at American Society of Nephrology Meeting (abstract SA-PO2983): Philadelphia, PA. 2008
Briguori C, Airoldi F, D'Andrea D, Bonizzoni E, Morici N, Focaccio A, Michev I, Montorfano M, Ricciardelli B, Colombo A: Renal insufficiency following contrast media administration trial (REMEDIAL). Circulation. 2007, 115: 1211-1217.
Heguilen R, Liste R, Rosende G, Ortenberg M, Quevedo A, Payaslian M: Prevention of contrast-induced nephropathy: volume expansion, N-acetylcysteine or both? Results from a pilot study [abstract]. Nephrol Dial Transplant. 2007, 22: vi.
Hengel C, Chase A, Klinke W, Fretz E, Della Siega A, Williams M, Kinloch R, Mildenberger R, Hilton J: Bicarbonate for coronary angiographic renal protection (BICAR) trial [abstract]. Paper presented at Canadian Cardiovascular Congress: Vancouver, Canada. 2006
Kim G, Kim K, Shin J, Lee C, Kang C: Hydration with sodium bicarbonate for the prevention of radio contrast-induced nephropathy [abstract]. Nephrol Dial Transplant. 2007, 22: vi-10.1093/ndt/gfm386. 49 (Suppl 6: abstract FP096).
Lin M, Sabeti M, Iskander E, Malhotra N, Pham P, Pham P: Prevention of contrast nephropathy with sodium bicarbonate [abstract]. Paper presented at American Society of Nephrology Meeting (abstract SA-PO2986): Philadelphia, PA. 2008
Merten GJ, Burgess WP, Gray LV, Holleman JH, Roush TS, Kowalchuk GJ, Bersin RM, Van Moore A, Simonton CA, Rittase RA, Norton HJ, Kennedy TP: Prevention of contrast-induced nephropathy with sodium bicarbonate. JAMA. 2004, 291: 2328-2334. 10.1001/jama.291.19.2328.
Saidin R, Zainudin S, Kong N, Maskon O, Saaidin N, Shah S: Intravenous sodium bicarbonate versus normal saline infusion as prophylaxis against contrast nephropathy in patients with chronic kidney disease undergoing coronary angiography or angioplasty [abstract]. J Am Soc Nephrol. 2006, 17: 766A.
Recio-Mayoral A, Chaparro M, Prado B, Cózar R, Méndez I, Banerjee D, Kaski JC, Cubero J, Cruz JM: The reno-protective effect of hydration with sodium bicarbonate plus N-acetylcysteine in patients undergoing emergency percutaneous coronary intervention (the RENO study). J Am Coll Cardiol. 2007, 49: 1283-1288. 10.1016/j.jacc.2006.11.034.
Chen H, Wu H, He Q, Chen H: Comparison of sodium bicarbonate and sodium chloride as strategies for preventing contrast nephropathy [abstract]. J Am Soc Nephrol. 2007, 18: 817A-10.1681/ASN.2006091021. (abstract SU-PO1046).
Masuda M, Yamada T, Mine T, Morita T, Tamaki S, Tsukamoto Y, Okuda K, Iwasaki Y, Hori M, Fukunami M: Comparison of usefulness of sodium bicarbonate versus sodium chloride to prevent contrast-induced nephropathy in patients undergoing an emergent coronary procedure. Am J Cardiol. 2007, 100: 781-786. 10.1016/j.amjcard.2007.03.098.
Ozcan EE, Guneri S, Akdeniz B, Akyildiz IZ, Senaslan O, Baris N, Aslan O, Badak O: Sodium bicarbonate, N-acetylcysteine, and saline for prevention of radiocontrast-induced nephropathy. A comparison of 3 regimens for protecting contrast-induced nephropathy in patients undergoing coronary procedures. A single-center prospective controlled trial. Am Heart J. 2007, 154: 539-544. 10.1016/j.ahj.2007.05.012.
Shaikh F, Mortada ME, Maddikunta R, Museitif R, Haddadian B, Dochee J, Nazir A, Qureshi J, Wallach J, Solias J, Tumuluri R, Allaqaband S, Bajwa T: Prospective, randomized comparison of hydration with sodium bicarbonate versus normal saline with or without N-acetylcysteine for the prevention of contrast-induced nephropathy in high-risk patients [abstract]. Paper presented at Transcatheter Cardiovascular Therapeutics Meeting: Washington DC. 2007
Brar SS, Shen AY, Jorgensen MB, Kotlewski A, Aharonian VJ, Desai N, Ree M, Shah AI, Burchette RJ: Sodium bicarbonate vs sodium chloride for the prevention of contrast medium-induced nephropathy in patients undergoing coronary angiography: a randomized trial. JAMA. 2008, 300: 1038-1046. 10.1001/jama.300.9.1038.
Juni P, Witschi A, Bloch R, Egger M: The hazards of scoring the quality of clinical trials for meta-analysis. JAMA. 1999, 282: 1054-1060. 10.1001/jama.282.11.1054.
Sankey S, Weissfeld L, Fine M, Kapoor W: An assessment of the use of the continuity correction for sparse data in metanalysis. Communications in Statistics: Simulation and Computation. 1996, 25: 1031-1056. 10.1080/03610919608813357.
Begg C, Mazumdar M: Operating characteristics of a rank correlation test for publication bias. Biometrics. 1994, 50: 1088-1101. 10.2307/2533446.
Egger M, Davey SG, Schneider M, Minder C: Bias in meta-analysis detected by a simple, graphical test. BMJ. 1997, 315: 629-634.
Orwin R: A fail-safe N for effect size in meta-analysis. J Ed Stat. 1983, 8: 157-159.
Rosenberg M: The file-drawer problem revisited: a general weighted method for calculating fail-safe numbers in meta-analysis. Evolution. 2005, 59: 464-468.
Duval S, Tweedie R: A simple funnel-plot-based method of testing and adjusting for publication bias in meta-analysis. Biometrics. 2000, 56: 455-463. 10.1111/j.0006-341X.2000.00455.x.
Bax L, Yu LM, Ikeda N, Tsuruta H, Moons KG: Development and validation of MIX: comprehensive free software for meta-analysis of causal research data. BMC Med Res Methodol. 2006, 6: 50-10.1186/1471-2288-6-50.
Madyoon H, Croushore L, Weaver D, Mathur V: Use of fenoldopam to prevent radiocontrast nephropathy in high-risk patients. Catheter Cardiovasc Interv. 2001, 53: 341-345. 10.1002/ccd.1178.
McCullough P, Wolyn R, Rocher L, Levin RN, O'Neill WW: Acute renal failure after coronary intervention: incidence, risk factors, and relationship to mortality. Am J Med. 1997, 103: 368-375. 10.1016/S0002-9343(97)00150-2.
Manske CL, Sprafka JM, Strony JT, Wang Y: Contrast nephropathy in azotemic diabetic patients undergoing coronary angiography. Am J Med. 1990, 89: 615-620. 10.1016/0002-9343(90)90180-L.
Gupta R, Gurm HS, Bhatt DL, Chew DP, Ellis SG: Renal failure after percutaneous coronary intervention is associated with high mortality. Catheter Cardiovasc Interv. 2005, 64: 442-448. 10.1002/ccd.20316.
From AM, Bartholmai BJ, Williams AW, Cha SS, McDonald FS: Mortality associated with nephropathy after radiographic contrast exposure. Mayo Clin Proc. 2008, 83: 1095-1100. 10.4065/83.10.1095.
Nash K, Hafeez A, Hou S: Hospital-acquired renal insufficiency. Am J Kidney Dis. 2002, 39: 930-936. 10.1053/ajkd.2002.32766.
Laskey W, Ed: Contrast-induced nephropathy: clinical insights and practical guidance – a report from the CIN Consensus Working Panel. Am J Cardiol. 2006, 98: 1-78. 10.1016/j.amjcard.2006.03.001.
Roghi A, Savonitto S, Cavallini C, Arraiz G, Angoli L, Castriota F, Bernardi G, Sansa M, De Servi S, Pitscheider W, Danzi GB, Reimers B, Klugmann S, Zaninotto M, Ardissino D, Atherosclerosis, Thrombosis and Vascular Biology Study Group and the Italian Society for Invasive Cardiology Investigators: Impact of acute renal failure following percutaneous coronary intervention on long-term mortality. J Cardiovasc Med (Hagerstown). 2008, 9: 375-381.
Kingma JG, Vincent C, Rouleau JR, Kingma I: Influence of acute renal failure on coronary vasoregulation in dogs. J Am Soc Nephrol. 2006, 17: 1316-1324. 10.1681/ASN.2005101084.
Nallamothu B, Shojania K, Saint S, Hofer T, Humes D, Moscucci M, Bates E: Is acetylcysteine effective in preventing contrast-related nephropathy? A meta-analysis. Am J Med. 2004, 117: 938-947. 10.1016/j.amjmed.2004.06.046.
Crawford B: Depression of the exogenous creatinine/inulin or thiosulfate clearance ratios in man by diodrast and p-aminohippuric acid. J Clin Invest. 1948, 27: 171-175. 10.1172/JCI101931.
Montori VM, Devereaux PJ, Adhikari NK, Burns KE, Eggert CH, Briel M, Lacchetti C, Leung TW, Darling E, Bryant DM, Bucher HC, Schunemann HJ, Meade MO, Cook DJ, Erwin PJ, Sood A, Sood R, Lo B, Thompson CA, Zhou Q, Mills E, Guyatt GH: Randomized trials stopped early for benefit: a systematic review. JAMA. 2005, 294: 2203-2209. 10.1001/jama.294.17.2203.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1741-7015/7/23/prepub
We are especially grateful to Whitney Townsend, Librarian, Taubman Medical Library, University of Michigan, for her valuable inputs during the literature search. We thank Dr M. Lin and Dr Phuong-Chi Pham, Olive View-UCLA Medical Center, Sylmar, CA, USA, and Dr Lina Shaik and Dr Itzchak Slotki, Shaare Zedek Medical Center, Jerusalem, Israel, for providing important information on their studies.
The authors declare that they have no competing interests.
PM was responsible for the conception and design, acquisition of data, analysis and interpretation of data, and drafting of the manuscript. DTK and AT revised the manuscript critically for important intellectual content. UT was responsible for the analysis and interpretation of data. HSG was responsible for the conception and design, acquisition, analysis and interpretation of data, and revising the manuscript critically for important intellectual content. All authors approved the final version of the manuscript and had full access to all of the data in the study.