Kidney Res Clin Pract > Volume 40(3); 2021 > Article
Jahangir, Sahra, Niazi, Siddiqui, Anwar, Jahangir, and El-Charabaty: Comparison of normal saline solution with low-chloride solutions in renal transplants: a meta-analysis

Abstract

Background

Normal saline solution (NSS) has been the fluid of choice for renal transplant patients, but it can lead to hyperchloremic acidosis and hyperkalemia. This study was performed to compare the safety profile of low-chloride solutions with that of NSS in renal transplant patients.

Methods

We conducted a systemic review search on PubMed, Embase, and the Central Cochrane Registry. Randomized clinical trials (RCTs) and matched cohort studies involving NSS as the control arm and low-chloride solutions as an intervention arm were chosen. The standardized mean difference for continuous variables, the odds ratio (OR) for discrete variables, and a 95% confidence interval (CI) for effect sizes were used. A p-value of <0.05 was considered statistically significant. Analysis was performed using a random-effects model irrespective of heterogeneity, which was evaluated using I2 statistics.

Results

Nine RCTs and one cohort study with a total of 726 patients were included. After transplantation, serum potassium was significantly lower in the low-chloride group (standardized mean difference compared to NSS group, –0.38 mEq/L; 95% CI, –0.66 to –0.11; p = 0.007). Similarly, postoperative chloride was lower in the low-chloride group (–2.41 mEq/L [–3.34 to –1.48], p < 0.001). No statistically significance was observed in delayed graft function (OR, 0.98 [0.56–1.69], p = 0.93), day 3 creatinine (–0.14 mg/dL [–0.46 to 0.18], p = 0.38), or day 7 urine output (–0.08 L [–0.29 to 0.12], p = 0.43).

Conclusion

Use of NSS during renal transplant leads to increased incidence of hyperchloremic acidosis with subsequent hyperkalemia, but clinical significance in the form of delayed graft function or postoperative creatinine remains comparable to that of low-chloride solutions.

Introduction

End-stage renal disease is a significant cause of global morbidity and mortality, with kidney transplantation being the treatment of choice as it offers substantial survival benefits over dialysis.
The total number of kidney transplants is increasing steadily every year. According to the data obtained from Organ Procurement and Transplantation Network government website, 22,393 patients received a renal transplant in 2018. According to the annual report 2020 published by the United States Renal Data System, 1-year posttransplant graft survival improved to 93% in deceased donor transplant recipients compared to 96.9% in living donor transplant recipients. The limited availability of donor viscera necessitates measures to improve graft function and survivability.
Normal saline solution (NSS) is the most used perioperative intravenous fluid during kidney transplant due to theoretically reduced risk for perioperative hyperkalemia [1]. It is postulated that fluids like Ringer’s lactate possess a high potassium content and can cause hyperkalemia postoperatively [2,3]. There is some evidence that suggests that higher chloride content in NSS can cause hyperchloremic metabolic acidosis and subsequent hyperkalemia as an effect of acidosis on potassium homeostasis [4].
In comparison, balanced chloride solutions are less likely to cause hyperkalemia by virtue of their low-chloride content. This meta-analysis will determine if we can extrapolate these electrolyte and blood pH changes associated with NSS to renal transplant surgeries. Hyperkalemia is an indication for dialysis posttransplant and can lead to decreased cardiovascular stability of the transplant recipient. Therefore, it is hypothesized that normal saline will increase the risk of delayed graft function, defined as the need for dialysis within 1 week of renal transplantation or not observing a 20% reduction in serum creatinine within 72 hours [5].
The purpose of this review is to compare NSS to balanced crystalloid solutions and the incidence of postoperative delayed graft function, acidemia, and hyperkalemia in renal transplant patients. With the last being in 2016, previous reviews support that NSS is associated with more hyperchloremic metabolic acidosis than are balanced electrolyte solutions, but with uncertain clinical significance [6]. However, three randomized clinical trials (RCTs) on the topic have been performed since 2016, requiring their inclusion for a higher-powered review. We aim to increase the study power by including recently published trials and provide a more comprehensive guideline for physicians overseeing the care of renal transplant patients.

Methods

The databases accessed were the Cochrane Central Registry of Clinical Trials, Embase, and PubMed. The search terms used were renal transplant, sodium bicarbonate, normal saline solution, and Ringer’s lactate. The deadline for publication was set as December 20, 2020. The data were extracted, and the manuscript was reviewed by the Research Department and Ethics Committee. No experimental interventions were performed, and it did not require any specification of guidelines, legislations, or permissions.

Inclusion and exclusion criteria

Included papers had the following characteristics.
(1) Randomized control trials or matched retrospective cohort studies comparing NSS against low-chloride solutions in renal transplant patients
(2) Patients older than 18 years
(3) Available in English without restrictions of date or status of publication
Papers that did not meet the above criteria were excluded.

Trial selection and evaluation

Three authors independently reviewed all articles and abstracts and excluded irrelevant articles. The risk of bias for selected papers was assessed using the Cochrane collaborative tool and was classified into high, uncertain, and low.

Data extraction

Information was extracted using a prespecified extraction table from analysis of text and tables, and a second author reviewed the information to ensure accuracy. The extracted data were the number of patients, delayed graft function, serum creatinine at day 3 (mg/dL), urine output at day 7 (L), postoperative chloride (mEq/L), postoperative potassium (mEq/L), postoperative blood pH, postoperative base excess (mEq/L), and postoperative bicarbonate (mEq/L).

Statistical analysis

The meta-analysis was performed using the Comprehensive Meta-Analysis software version 3 (Biostat Inc., Englewood, NJ, USA). We calculated the standardized mean difference in continuous variables for treatment effect measurements, while the odds ratio (OR) was calculated for discrete variables. Standard errors were calculated using a 95% confidence interval (CI), and a p-value of 0.05 was used for determining statistical significance. For consistency in analysis, a random-effects model was used irrespective of heterogeneity. Heterogeneity was evaluated using the I2 statistic. Heterogeneity less than 40 was considered low, 40 to 60 moderate, and above 60 high. Continuous variables reported as medians were assumed to be equivalent to the mean, and standard deviation (SD) estimation was obtained by dividing the interquartile difference by 1.35.

Results

Literature search

A total of 3,434 articles was identified in the initial search. After removal of duplicates, we filtered 3,217 articles. The first screening excluded 3,116 articles. Full texts of 111 articles were analyzed. Twenty-eight articles were excluded as review articles and one was not available in English. Ten articles were pediatric studies. Twenty-five were not interventional studies, 18 did not have relevant interventions, five were case reports, three were protocol papers, and 11 were miscellaneous (letter to editors and addendums) (Fig. 1). We included nine randomized control trials and one retrospective cohort with a total of 726 patients. The main characteristics are provided in Table 1 [7-16].

Risk of bias

The results of the risk of bias are shown in Fig. 2, 3.

Results of quantitative analysis

The results of quantitative analysis are summarized in Fig. 4 to 6.

Delayed graft function

Five studies reported the incidence of delayed graft function. The difference in delayed graft function between the two groups was not statistically significant, with an OR of 0.98 (95% CI, 0.56–1.69; p = 0.93, I2 = 0).

Day 3 creatinine

Serum creatinine measured at day three after surgery was reported in seven studies and was not statistically significant, with a standardized mean difference of –0.14 (95% CI, –0.46 to 0.18; p = 0.38, I2 = 71.525).

Postoperative potassium

Postoperative potassium was reported in six studies and was significantly lower in the low-chloride group, with a standardized mean difference of –0.38 (95% CI, –0.66 to –0.11; p = 0.007, I2 = 48.809).

Postoperative chloride

Seven studies reported postoperative chloride and showed significantly lower level in the low-chloride group, with a standardized mean difference of –2.41 (95% CI, –3.34 to –1.48; p < 0.001, I2 = 95.296).

Postoperative bicarbonate

Five studies reported postoperative bicarbonate and significantly higher bicarbonate in the low-chloride group, with a standardized mean difference of 0.71 (95% CI, 0.34–1.08; p < 0.001, I2 = 62.591).

Day 7 urine output

The mean difference of urine output at day 7 after surgery was not statistically significant, with a standardized mean difference of –0.08 (95% CI, –0.29 to 0.12; p = 0.43, I2 = 0).

Postoperative blood pH

Four studies reported postoperative blood pH and showed a statistically higher blood pH in the low-chloride group, with a standardized mean difference of 0.84 (95% CI, 0.23–1.46; p = 0.007, I2 = 82.146).

Postoperative base excess

Five studies reported postoperative base excess and significant negative base excess in the normal saline group, with a standardized mean difference of 0.99 (95% CI, 0.42–1.56; p = 0.001, I2 = 87.321).

Subgroup analysis

We performed subgroup analysis for delayed graft function, day 3 creatinine, and postoperative potassium level in studies that only included living donors.
The OR for delayed graft function remained not statistically significant (0.83; 95% CI, 0.24–2.90; p = 0.77). Similarly, the OR of day three creatinine was not statistically significant with a random-effects model (–0.21; 95% CI, –0.62 to 0.20). The OR for postoperative potassium level remained significantly lower in the low-chloride group (–0.44; 95% CI, –0.76 to –0.13; p = 0.006).

Summary of results

Low-chloride solutions were associated with lower chloride and potassium levels, less negative base excess, and higher blood pH postoperatively without significant difference in postoperative delayed graft function, day 3 creatinine, or urine output at day 7.

Discussion

Intraoperative fluid management during kidney transplants has been a topic of discussion for the past decade. Transplant physicians have extensively debated the fluid of choice based on composition, like chloride or potassium concentration, blood pH, and tonicity. Since low-chloride solutions (like lactated Ringer’s) have a higher concentration of potassium that can theoretically cause hyperkalemia, NSS is considered the fluid of choice during renal transplant [7]. Nevertheless, due to its high chloride concentration, NSS can cause hyperchloremic metabolic acidosis, leading to compensatory hyperkalemia in patients during the initial posttransplant period [8,17]. Several trials have exhibited hyperchloremia with adverse outcomes in kidney transplant patients [1820].
It is postulated that supraphysiologic level of chloride releases thromboxane and augmented responses to renal vasoconstrictors [21]. Furthermore, increased chloride delivery to the macula densa leads to tubuloglomerular feedback resulting in afferent arteriolar vasoconstriction, mesangial contractions, and decreased glomerular filtration rate [22].
The debate about ideal fluid during kidney transplants continues. Colloids usually are not used because they are associated with several adverse effects, including renal failure [23,24]. Our study looked for factors like delayed graft function or clinically significant hyperkalemia in patients who received NSS versus low-chloride solutions. The last study performed on choice of fluids during renal transplant is the Cochrane review published in 2016, with 6 RCTs and 477 participants [7]. A previous meta-analysis published in the Columbian Journal of Anesthesiology (2015) included four RCTs with a total of 267 participants (n = 267) [25]. Since 2016, there have been three more RCTs, necessitating inclusion of these studies to increase population size and unmask any missed differences. Our study included nine RCTs and one retrospective cohort study with a total of 276 total participants (n = 276).
Our study shows that low-chloride solutions are better than NSS when transfused during renal transplant. We noticed increased risk of hyperchloremia and base deficit (both of which lead to metabolic acidosis) with NSS. The high chloride leads to loss of bicarbonate and ultimately acidosis. Potassium acts as a buffer to acidosis, resulting in hyperkalemia.
In terms of acid-base balance, the blood pH was significantly lower in the NSS group (OR, 0.84; 95% CI, 0.23–1.46; p = 0.007, I2 = 82.146). The low-chloride solution group showed increased postoperative serum bicarbonate and blood pH levels. A new significant finding compared to previous meta-analyses like Trujillo-Zea et al. [25] and the Cochrane review [6] is postoperative hyperkalemia (mean difference, –0.38; 95% CI, –0.66 to –0.11; p = 0.007, I2 = 48.809) in the NSS group when analyzed under a random-effects model. The postoperative potassium was higher in the NSS group in all studies except for O’Malley et al. [7], likely because the baseline potassium level was higher in the low-chloride group (4.5 ± 0.5 compared to 4.2 ± 0.7 in the NSS group).
For the patients receiving treatment for acidosis after transplantation, the trend seemed inclined toward NSS in all the studies except Weinberg et al. Overall, the difference was not statistically significant likely due to the small number of patients.
We observed high heterogeneity in postoperative blood pH, chloride, bicarbonate, and base excess. The heterogeneity can be attributed to concurrent interventions such as in Fathi et al. [14] where all the patients were given 50 ml/kg of normal saline. For example, when Fathi et al. [14] was excluded from the analysis for blood pH, the standardized mean difference increased to 1.14 (95% CI, 0.85–1.42), reducing I2 to 7.524. Similarly, the bicarbonate standardized mean difference increased to 0.85 (95% CI, 0.56–1.14), reducing I2 to 29.683. Additionally, a variable amount of fluid administration in the pre- and postoperative periods also added to the study heterogeneity.
There was no significant difference in delayed graft function, creatinine at day three, or urine output on postoperative day 7, and heterogeneity was small. This finding is important because, in the past, use of low-chloride solutions like Ringer’s lactate has been discouraged due to risk of postoperative hyperkalemia and renal injury. In this study, there was no difference in postoperative urine output, blood urea nitrogen, or creatinine levels with fluid use, indicating that low-chloride solutions are as safe as if not better than NSS during kidney transplant surgery.
The study’s major strengths include a larger patient population analyzed than earlier reviews and comprehensive analysis of multiple parameters. This study revealed a significant finding in contrast to previous meta-analyses like Trujillo-Zea et al. [25] and the Cochrane review [6]. Postoperative hyperkalemia (standardized mean difference, –0.38; 95% CI, –0.66 to –0.11; p = 0.007, I2 = 48.809) was seen in the NSS group when analyzed under a random-effects model.
Being a meta-analysis, this study remains a retrospective chart review and creates the possibility for biases. Smaller numbers of trials and people enrolled lead to publication bias. The difference in composition of low-chloride solutions creates potential bias. Although there is a difference in chloride concentration in these solutions among studies, they have less chloride than NSS. We excluded colloid fluids produced in normal saline as they have the same chloride content as NSS (e.g., hydroxyethyl starches in normal saline) to minimize the bias. However, we aimed to prove that using these fluids with lower-chloride solution than NSS would reduce the risk of hyperchloremia to result in less hyperkalemia and acidosis, as seen in the results. Another significant limitation is the different follow-up times at which the readings were obtained. We attempted to tackle this by choosing readings closest to each other in timing to minimize the bias in the results.
Overall, we made our best effort to search for all published studies, randomize them, and complete data extraction and analysis. These trials are based on intraoperative use of fluids. Transplant patients undergo a large amount of intravenous fluid infusion at 48 to 72 hours after surgery. Postoperative values for creatinine, potassium, bicarbonate, and blood pH vary with type of fluid used during this postoperative period, and further studies are needed to take this into account.
In conclusion, low-chloride solutions are a safe alternative to NSSs in renal transplant patients, and their use is associated with lower potassium, chloride, and higher blood pH postoperatively. They could be the fluids of choice in patients with high risk of hyperkalemia and acidosis during surgery.

Notes

Conflicts of interest

All authors have no conflicts of interest to declare.

Authors’ contributions

Investigation: SS, Abdullah Jahangir, MRKN, FSS, MYA, Ahmad Jahangir

Data curation: Abdullah Jahangir, EJE

Writing–original draft: SS, Abdullah Jahangir, MRKN, FSS, MYA, Ahmad Jahangir

Writing–review & editing: Abdullah Jahangir, EJE

All authors read and approved the final manuscript.

Figure 1.
PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) chart for the selection of the studies.
j-krcp-21-027f1.jpg
Figure 2.
Results of the risk of biases in the included studies.
j-krcp-21-027f2.jpg
Figure 3.

Results of the risk of biases in the included studies.

j-krcp-21-027f3.jpg
Figure 4.

Results of the risk of biases in the included studies. Quantitative results analysis for delayed graft function and day 3 serum creatinine (mg/dL).

(A) Delayed graft function. (B) Day 3 creatinine. CI, confidence interval; NSS, normal saline solution; RL, Ringer's lactate; PL, plasmalyte.
j-krcp-21-027f4.jpg
Figure 5.

Quantitative results analysis for postoperative potassium, postoperative bicarbonate, and postoperative chloride.

(A) Postoperative potassium (mEq/L). (B) Postoperative bicarbonate (mEq/L). (C) Postoperative chloride (mEq/L).
CI, confidence interval; NSS, normal saline solution; RL, Ringer's lactate; PL, plasmalyte.
j-krcp-21-027f5.jpg
Figure 6.

Quantitative results analysis for day 7 urine output, postoperative blood pH, and postoperative base excess.

(A) Day 7 urine output (L). (B) Postoperative blood pH. (C) Postoperative base excess. CI, confidence interval; NSS, normal saline solution; RL, Ringer's lactate; PL, plasmalyte.
j-krcp-21-027f6.jpg
Table 1.
The main characteristics of Randomized controlled trials (RCTs) included
Study Year Study type Donor type No. of participants Exclusion Intervention Outcome Cointervention
O’Malley et al. [7] 2005 RCT Living or deceased 51 <18 yr, belief preventing the use of blood products, K > 5.5 presurgery RL (n = 25) vs. NSS (n = 26) Serum Cr at postoperative day 3, Cr at day 7 and 6 mo, K and acid-base balance, urine output at 4 and 48 hr Immunosuppression: steroids, calcineurin, and mycophenolate or sirolimus
Routine radial artery catheter and CV catheter discretional
Hadimioglu et al. [8] 2008 RCT Living 90 Severe CVD, liver failure, DM, K > 5.5 presurgery RL (n = 30) vs. NSS (n = 30) vs. plasmalyte (n = 30) Daily urine volume, serum Cr at day 3 after surgery, blood pH, bicarbonate, and K after surgery. Cr, BUN, chloride, urinary output, and Cr clearance at days 1, 2, 3, and 7 after surgery, serum K at the end of surgery, blood pH at the end of surgery Immunosuppression: steroids, cyclosporine, and mycophenolate
Khajavi et al. [9] 2008 RCT Living 52 Serum K > 6 presurgery RL (n = 26) vs. NSS (n = 26) Serum K at the end of surgery, blood pH at the end of surgery, Cr at day 3, urine output at 4 hr Immunosuppression: steroids, cyclosporine, and mycophenolate
Heparin 5,000 IU IV
Routine radial artery catheter and CV catheter
Maintenance fluids for CVP of 10–15 mmHg
Modi et al. [10] 2012 RCT Living 74 Severe CVD, liver failure, DM, K > 5.5 presurgery RL (n = 37) vs. NSS (n = 37) Intraoperative and day 1 urine output, serum Cr day 1 after surgery, change in blood pH, intra- and postoperative bicarbonate and K Immunosuppression: steroids
Mannitol, furosemide
Maintain CVP 12–15 mmHg
Kim et al. [11] 2013 RCT Living 60 Severe CVD, severe respiratory disease Plasmalyte (n = 30) vs. NSS (n = 30) blood pH, PaCO2, bicarbonate, sodium, K, chloride lactate, phosphate, and albumin during surgery, serum chloride, Cr, and urine output on postoperative days 1, 2, and 7 Immunosuppression: basiliximab, steroids, calcineurin inhibitor, and mycophenolate or mizoribine
Furosemide
Maintain CVP 12–16 mmHg
Potura et al. [12] 2014 RCT Deceased 150 Age < 18 yr, serum K > 5.5 presurgery Acetate buffered (n = 74) vs. NSS (n = 76) Serum Cr, BUN, urine output on days 1, 3, 7, incidence of hyperkalemia, blood pH, standard BE, chloride, and K during surgery and postoperative surveillance Immunosuppression: not mentioned
Calcium gluconate, insulin, and glucose for hyperkalemia with ECG changes
Weinberg et al. [13] 2017 RCT Deceased 49 Age < 18 yr, serum K > 6 presurgery
CLD (AST/ALT > 1.5× normal)
Plasmalyte (n = 24) vs. NSS (n = 25) Hyperkalemia within 48 hr, hyperkalemia during hospital admission, treatment for hyperkalemia, the requirement for postoperative dialysis, delayed graft function, postoperative complications, and hospital length of stay Immunosuppression: steroids, tacrolimus, mycophenolate, and basiliximab
Furosemide, insulin + glucose for hyperkalemia, no CVP used
Fathi et al. [14] 2018 RCT Living 40 Age < 18 or > 70 yr, advanced CVD, blood pH less than 7.15, temperature < 35°C and > 38.5°C presurgery
Cancer or using immunomodulators
Sodium bicarbonate (n = 20) vs. NSS (n = 20) Acidosis (BE, HCO3-, PCO2, and blood pH), IL-2, IL-10, IFN -, BUN, urine volume, and Cr Immunosuppression: not mentioned
Mannitol and Lasix
Right IJ CVP 10–12 mmHg
Radial artery catheter
Arslantas et al. [15] 2019 Retrospective cohort study design Living 60 Age < 17 or > 67 yr Balanced crystalloids (n = 30) vs. NSS (n = 30) Hyperchloremia and hyperkalemia within 24 hr after surgery, serum Cr at preoperative and within 5 days after transplantation, the incidence of acute rejection episodes, graft failure, length of stay at the hospital, and mortality
Pourfakhr et al. [16] 2020 RCT Deceased 100 K > 5.5 presurgery, COPD, CHF (EF < 30%), BE ≤ –15 mEq/L, bicarbonate ≤ 10 mEq/L, blood pH ≤ 7.15, CLD Half saline bicarbonate (n = 50) vs. NSS (n = 50) Cr at days 1, 3, 5, 7, urine output at 6 and 24 hr, BE, sodium, and chloride Immunosuppression: antithymocyte, globulin infusion presurgery
Radial artery catheter
IJ Catheter

BE, base excess; BUN, blood urea nitrogen; CHF, congestive heart failure; CLD, chronic liver disease; COPD, chronic obstructive pulmonary disease; Cr, serum creatinine (mg/dL); CV, central venous; CVD, cardiovascular disease; CVP, central venous pressure; DM, diabetes mellitus; ECG, electrocardiography; EF, ejection fraction; IFN, interferon; IJ, internal jugular (vein); IL, interleukin; IV, intravenous; K, serum potassium (mEq/L); LFT, liver function test; NSS, normal saline solution; RL, Ringer’s lactate.

References

1. O’Malley CM, Frumento RJ, Hardy MA, et al. A randomized, double-blind comparison of lactated Ringer’s solution and 0.9% NaCl during renal transplantation. Anesth Analg 2005;100:1518–1524.
crossref pmid
2. Belani KG, Palahniuk RJ. Kidney transplantation. Int Anesthesiol Clin 1991;29:17–39.
crossref pmid
3. Murphy BA. Anesthesiologist’s manual of surgical procedures, 3rd ed. Anesth Analg 2004;99:314.
crossref
4. Wilkes NJ, Woolf R, Mutch M, et al. The effects of balanced versus saline-based hetastarch and crystalloid solutions on acid-base and electrolyte status and gastric mucosal perfusion in elderly surgical patients. Anesth Analg 2001;93:811–816.
crossref pmid
5. Yarlagadda SG, Coca SG, Garg AX, et al. Marked variation in the definition and diagnosis of delayed graft function: a systematic review. Nephrol Dial Transplant 2008;23:2995–3003.
crossref pmid pmc
6. Wan S, Roberts MA, Mount P. Normal saline versus lower-chloride solutions for kidney transplantation. Cochrane Database Syst Rev 2016;(8):CD010741.
crossref pmid pmc
7. O’Malley CM, Frumento RJ, Bennett-Guerrero E. Intravenous fluid therapy in renal transplant recipients: results of a US survey. Transplant Proc 2002;34:3142–3145.
crossref pmid
8. Hadimioglu N, Saadawy I, Saglam T, Ertug Z, Dinckan A. The effect of different crystalloid solutions on acid-base balance and early kidney function after kidney transplantation. Anesth Analg 2008;107:264–269.
crossref pmid
9. Khajavi MR, Etezadi F, Moharari RS, et al. Effects of normal saline vs. lactated ringer\'s during renal transplantation. Ren Fail 2008;30:535–539.
crossref pmid
10. Modi MP, Vora KS, Parikh GP, Shah VR. A comparative study of impact of infusion of Ringer\'s lactate solution versus normal saline on acid-base balance and serum electrolytes during live related renal transplantation. Saudi J Kidney Dis Transpl 2012;23:135–137.
pmid
11. Kim SY, Huh KH, Lee JR, Kim SH, Jeong SH, Choi YS. Comparison of the effects of normal saline versus plasmalyte on acid-base balance during living donor kidney transplantation using the Stewart and base excess methods. Transplant Proc 2013;45:2191–2196.
crossref pmid
12. Potura E, Lindner G, Biesenbach P, et al. An acetate-buffered balanced crystalloid versus 0.9% saline in patients with end-stage renal disease undergoing cadaveric renal transplantation: a prospective randomized controlled trial. Anesth Analg 2015;120:123–129.
crossref pmid
13. Weinberg L, Harris L, Bellomo R, et al. Effects of intraoperative and early postoperative normal saline or Plasma-Lyte 148® on hyperkalaemia in deceased donor renal transplantation: a double-blind randomized trial. Br J Anaesth 2017;119:606–615.
crossref pmid
14. Fathi M, Massoudi N, Alirezaei A, Bakhtiyari M. Treatment of metabolic acidosis in altering inflammatory biomarkers in renal transplant recipients; a randomized clinical trial. Iran Red Crescent Med J 2018;20:e68102.
crossref
15. Arslantas R, Dogu Z, Cevik BE. Normal saline versus balanced crystalloid solutions for kidney transplantation. Transplant Proc 2019;51:2262–2264.
crossref pmid
16. Pourfakhr P, Shafiei M, Etezadi F, Khajavi MR, Moharari RS. Half saline-bicarbonate solution as intraoperative fluid replacement therapy leads to less acidosis and better early renal function during deceased-donor transplant. Exp Clin Transplant 2020;18:34–38.
crossref pmid
17. Prough DS, Bidani A. Hyperchloremic metabolic acidosis is a predictable consequence of intraoperative infusion of 0.9% saline. Anesthesiology 1999;90:1247–1249.
crossref pmid
18. Wilcox CS. Regulation of renal blood flow by plasma chloride. J Clin Invest 1983;71:726–735.
crossref pmid pmc
19. Ricaurte L, Vargas J, Lozano E, Díaz L; Organ Transplant Group. Anesthesia and kidney transplantation. Transplant Proc 2013;45:1386–1391.
crossref pmid
20. Etezadi F, Pourfakhr P, Mojtahedzade M, et al. Effects of tight versus non tight control of metabolic acidosis on early renal function after kidney transplantation. Daru 2012;20:36.
crossref pmid pmc
21. Bullivant EM, Wilcox CS, Welch WJ. Intrarenal vasoconstriction during hyperchloremia: role of thromboxane. Am J Physiol 1989;256(1 Pt 2):F152–F157.
crossref pmid
22. Hansen PB, Friis UG, Uhrenholt TR, Briggs J, Schnermann J. Intracellular signalling pathways in the vasoconstrictor response of mouse afferent arterioles to adenosine. Acta Physiol (Oxf) 2007;191:89–97.
crossref pmid
23. Willms CD, Dawidson IJ, Dickerman R, Drake D, Sandor ZF, Trevino G. Intraoperative blood volume expansion induces primary function after renal transplantation: a study of 96 paired cadaver kidneys. Transplant Proc 1991;23(1 Pt 2):1338–1339.
pmid
24. Dawidson IJ, Ar’Rajab A. Perioperative fluid and drug therapy during cadaver kidney transplantation. Clin Transpl 1992;267–284.
pmid
25. Trujillo-Zea JA, Aristizábal-Henao N, Fonseca-Ruiz N. Lactated Ringer’s vs. normal saline solution for renal transplantation: systematic review and meta-analysis. Rev Colomb de Anestesiol 2015;43:194–203.
crossref
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ORCID iDs

Abdullah Jahangir
https://orcid.org/0000-0002-7758-3318

Syeda Sahra
https://orcid.org/0000-0003-0119-3329

Muhammad Rafay Khan Niazi
https://orcid.org/0000-0002-4615-3147

Fasih Sami Siddiqui
https://orcid.org/0000-0002-5676-9172

Muhammad Yasir Anwar
https://orcid.org/0000-0001-9471-735X

Ahmad Jahangir
https://orcid.org/0000-0002-7758-3318

Elie J. El-Charabaty
https://orcid.org/0000-0003-4989-6023

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