Meta-analysis of high- versus low-chloride content in perioperative and critical care fluid resuscitation

M L Krajewski, K Raghunathan, S M Paluszkiewicz, C R Schermer, A D Shaw, M L Krajewski, K Raghunathan, S M Paluszkiewicz, C R Schermer, A D Shaw

Abstract

Background: The objective of this systematic review and meta-analysis was to assess the relationship between the chloride content of intravenous resuscitation fluids and patient outcomes in the perioperative or intensive care setting.

Methods: Systematic searches were performed of PubMed/MEDLINE, Embase and Cochrane Library (CENTRAL) databases in accordance with PRISMA guidelines. Randomized clinical trials, controlled clinical trials and observational studies were included if they compared outcomes in acutely ill or surgical patients receiving either high-chloride (ion concentration greater than 111 mmol/l up to and including 154 mmol/l) or lower-chloride (concentration 111 mmol/l or less) crystalloids for resuscitation. Endpoints examined were mortality, measures of kidney function, serum chloride, hyperchloraemia/metabolic acidosis, blood transfusion volume, mechanical ventilation time, and length of hospital and intensive care unit stay. Risk ratios (RRs), mean differences (MDs) or standardized mean differences (SMDs) and confidence intervals were calculated using fixed-effect modelling.

Results: The search identified 21 studies involving 6253 patients. High-chloride fluids did not affect mortality but were associated with a significantly higher risk of acute kidney injury (RR 1.64, 95 per cent c.i. 1.27 to 2.13; P < 0.001) and hyperchloraemia/metabolic acidosis (RR 2.87, 1.95 to 4.21; P < 0.001). High-chloride fluids were also associated with greater serum chloride (MD 3.70 (95 per cent c.i. 3.36 to 4.04) mmol/l; P < 0.001), blood transfusion volume (SMD 0.35, 0.07 to 0.63; P = 0.014) and mechanical ventilation time (SMD 0.15, 0.08 to 0.23; P < 0.001). Sensitivity analyses excluding heavily weighted studies resulted in non-statistically significant effects for acute kidney injury and mechanical ventilation time.

Conclusion: A weak but significant association between higher chloride content fluids and unfavourable outcomes was found, but mortality was unaffected by chloride content.

© 2014 The Authors. BJS published by John Wiley & Sons Ltd on behalf of BJS Society Ltd.

Figures

Fig 1
Fig 1
PRISMA flow diagram showing study selection. RCT, randomized controlled trial; CCT, controlled clinical trial
Fig 2
Fig 2
Forest plot illustrating mortality risk following volume resuscitation with high-chloride versus low-chloride intravenous fluids. Where necessary, mortality incidence was derived from reported survival. A Mantel–Haenszel fixed-effect model was used for meta-analysis. Risk ratios are shown with 95 per cent c.i. RCT, randomized controlled trial; CCT, controlled clinical trial
Fig 3
Fig 3
Forest plot illustrating acute kidney injury (AKI)/renal failure risk following volume resuscitation with high-chloride versus low-chloride intravenous fluids. A Mantel–Haenszel fixed-effect model was used for meta-analysis. Risk ratios are shown with 95 per cent c.i. RCT, randomized controlled trial; CCT, controlled clinical trial
Fig 4
Fig 4
Forest plot illustrating hyperchloraemia/metabolic acidosis risk following volume resuscitation with high-chloride versus low-chloride intravenous fluids. A Mantel–Haenszel fixed-effect model was used for meta-analysis. Risk ratios are shown with 95 per cent c.i. RCT, randomized controlled trial; CCT, controlled clinical trial
Fig 5
Fig 5
Forest plot illustrating mean(s.d.) blood transfusion volume following volume resuscitation with high-chloride versus low-chloride intravenous fluids. All included studies reporting this endpoint were randomized controlled trials. An inverse-variance fixed-effect model was used for meta-analysis. Standardized mean differences (SMDs) are shown with 95 per cent c.i.

References

    1. Myburgh JA, Mythen MG. Resuscitation fluids. N Engl J Med. 2013;369:1243–1251.
    1. Finfer S, Liu B, Taylor C, Bellomo R, Billot L, Cook D, et al. SAFE TRIPS Investigators. Resuscitation fluid use in critically ill adults: an international cross-sectional study in 391 intensive care units. Crit Care. 2010;14:R185.
    1. Veech RL. The toxic impact of parenteral solutions on the metabolism of cells: a hypothesis for physiological parenteral therapy. Am J Clin Nutr. 1986;44:519–551.
    1. Ho AM, Karmakar MK, Contardi LH, Ng SS, Hewson JR. Excessive use of normal saline in managing traumatized patients in shock: a preventable contributor to acidosis. J Trauma. 2001;51:173–177.
    1. Awad S, Allison SP, Lobo DN. The history of 0·9% saline. Clin Nutr. 2008;27:179–188.
    1. Guidet B, Soni N, Della Rocca G, Kozek S, Vallet B, Annane D, et al. A balanced view of balanced solutions. Crit Care. 2010;14:325.
    1. Lobo DN, Awad S. Should chloride-rich crystalloids remain the mainstay of fluid resuscitation to prevent ‘pre-renal’ acute kidney injury?: con. Kidney Int. 2014 [Epub ahead of print]
    1. Finfer S, Bellomo R, Boyce N, French J, Myburgh J, Norton R, et al. SAFE Study Investigators. A comparison of albumin and saline for fluid resuscitation in the intensive care unit. N Engl J Med. 2004;350:2247–2256.
    1. Myburgh JA, Finfer S, Bellomo R, Billot L, Cass A, Gattas D, et al. CHEST Investigators; Australian and New Zealand Intensive Care Society Clinical Trials Group. Hydroxyethyl starch or saline for fluid resuscitation in intensive care. N Engl J Med. 2012;367:1901–1911.
    1. Scheingraber S, Rehm M, Sehmisch C, Finsterer U. Rapid saline infusion produces hyperchloremic acidosis in patients undergoing gynecologic surgery. Anesthesiology. 1999;90:1265–1270.
    1. McFarlane C, Lee A. A comparison of Plasmalyte 148 and 0·9% saline for intra-operative fluid replacement. Anaesthesia. 1994;49:779–781.
    1. 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.
    1. Morgan TJ, Venkatesh B, Hall J. Crystalloid strong ion difference determines metabolic acid–base change during in vitro hemodilution. Crit Care Med. 2002;30:157–160.
    1. Waters JH, Gottlieb A, Schoenwald P, Popovich MJ, Sprung J, Nelson DR. Normal saline versus lactated Ringer's solution for intraoperative fluid management in patients undergoing abdominal aortic aneurysm repair: an outcome study. Anesth Analg. 2001;93:817–822.
    1. Handy JM, Soni N. Physiological effects of hyperchloraemia and acidosis. Br J Anaesth. 2008;101:141–150.
    1. Powell-Tuck J, Gosling P, Lobo DN, Allison SP, Carlson GL, Gore M, et al. British Consensus Guidelines on Intravenous Fluid Therapy for Adult Surgical Patients (GIFTASUP) 2013. 2011. [accessed 20 October ]
    1. Chowdhury AH, Cox EF, Francis ST, Lobo DN. A randomized, controlled, double-blind crossover study on the effects of 2-L infusions of 0·9% saline and Plasma-lyte® 148 on renal blood flow velocity and renal cortical tissue perfusion in healthy volunteers. Ann Surg. 2012;256:18–24.
    1. Hansen PB, Jensen BL, Skott O. Chloride regulates afferent arteriolar contraction in response to depolarization. Hypertension. 1998;32:1066–1070.
    1. Bullivant EM, Wilcox CS, Welch WJ. Intrarenal vasoconstriction during hyperchloremia: role of thromboxane. Am J Physiol. 1989;256:F152–F157.
    1. Imig JD, Passmore JC, Anderson GL, Jimenez AE. Chloride alters renal blood flow autoregulation in deoxycorticosterone-treated rats. J Lab Clin Med. 1993;121:608–613.
    1. Wilcox CS. Regulation of renal blood flow by plasma chloride. J Clin Invest. 1983;71:726–735.
    1. Kellum JA, Song M, Venkataraman R. Effects of hyperchloremic acidosis on arterial pressure and circulating inflammatory molecules in experimental sepsis. Chest. 2004;125:243–248.
    1. Kellum JA, Song M, Almasri E. Hyperchloremic acidosis increases circulating inflammatory molecules in experimental sepsis. Chest. 2006;130:962–967.
    1. Kellum JA, Song M, Li J. Science review: extracellular acidosis and the immune response: clinical and physiologic implications. Crit Care. 2004;8:331–336.
    1. McCluskey SA, Karkouti K, Wijeysundera D, Minkovich L, Tait G, Beattie WS. Hyperchloremia after noncardiac surgery is independently associated with increased morbidity and mortality: a propensity-matched cohort study. Anesth Analg. 2013;117:412–421.
    1. Yunos NM, Bellomo R, Hegarty C, Story D, Ho L, Bailey M. Association between a chloride-liberal vs chloride-restrictive intravenous fluid administration strategy and kidney injury in critically ill adults. JAMA. 2012;308:1566–1572.
    1. Shaw AD, Bagshaw SM, Goldstein SL, Scherer LA, Duan M, Schermer CR, et al. Major complications, mortality, and resource utilization after open abdominal surgery: 0·9% saline compared to Plasma-Lyte. Ann Surg. 2012;255:821–829.
    1. Burdett E, Dushianthan A, Bennett-Guerrero E, Cro S, Gan TJ, Grocott MP, et al. Perioperative buffered versus non-buffered fluid administration for surgery in adults. Cochrane Database Syst Rev. 2012;12:CD004089.
    1. Orbegozo Cortes D, Rayo Bonor A, Vincent JL. Isotonic crystalloid solutions: a structured review of the literature. Br J Anaesth. 2014;112:968–981.
    1. Moher D, Liberati A, Tetzlaff J, Altman DG. PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Ann Intern Med. 2009;151:264–269. W264.
    1. Higgins JPT, Green S. Cochrane Handbook for Systematic Reviews of Interventions Version 5.1.0. Oxford: The Cochrane Collaboration; 2011. [updated March ]., 2011.
    1. Wells GA, Shea B, O'Connell D, Peterson J, Welch V, Losos M, et al. The Newcastle–Ottawa Scale (NOS) for Assessing the Quality of Nonrandomised Studies in Meta Analyses. 2012. [accessed 10 July 2013]
    1. Hutton B, Joseph L, Fergusson D, Mazer CD, Shapiro S, Tinmouth A. Risks of harms using antifibrinolytics in cardiac surgery: systematic review and network meta-analysis of randomised and observational studies. BMJ. 2012;345:e5798.
    1. Dias S, Sutton AJ, Ades AE, Welton NJ. Evidence synthesis for decision making 2: a generalized linear modeling framework for pairwise and network meta-analysis of randomized controlled trials. Med Decis Making. 2013;33:607–617.
    1. Hozo SP, Djulbegovic B, Hozo I. Estimating the mean and variance from the median, range, and the size of a sample. BMC Med Res Methodol. 2005;5:13.
    1. Higgins JP, White IR, Anzures-Cabrera J. Meta-analysis of skewed data: combining results reported on log-transformed or raw scales. Stat Med. 2008;27:6072–6092.
    1. Zar JH. Biostatistical Analysis. Upper Saddle River: Prentice Hall; 1999. 4th edn.
    1. Higgins JP, Thompson SG, Deeks JJ, Altman DG. Measuring inconsistency in meta-analyses. BMJ. 2003;327:557–560.
    1. Bailar JC, Hoaglin DC. Medical Uses of Statistics. Hoboken: John Wiley & Sons; 2009. 3rd edn.
    1. Hasman H, Cinar O, Uzun A, Cevik E, Jay L, Comert B. A randomized clinical trial comparing the effect of rapidly infused crystalloids on acid–base status in dehydrated patients in the emergency department. Int J Med Sci. 2012;9:59–64.
    1. Berger MM, Pictet A, Revelly JP, Frascarolo P, Chioléro RL. Impact of a bicarbonated saline solution on early resuscitation after major burns. Intensive Care Med. 2000;26:1382–1385.
    1. Cho YS, Lim H, Kim SH. Comparison of lactated Ringer's solution and 0·9% saline in the treatment of rhabdomyolysis induced by doxylamine intoxication. Emerg Med J. 2007;24:276–280.
    1. Chua HR, Venkatesh B, Stachowski E, Schneider AG, Perkins K, Ladanyi S, et al. Plasma-Lyte 148 vs 0·9% saline for fluid resuscitation in diabetic ketoacidosis. J Crit Care. 2012;27:138–145.
    1. Cieza JA, Hinostroza J, Huapaya JA, Leon CP. Sodium chloride 0·9% versus lactated Ringer in the management of severely dehydrated patients with choleriform diarrhoea. J Infect Dev Ctries. 2013;7:528–532.
    1. Khajavi MR, Etezadi F, Moharari RS, Imani F, Meysamie AP, Khashayar P, et al. Effects of normal saline vs. lactated ringer's during renal transplantation. Ren Fail. 2008;30:535–539.
    1. 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.
    1. Mahajan V, Sajan SS, Sharma A, Kaur J. Ringers lactate vs normal saline for children with acute diarrhea and severe dehydration – a double blind randomized controlled trial. Indian Pediatr. 2012;49:963–968.
    1. Mahler SA, Conrad SA, Wang H, Arnold TC. Resuscitation with balanced electrolyte solution prevents hyperchloremic metabolic acidosis in patients with diabetic ketoacidosis. Am J Emerg Med. 2011;29:670–674.
    1. 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.
    1. O'Malley CM, Frumento RJ, Hardy MA, Benvenisty AI, Brentjens TE, Mercer JS, 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.
    1. Takil A, Eti Z, Irmak P, Yilmaz GöğüşF. Early postoperative respiratory acidosis after large intravascular volume infusion of lactated Ringer's solution during major spine surgery. Anesth Analg. 2002;95:294–298.
    1. Van Zyl DG, Rheeder P, Delport E. Fluid management in diabetic-acidosis – Ringer's lactate versus normal saline: a randomized controlled trial. QJM. 2012;105:337–343.
    1. Wu BU, Hwang JQ, Gardner TH, Repas K, Delee R, Yu S, et al. Lactated Ringer's solution reduces systemic inflammation compared with saline in patients with acute pancreatitis. Clin Gastroenterol Hepatol. 2011;9:710–717. e711.
    1. Young JB, Utter GH, Schermer CR, Galante JM, Phan HH, Yang Y, et al. Saline versus Plasma-Lyte A in initial resuscitation of trauma patients: a randomized trial. Ann Surg. 2014;259:255–262.
    1. Yunos NM, Kim IB, Bellomo R, Bailey M, Ho L, Story D, et al. The biochemical effects of restricting chloride-rich fluids in intensive care. Crit Care Med. 2011;39:2419–2424.
    1. Zunini GS, Rando KA, Cox RG. Fluid replacement in craniofacial pediatric surgery: normal saline or Ringer's lactate? J Craniofac Surg. 2011;22:1370–1374.
    1. Williams EL, Hildebrand KL, McCormick SA, Bedel MJ. The effect of intravenous lactated Ringer's solution versus 0·9% sodium chloride solution on serum osmolality in human volunteers. Anesth Analg. 1999;88:999–1003.
    1. Reid F, Lobo DN, Williams RN, Rowlands BJ, Allison SP. (Ab)normal saline and physiological Hartmann's solution: a randomized double-blind crossover study. Clin Sci (Lond) 2003;104:17–24.
    1. Raghunathan K, Shaw A, Nathanson B, Sturmer T, Brookhart A, Stefan MS, et al. Association between the choice of IV crystalloid and in-hospital mortality among critically ill adults with sepsis. Crit Care Med. 2014;42:1585–1591.
    1. Cohen J. A power primer. Psychol Bull. 1992;112:155–159.
    1. Hofmann A, Ozawa S, Farrugia A, Farmer SL, Shander A. Economic considerations on transfusion medicine and patient blood management. Best Pract Res Clin Anaesthesiol. 2013;27:59–68.
    1. Marik PE, Corwin HL. Efficacy of red blood cell transfusion in the critically ill: a systematic review of the literature. Crit Care Med. 2008;36:2667–2674.
    1. Todd SR, Malinoski D, Muller PJ, Schreiber MA. Lactated Ringer's is superior to normal saline in the resuscitation of uncontrolled hemorrhagic shock. J Trauma. 2007;62:636–639.
    1. Ahn HJ, Yang M, Gwak MS, Koo MS, Bang SR, Kim GS, et al. Coagulation and biochemical effects of balanced salt-based high molecular weight vs saline-based low molecular weight hydroxyethyl starch solutions during the anhepatic period of liver transplantation. Anaesthesia. 2008;63:235–242.
    1. Bradburn MJ, Deeks JJ, Berlin JA, Russell LocalioA. Much ado about nothing: a comparison of the performance of meta-analytical methods with rare events. Stat Med. 2007;26:53–77.
    1. Sweeting MJ, Sutton AJ, Lambert PC. What to add to nothing? Use and avoidance of continuity corrections in meta-analysis of sparse data. Stat Med. 2004;23:1351–1375.
    1. Sutton AJ, Cooper NJ, Lambert PC, Jones DR, Abrams KR, Sweeting MJ. Meta-analysis of rare and adverse event data. Expert Rev Pharmacoecon Outcomes Res. 2002;2:367–379.
    1. Golder S, Loke YK, Bland M. Meta-analyses of adverse effects data derived from randomised controlled trials as compared to observational studies: methodological overview. PLoS Med. 2011;8:e1001026.
    1. Guyatt GH, Oxman AD, Santesso N, Helfand M, Vist G, Kunz R, et al. GRADE guidelines: 12. Preparing summary of findings tables-binary outcomes. J Clin Epidemiol. 2013;66:158–172.
    1. Soreide K, Alderson D, Bergenfelz A, Beynon J, Connor S, Deckelbaum DL, et al. International Research Collaboration in Surgery (IRIS) ad-hoc working group. Strategies to improve clinical research in surgery through international collaboration. Lancet. 2013;382:1140–1151.
    1. Australian New Zealand Clinical Trials Registry (ANZCTR) 0·9% Saline vs. Plasma-Lyte 148 for Intensive Care Fluid Therapy (The SPLIT Study) 2013. [accessed 22 May 2014]

Source: PubMed

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