Red cell distribution width/albumin ratio and 90-day mortality after burn surgery

Young Joo Seo , Jihion Yu , Jun-Young Park , Narea Lee , Jiwoong Lee , Ji Hyun Park , Hee Yeong Kim , Yu-Gyeong Kong , Young-Kug Kim

Burns & Trauma ›› 2022, Vol. 10 ›› Issue (1) : tkab050

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Burns & Trauma ›› 2022, Vol. 10 ›› Issue (1) :tkab050 DOI: 10.1093/burnst/tkab050
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Red cell distribution width/albumin ratio and 90-day mortality after burn surgery
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Abstract

Background: Red cell distribution width (RDW) and serum albumin concentration are associated with postoperative outcomes. However, the usefulness of the RDW/albumin ratio in burn surgery remains unclear. Therefore, we evaluated the association between RDW/albumin ratio and 90-day mortality after burn surgery. Methods: Between 2013 and 2020, a retrospective review of patients in a burn intensive care unit (ICU) was performed. Receiver operating characteristic curve, multivariate Cox logistic regression, multivariate logistic regression and Kaplan–Meier analyses were conducted to evaluate the associ-ation between RDW/albumin ratio and 90-day mortality after burn surgery. Additionally, prolonged ICU stay rate (>60 days) and ICU stay were assessed. Results: Ninety-day mortality was 22.5% (210/934) in burn patients. Risk factors for 90-day mortality were RDW/albumin ratio at postoperative day 1, age, American Society of Anesthesiologists physical status, diabetes mellitus, inhalation injury, total body surface area burned, hypotensive event and red blood cell transfusion volume. The area under the curve of the RDW/albumin ratio at postoperative day 1 to predict 90-day mortality, after adjusting for age and total body surface area burned, was 0.875 (cut-off value, 6.8). The 90-day mortality was significantly higher in patients with RDW/albumin ratio >6.8 than in those with RDW/albumin ratio ≤6.8 (49.2% vs 12.3%, p < 0.001). Prolonged ICU stay rate and ICU stay were significantly higher and longer in patients with RDW/albumin ratio >6.8 than in those with RDW/albumin ratio ≤6.8 (34.5% vs 26.5%; 21 [11– 38] vs 18 [7–32] days). Conclusion: RDW/albumin ratio >6.8 on postoperative day 1 was associated with higher 90-day mortality, higher prolonged ICU stay rate and longer ICU stay after burn surgery.

Keywords

Red cell distribution width / Albumin ratio / Mortality / Mortality / Burn / Risk factor / Surgery

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Young Joo Seo, Jihion Yu, Jun-Young Park, Narea Lee, Jiwoong Lee, Ji Hyun Park, Hee Yeong Kim, Yu-Gyeong Kong, Young-Kug Kim. Red cell distribution width/albumin ratio and 90-day mortality after burn surgery. Burns & Trauma, 2022, 10 (1) : tkab050 DOI:10.1093/burnst/tkab050

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References

[1]

Zhang P, Zou B, Liou YC, Huang C. The pathogenesis and diagnosis of sepsis post burn injury. Burns Trauma. 2021; 9: tkaa047. https://doi.org/10.1093/burnst/tkaa047.

[2]

Lee KC, Joory K, Moiemen NS. History of burns: the past, present and the future. Burns Trauma. 2014; 2(4): 169-80. https://doi.org/10.4103/2321-3868.143620.

[3]

Brusselaers N, Monstrey S, Vogelaers D, Hoste E, Blot S. Severe burn injury in Europe: a systematic review of the incidence, etiology, morbidity, and mortality. Crit Care. 2010; 14(5): R188. https://doi.org/10.1186/cc9300.

[4]

Salvagno GL, Sanchis-Gomar F, Picanza A, Lippi G. Red blood cell distribution width: a simple parameter with multiple clinical applications. Crit Rev Clin Lab Sci. 2015; 52(2): 86-105. https://doi.org/10.3109/10408363.2014.992064.

[5]

Kong T, Park JE, Park YS, Lee HS, You JS, Chung HS, et al. Usefulness of serial measurement of the red blood cell distribution width to predict 28-day mortality in patients with trauma. Am J Emerg Med. 2017; 35(12): 1819-27. https://doi.org/10.1016/j.ajem.2017.06.008.

[6]

Guo J, Qin Q, Hu H, Zhou D, Sun Y, Deng A. Red cell distribution width (RDW) as a prognostic tool in burn patients. Clin Lab. 2016; 62(10): 1973-8. https://doi.org/10.7754/Clin.Lab.2016.160222.

[7]

Don BR, Kaysen G. Serum albumin: relationship to inflammation and nutrition. Semin Dial. 2004; 17(6): 432-7. https://doi.org/10.1111/j.0894-0959.2004.17603.x.

[8]

Seo YJ, Kong YG, Yu J, Park JH, Kim SJ, Kim HY, et al. The prognostic nutritional index on postoperative day one is associated with one-year mortality after burn surgery in elderly patients. Burns Trauma. 2021; 9:tkaa043. https://doi.org/10.1093/burnst/tkaa043.

[9]

Kim HY, Kong YG, Park JH, Kim YK. Acute kidney injury after burn surgery: preoperative neutrophil/lymphocyte ratio as a predictive factor. Acta Anaesthesiol Scand. 2019; 63(2): 240-7. https://doi.org/10.1111/aas.13255.

[10]

Rae L, Fidler P, Gibran N. The physiologic basis of burn shock and the need for aggressive fluid resuscitation. Crit Care Clin. 2016; 32(4): 491-505. https://doi.org/10.1016/j.ccc.2016.06.001.

[11]

Lippi G, Targher G, Montagnana M, Salvagno GL, Zoppini G, Guidi GC. Relation between red blood cell distribution width and inflammatory biomarkers in a large cohort of uns elected outpatients. Arch Pathol Lab Med. 2009; 133(4): 628-32. https://doi.org/10.5858/133.4.628.

[12]

Hou H, Sun T, Li C, Li Y, Guo Z, Wang W, et al. An overall and dose-response meta-analysis of red blood cell distribution width and CVD outcomes. Sci Rep. 2017; 7: 43420. https://doi.org/10.1038/srep43420.

[13]

Eljaiek R, Heylbroeck C, Dubois MJ. Albumin administration for fluid resuscitation in burn patients: a systematic review and meta-analysis. Burns. 2017; 43(1): 17-24. https://doi.org/10.1016/j.burns.2016.08.001.

[14]

Labgaa I, Joliat GR, Kefleyesus A, Mantziari S, Schäfer M, Demartines N, et al. Is postoperative decrease of serum albumin an early predictor of complications after major abdominal surgery? A prospective cohort study in a European Centre. BMJ Open. 2017; 7(4): e013966. https://doi.org/10.1136/bmjopen-2016-013966.

[15]

Hübner M, Mantziari S, Demartines N, Pralong F, Coti-Bertrand P, Schäfer M. Postoperative albumin drop is a marker for surgical stress and a predictor for clinical outcome: a pilot study. Gastroenterol Res Pract. 2016; 2016: 8743187. https://doi.org/10.1155/2016/8743187.

[16]

Yoo JW, Ju S, Lee SJ, Cho YJ, Lee JD, Kim HC. Red cell distribution width/albumin ratio is associated with 60-day mortality in patients with acute respiratory distress syndrome. Infect Dis (Lond). 2020; 52(4): 266-70. https://doi.org/10.1080/23744235.2020.1717599.

[17]

Zhao N, Hu W, Wu Z, Wu X, Li W, Wang Y, et al. The red blood cell distribution width-albumin ratio: a promising predictor of mortality in stroke patients. Int J Gen Med. 2021; 14: 3737-47. https://doi.org/10.2147/ijgm.S322441.

[18]

Oh HJ, Park JT, Kim JK, Yoo DE, Kim SJ, Han SH, et al. Red blood cell distribution width is an independent predictor of mortality in acute kidney injury patients treated with continuous renal replacement therapy. Nephrol Dial Transplant. 2012; 27(2): 589-94. https://doi.org/10.1093/ndt/gfr307.

[19]

Bazick HS, Chang D, Mahadevappa K, Gibbons FK, Christopher KB. Red cell distribution width and all-cause mortality in critically ill patients. Crit Care Med. 2011; 39(8): 1913-21. https://doi.org/10.1097/CCM.0b013e31821b85c6.

[20]

Spadaro S, Taccone FS, Fogagnolo A, Franchi F, Scolletta S, Ragazzi R, et al. The effects of blood transfusion on red blood cell distribution width in critically ill patients: a pilot study. Transfusion. 2018; 58(8): 1863-9. https://doi.org/10.1111/trf.14759.

[21]

Felker GM, Allen LA, Pocock SJ, Shaw LK, McMurray JJ, Pfeffer MA, et al. Red cell distribution width as a novel prognostic marker in heart failure: data from the CHARM program and the Duke databank. J Am Coll Cardiol. 2007; 50(1): 40-7. https://doi.org/10.1016/j.jacc.2007.02.067.

[22]

Brown M, Nassoiy S, Plackett T, Luchette F, Posluszny J, Jr. Red blood cell distribution width and outcome in trauma patients. J Osteopath Med. 2021; 121(2): 221-8. https://doi.org/10.1515/jom-2020-0089.

[23]

Massin MM.Relation between red cell distribution width and clinical outcome after surgery for congenital heart disease in children. Pediatr Cardiol. 2012; 33(7): 1021-5. https://doi.org/10.1007/s00246-012-0220-0.

[24]

Yu J, Kim HY, Kong YG, Park JH, Seo YJ, Kim YK. De Ritis ratio as a predictor of 1-year mortality after burn surgery. Burns. 2021; 47(8): 1865-72. https://doi.org/10.1016/j.burns.2021.02.001.

[25]

Bittner EA, Shank E, Woodson L, Martyn JA. Acute and perioperative care of the burn-injured patient. Anesthesiology. 2015; 122(2): 448-64. https://doi.org/10.1097/aln.0000000000000559.

[26]

Yang B, Cai YQ, Wang XD. The impact of diabetes mellitus on mortality and infection outcomes in burn patients: a meta-analysis. Eur Rev Med Pharmacol Sci. 2021; 25(6): 2481-92. https://doi.org/10.26355/eurrev_202103_25411.

[27]

Palmieri TL, Caruso DM, Foster KN, Cairns BA, Peck MD, Gamelli RL, et al. Effect of blood transfusion on outcome after major burn injury: a multicenter study. Crit Care Med. 2006; 34(6): 1602-7. https://doi.org/10.1097/01.Ccm.0000217472.97524.0e.

[28]

Gregory A, Stapelfeldt WH, Khanna AK, Smischney NJ, Boero IJ, Chen Q, et al. Intraoperative hypotension is associated with adverse clinical outcomes after noncardiac surgery. Anesth Analg. 2021; 132(6): 1654-65. https://doi.org/10.1213/ANE.0000000000005325.

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