Association Between Elevated RBC Distribution Width and Multiple Organ Dysfunction in Pediatric Critical Illness.


Journal

Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies
ISSN: 1529-7535
Titre abrégé: Pediatr Crit Care Med
Pays: United States
ID NLM: 100954653

Informations de publication

Date de publication:
09 2020
Historique:
pubmed: 24 7 2020
medline: 7 1 2021
entrez: 24 7 2020
Statut: ppublish

Résumé

RBC distribution width, a part of the complete blood count, has been shown in several published studies to be a strong biomarker of adverse outcomes. We sought to determine the association between admission RBC distribution width value and clinical outcomes including multiple organ dysfunction, mechanical ventilation days, PICU length of stay, and hospital length of stay in children admitted to the PICU. Single center, retrospective study. A tertiary pediatric hospital in the United States. All subjects admitted to the PICU from 2016 to 2017. Greater than 21 years old, pregnancy, and history of packed RBC transfusion within 120 days prior to admission. None. One-thousand five-hundred one subjects were screened and 856 were included in data analysis. RBC distribution width value was categorized into four separate groups: group I (RBC distribution width < 13.4%), group II (13.4-14.3%), group III (14.4-15.7%), and group IV (RBC distribution width > 15.7%). Increased RBC distribution width at admission was associated with multiple organ dysfunction syndrome in the first 7 days (group I = 11.8% vs group IV = 30.1%; p < 0.0001) (odds ratio, 3.22; 95% CI, 1.95-5.30; p < 0.0001). Increased RBC distribution width was associated with increased median mechanical ventilation duration (group IV = 7 d vs group I = 5 d; p = 0.001), median hospital length of stay (group IV = 13 d vs group I = 5 d; p < 0.0001), and median PICU length of stay (group IV = 4 d vs group I = 3 d; p = 0.01). Mortality was not statistically associated with admission RBC distribution width (p = 0.12). PICU admission RBC distribution width values greater than 15.7% obtained upon admission to the PICU in patients who have not received a RBC transfusion are associated with multiple organ dysfunction syndrome in the first 7 days of admission, increased duration of mechanical ventilation, and increased hospital length of stay.

Identifiants

pubmed: 32701753
doi: 10.1097/PCC.0000000000002487
pii: 00130478-202009000-00041
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e740-e746

Subventions

Organisme : NCRR NIH HHS
ID : UL1 RR029884
Pays : United States
Organisme : NIGMS NIH HHS
ID : K23 GM110496
Pays : United States

Références

Qurtom HA, al-Saleh QA, Lubani MM, et al. The value of red cell distribution width in the diagnosis of anaemia in children. Eur J Pediatr 1989; 148:745–748
Scharte M, Fink MP. Red blood cell physiology in critical illness. Crit Care Med 2003; 31:S651–S657
Bazick HS, Chang D, Mahadevappa K, et al. Red cell distribution width and all-cause mortality in critically ill patients. Crit Care Med 2011; 39:1913–1921
Lee H, Kong SY, Sohn JY, et al. Elevated red blood cell distribution width as a simple prognostic factor in patients with symptomatic multiple myeloma. Biomed Res Int 2014; 2014:145619
Grant BJ, Kudalkar DP, Muti P, et al. Relation between lung function and RBC distribution width in a population-based study. Chest 2003; 124:494–500
Wen Y. High red blood cell distribution width is closely associated with risk of carotid artery atherosclerosis in patients with hypertension. Exp Clin Cardiol 2010; 15:37–40
Wang F, Pan W, Pan S, et al. Red cell distribution width as a novel predictor of mortality in ICU patients. Ann Med 2011; 43:40–46
Ramby AL, Goodman DM, Wald EL, et al. Red blood cell distribution width as a pragmatic marker for outcome in pediatric critical illness. PLoS One 2015; 10:e0129258
Said AS, Spinella PC, Hartman ME, et al. RBC distribution width: Biomarker for red cell dysfunction and critical illness outcome? Pediatr Crit Care Med 2017; 18:134–142
Wetzel RC, Sachedeva R, Rice TB. Are all ICUs the same? Paediatr Anaesth 2011; 21:787–793
Slater A, Shann F, Pearson G. Paediatric Index of Mortality (PIM) study group. Intensive Care Med 2003; 29:278–285
Chu Y, Yuan Z, Meng M, et al. Red blood cell distribution width as a risk factor for inhospital mortality in obstetric patients admitted to an intensive care unit: A single centre retrospective cohort study. BMJ Open 2017; 7:e012849
Ku NS, Kim HW, Oh HJ, et al. Red blood cell distribution width is an independent predictor of mortality in patients with gram-negative bacteremia. Shock 2012; 38:123–127
World Health Organization: Anaemia as a public health problem. In: Nutritional Anaemias: Tools for Effective Prevention and Control. 2017, pp Geneva, Switzerland, World Health Organization, 7
Harris PA, Taylor R, Thielke R, et al. Research electronic data capture (REDCap)–a metadata-driven methodology and workflow process for providing translational research informatics support. J Biomed Inform 2009; 42:377–381
Goldstein B, Giroir B, Randolph A; International Consensus Conference on Pediatric Sepsis: International pediatric sepsis consensus conference: Definitions for sepsis and organ dysfunction in pediatrics. Pediatr Crit Care Med 2005; 6:2–8
Constantino BT. The red cell histogram and the dimorphic red cell population. Lab Med 2011; 42:300–308
Meynaar IA, Knook AH, Coolen S, et al. Red cell distribution width as predictor for mortality in critically ill patients. Neth J Med 2013; 71:488–493
Ju XF, Wang F, Wang L, et al. Dynamic change of red cell distribution width levels in prediction of hospital mortality in Chinese elderly patients with septic shock. Chin Med J (Engl) 2017; 130:1189–1195
Purtle SW, Moromizato T, McKane CK, et al. The association of red cell distribution width at hospital discharge and out-of-hospital mortality following critical illness*. Crit Care Med 2014; 42:918–929
Sadaka F, O’Brien J, Prakash S. Red cell distribution width and outcome in patients with septic shock. J Intensive Care Med 2013; 28:307–313
Typpo KV, Lacroix JR. Monitoring severity of multiple organ dysfunction syndrome: New and progressive multiple organ dysfunction syndrome, scoring systems. Pediatr Crit Care Med 2017; 18:S17–S23

Auteurs

Sonia Matehuala (S)

Section of Critical Care, Department of Pediatrics, Arkansas Children's Hospital, Little Rock, AR.

Sanjiv Pasala (S)

Section of Critical Care, Department of Pediatrics, Arkansas Children's Hospital, Little Rock, AR.

Anthony Goudie (A)

Arkansas Center for Health Improvement, Little Rock, AR.

Richard Fiser (R)

Section of Critical Care, Department of Pediatrics, Arkansas Children's Hospital, Little Rock, AR.

Scott Weiss (S)

Section of Critical Care, Department of Pediatrics, Arkansas Children's Hospital, Little Rock, AR.
Arkansas Center for Health Improvement, Little Rock, AR.
Department of Anesthesiology and Critical Care, Children's Hospital of Philadelphia, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.
Pediatric Sepsis Program, Children's Hospital of Philadelphia, Philadelphia, PA.
Department of Anesthesiology and Critical Care Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.
Section of Hematology/Oncology, Department of Pediatrics, Arkansas Children's Hospital, Little Rock, AR.
Stanford University, Palo Alto, CA.

Katherine Irby (K)

Section of Critical Care, Department of Pediatrics, Arkansas Children's Hospital, Little Rock, AR.

Shelley Crary (S)

Section of Hematology/Oncology, Department of Pediatrics, Arkansas Children's Hospital, Little Rock, AR.

Angela Wang (A)

Stanford University, Palo Alto, CA.

Ronald Sanders (R)

Section of Critical Care, Department of Pediatrics, Arkansas Children's Hospital, Little Rock, AR.

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