Identifying factors to minimize phlebotomy-induced blood loss in the pediatric intensive care unit
- PMID: 21499175
- DOI: 10.1097/PCC.0b013e318219681d
Identifying factors to minimize phlebotomy-induced blood loss in the pediatric intensive care unit
Abstract
Objective: Phlebotomy-induced blood loss in critically ill children is common, contributes to anemia, and may be avoidable. We aimed to identify factors associated with phlebotomy-induced blood loss.
Design: Prospective observational study, single-center tertiary children's hospital.
Setting: Pediatric intensive care unit.
Patients: A total of 63 patients admitted to the pediatric intensive care unit for >48 hrs from 2004 to 2005.
Interventions: None.
Measurements and main results: Phlebotomy resulted in a mean blood volume loss of 2.5 ± 1.4 mL per draw, 7.1 ± 5.3 mL per day, and 34 ± 37 mL per pediatric intensive care unit stay, of which 1.4 ± 1.1 mL per draw, 3.8 ± 3.6 mL per day, and 23 ± 31 mL per pediatric intensive care unit stay were discarded as excess. This excess represents 210% ± 174% of the volume requested by the laboratory and a 110% overdraw. Blood drawn from central venous catheters had significantly greater overdraw volumes, 254% ± 112%, compared to those of arterial, 168% ± 44%, and peripheral intravenous catheters, 143% ± 39%, p < .001. Blood draws sent for one test had an associated overdraw of 278% ± 81%, compared to draws sent for two, 168% ± 48%, three 173% ± 4%, and four or greater tests 55% ± 5%, p < .001. Patients <10 kg had significantly greater mean volumes of blood loss/kg/day compared to patients ≥ 10 kg, p < .001.
Conclusion: Blood drawn in excess of phlebotomy requirements exceeds the blood volume loss drawn for phlebotomy by two fold. Using indwelling catheters for phlebotomy often requires a discard volume to be drawn before obtaining the laboratory sample. Consolidating phlebotomy tests and using a closed system may decrease the amount of blood overdrawn and minimize overall phlebotomy-induced blood loss.
Similar articles
-
Phlebotomy overdraw in the neonatal intensive care nursery.Pediatrics. 2000 Aug;106(2):E19. doi: 10.1542/peds.106.2.e19. Pediatrics. 2000. PMID: 10920175
-
[Blood volume for biochemistry determinations--laboratory needs and everyday practice].Przegl Lek. 2014;71(1):10-3. Przegl Lek. 2014. PMID: 24712262 Polish.
-
Blood conservation in the intensive care unit.Crit Care Med. 2003 Dec;31(12 Suppl):S715-20. doi: 10.1097/01.CCM.0000099350.50651.46. Crit Care Med. 2003. PMID: 14724470 Review.
-
Investigation into the effect of closed-system suctioning on the frequency of pediatric ventilator-associated pneumonia in a developing country.Pediatr Crit Care Med. 2012 Jan;13(1):e25-32. doi: 10.1097/PCC.0b013e31820ac0a2. Pediatr Crit Care Med. 2012. PMID: 21283045 Clinical Trial.
-
Transfusion practice in the critically ill.Crit Care Med. 2003 Dec;31(12 Suppl):S668-71. doi: 10.1097/01.CCM.0000099348.99451.84. Crit Care Med. 2003. PMID: 14724464 Review.
Cited by
-
A Standard Push-Pull Protocol for Waste-Free Sampling in the Pediatric Intensive Care Unit.J Infus Nurs. 2018 May/Jun;41(3):189-197. doi: 10.1097/NAN.0000000000000279. J Infus Nurs. 2018. PMID: 29659467 Free PMC article.
-
Intestinal fatty acid-binding protein as a diagnostic marker for complicated and uncomplicated necrotizing enterocolitis: a prospective cohort study.PLoS One. 2015 Mar 20;10(3):e0121336. doi: 10.1371/journal.pone.0121336. eCollection 2015. PLoS One. 2015. PMID: 25793701 Free PMC article.
-
Every Tube Counts: reducing extra tubes drawn in the emergency department.BMJ Open Qual. 2023 Nov;12(4):e002447. doi: 10.1136/bmjoq-2023-002447. BMJ Open Qual. 2023. PMID: 37931984 Free PMC article.
-
2016 proceedings of the National Heart, Lung, and Blood Institute's scientific priorities in pediatric transfusion medicine.Transfusion. 2017 Jun;57(6):1568-1581. doi: 10.1111/trf.14100. Epub 2017 Mar 28. Transfusion. 2017. PMID: 28369923 Free PMC article. No abstract available.
-
Engineering of a miniaturized, robotic clinical laboratory.Bioeng Transl Med. 2018 Jan 19;3(1):58-70. doi: 10.1002/btm2.10084. eCollection 2018 Jan. Bioeng Transl Med. 2018. PMID: 29376134 Free PMC article.
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Medical