TY - JOUR
T1 - Peri-operative red blood cell transfusion in neonates and infants
T2 - NEonate and Children audiT of Anaesthesia pRactice IN Europe: A prospective European multicentre observational study
AU - Fuchs, Alexander
AU - Disma, Nicola
AU - Virág, Katalin
AU - Ulmer, Francis
AU - Habre, Walid
AU - de Graaff, Jurgen C.
AU - Riva, Thomas
AU - Breschan, Christian
AU - Likar, Rudolf
AU - Platzer, Manuela
AU - Edelman, Isole
AU - Eger, Johanes
AU - Heschl, Stefan
AU - Messerer, Brigitte
AU - Vittinghof, Maria
AU - Kroess, Ruth
AU - Stichlberger, Martina
AU - Kahn, David
AU - Pirotte, Thierry
AU - Pregardien, Caroline
AU - Veyckemans, Francis
AU - Stevens, France
AU - Berghmans, Johan
AU - Bauters, Annemie
AU - De Baerdemaeker, Luc
AU - De Hert, Stefan
AU - Lapage, Koen
AU - Parashchanka, Aliaksandra
AU - Van Limmen, Jurgen
AU - Wyffels, Piet
AU - Lauweryns, Julie
AU - Najafi, Nadia
AU - Vundelinckx, Joris
AU - Butković, Diana
AU - Sorić, Ivana Kerovec
AU - Kralik, Sandra
AU - Markić, Ana
AU - Azman, Josip
AU - Markic, Josko
AU - Pupacic, Daniela
AU - Frelich, Michal
AU - Reimer, Petr
AU - Urbanec, René
AU - Cajková, Petra
AU - Mixa, Vladimír
AU - Sedláčková, Yvona
AU - Buhre, Wolfgang
AU - Hendriks, Mark
AU - Pieters, Barbe
AU - Van Zaane, Bas
N1 - Funding Information:
Detailed study design and data collection for the NECTARINE cohort have been described previously.17,18 In brief, NECTARINE is a European multicentre, prospective, observational cohort study funded by the European Society of Anaesthesiology and Intensive Care (ESAIC) through the Clinical Trial Network grant. Peri-operative anaesthesia management data on children aged from birth to 60 weeks PMA was collected in 165 European centres. The ESAIC selected participating centres through a ‘call for centre’. Each country was represented by a national co-ordinator, and all participating centres obtained ethical approval in accordance with local or national requirements (approval forms available online: https://www.esaic.org/research/clinical-trial-network/ completed-trials/nectarine/). Following ethics approval of all participating centres, patients were recruited over a 3-month period at each centre, with overall recruitment between 1 March 2016 and 31 January 2017. The study was registered (ClinicalTrials.gov, NCT02350348). This manuscript adheres to the applicable Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) guidelines (www.strobe-statement.org).
Funding Information:
European Society of Anaesthesiology and Intensive Care Medicine (ESAIC) and Clinical Trial Network (CTN). The Association of Paediatric Anaesthetists of Great Britain and Ireland (APAGBI) funded the study for the follow-up of patients enrolled in the UK.
Publisher Copyright:
Copyright © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the European Society of Anaesthesiology and Intensive Care.
PY - 2022/3/1
Y1 - 2022/3/1
N2 - BACKGROUND Little is known about current clinical practice concerning peri-operative red blood cell transfusion in neonates and small infants. Guidelines suggest transfusions based on haemoglobin thresholds ranging from 8.5 to 12 g dl-1, distinguishing between children from birth to day 7 (week 1), from day 8 to day 14 (week 2) or from day 15 (≥week 3) onwards. OBJECTIVE To observe peri-operative red blood cell transfusion practice according to guidelines in relation to patient outcome. DESIGN A multicentre observational study. SETTING The NEonate-Children sTudy of Anaesthesia pRactice IN Europe (NECTARINE) trial recruited patients up to 60 weeks' postmenstrual age undergoing anaesthesia for surgical or diagnostic procedures from 165 centres in 31 European countries between March 2016 and January 2017. PATIENTS The data included 5609 patients undergoing 6542 procedures. Inclusion criteria was a peri-operative red blood cell transfusion. MAIN OUTCOME MEASURES The primary endpoint was the haemoglobin level triggering a transfusion for neonates in week 1, week 2 and week 3. Secondary endpoints were transfusion volumes, 'delta haemoglobin' (preprocedure - transfusion-triggering) and 30-day and 90-day morbidity and mortality. RESULTS Peri-operative red blood cell transfusions were recorded during 447 procedures (6.9%). The median haemoglobin levels triggering a transfusion were 9.6 [IQR 8.7 to 10.9] g dl-1 for neonates in week 1, 9.6 [7.7 to 10.4] g dl-1 in week 2 and 8.0 [7.3 to 9.0] g dl-1 in week 3. The median transfusion volume was 17.1 [11.1 to 26.4] ml kg-1 with a median delta haemoglobin of 1.8 [0.0 to 3.6] g dl-1. Thirty-day morbidity was 47.8% with an overall mortality of 11.3%. CONCLUSIONS Results indicate lower transfusion-triggering haemoglobin thresholds in clinical practice than suggested by current guidelines. The high morbidity and mortality of this NECTARINE sub-cohort calls for investigative action and evidence-based guidelines addressing perioperative red blood cell transfusions strategies.
AB - BACKGROUND Little is known about current clinical practice concerning peri-operative red blood cell transfusion in neonates and small infants. Guidelines suggest transfusions based on haemoglobin thresholds ranging from 8.5 to 12 g dl-1, distinguishing between children from birth to day 7 (week 1), from day 8 to day 14 (week 2) or from day 15 (≥week 3) onwards. OBJECTIVE To observe peri-operative red blood cell transfusion practice according to guidelines in relation to patient outcome. DESIGN A multicentre observational study. SETTING The NEonate-Children sTudy of Anaesthesia pRactice IN Europe (NECTARINE) trial recruited patients up to 60 weeks' postmenstrual age undergoing anaesthesia for surgical or diagnostic procedures from 165 centres in 31 European countries between March 2016 and January 2017. PATIENTS The data included 5609 patients undergoing 6542 procedures. Inclusion criteria was a peri-operative red blood cell transfusion. MAIN OUTCOME MEASURES The primary endpoint was the haemoglobin level triggering a transfusion for neonates in week 1, week 2 and week 3. Secondary endpoints were transfusion volumes, 'delta haemoglobin' (preprocedure - transfusion-triggering) and 30-day and 90-day morbidity and mortality. RESULTS Peri-operative red blood cell transfusions were recorded during 447 procedures (6.9%). The median haemoglobin levels triggering a transfusion were 9.6 [IQR 8.7 to 10.9] g dl-1 for neonates in week 1, 9.6 [7.7 to 10.4] g dl-1 in week 2 and 8.0 [7.3 to 9.0] g dl-1 in week 3. The median transfusion volume was 17.1 [11.1 to 26.4] ml kg-1 with a median delta haemoglobin of 1.8 [0.0 to 3.6] g dl-1. Thirty-day morbidity was 47.8% with an overall mortality of 11.3%. CONCLUSIONS Results indicate lower transfusion-triggering haemoglobin thresholds in clinical practice than suggested by current guidelines. The high morbidity and mortality of this NECTARINE sub-cohort calls for investigative action and evidence-based guidelines addressing perioperative red blood cell transfusions strategies.
UR - http://www.scopus.com/inward/record.url?scp=85124056800&partnerID=8YFLogxK
U2 - 10.1097/EJA.0000000000001646
DO - 10.1097/EJA.0000000000001646
M3 - Article
C2 - 34845167
AN - SCOPUS:85124056800
SN - 0265-0215
VL - 39
SP - 252
EP - 260
JO - European Journal of Anaesthesiology
JF - European Journal of Anaesthesiology
IS - 3
ER -