TY - JOUR
T1 - Preoperative intravenous iron before cardiac surgery
T2 - a prospective multicentre feasibility study
AU - Klein, Andrew A.
AU - Chau, Marisa
AU - Yeates, James A.
AU - Collier, Timothy
AU - Evans, Caroline
AU - Agarwal, Seema
AU - Richards, Toby
AU - on behalf of the UK Cardiac and Vascular Surgery Interventional Anaemia Response (CAVIAR) study team
N1 - Funding Information:
Funded by a grant from the Association of Cardiothoracic Anaesthesia and Critical Care (ACTACC) , the Vascular Anaesthesia Society of Great Britain and Ireland , and the British Journal of Anaesthesia , via the National Institute of Academic Anaesthesia . Additional funding for staff resources was provided by Pharmacosmos. The study was included in the NIHR Portfolio and the NIHR provided additional funds to the study centres for assistance with patient recruitment. None of the funders had any influence on study design, trial management, analysis of the data, preparation of the manuscript, or decision to submit. Appendix 1 CAVIAR investigators by site. Appendix 1: Royal Free Hospital Daniel Martin Papworth Hospital Andrew Klein(PI) and James Yeates Cardiff (University Hospital of Wales) Caroline Evans Liverpool Hospital Seema Agarwal Freeman Hospital Michael Clarke Royal Infirmary of Edinburgh Peter Alston Castle Hill Hospital Ajith Vijayan Manchester Royal Infirmary Akbar Vohra Essex Cardiothoracic Centre Anirudda Pai Brighton & Sussex University Hospitals Anita Sugavanam Guy's & St. Thomas Hospital Jugdeep Dhesi Royal Oldham Hospital Damian Kelleher Royal Cornwall Hospital Harvey Chant Royal Blackpool Hospital Palanikumar Saravanan Royal Bournemouth Hospital Richard Green University Hospitals of Leicester Matthew Bown Derriford Hospital Mark Bennett King's College Hospital Gudrun Kunst James Cook University Hospital Adrian Mellor Appendix A
Funding Information:
AK or his institution has received educational grant funding, honoraria or travel expenses from Pharmacosmos , Vifor Pharma , Massimo , Hemonetics , Hemosonics , and Fisher and Paykel . MC's salary is supported by Pharmacosmos. CE has undertaken consulting work for Pharmacosmos. SA has received research funding and honoraria from Pharmacosmos . TR reports grants, personal fees, and non-financial support from Pharmacosmos ; grants, personal fees, and non-financial support from Vifor Pharma ; grants, personal fees, and non-financial support from Acelity ; grants, personal fees, and non-financial support from Stroke Association ; grants from Mason Medical Research Foundation ; grants from UCH league of Friends; and grants and non-financial support from Libresse/Bodyform .
Funding Information:
AK or his institution has received educational grant funding, honoraria or travel expenses from Pharmacosmos, Vifor Pharma, Massimo, Hemonetics, Hemosonics, and Fisher and Paykel. MC's salary is supported by Pharmacosmos. CE has undertaken consulting work for Pharmacosmos. SA has received research funding and honoraria from Pharmacosmos. TR reports grants, personal fees, and non-financial support from Pharmacosmos; grants, personal fees, and non-financial support from Vifor Pharma; grants, personal fees, and non-financial support from Acelity; grants, personal fees, and non-financial support from Stroke Association; grants from Mason Medical Research Foundation; grants from UCH league of Friends; and grants and non-financial support from Libresse/Bodyform.Funded by a grant from the Association of Cardiothoracic Anaesthesia and Critical Care (ACTACC), the Vascular Anaesthesia Society of Great Britain and Ireland, and the British Journal of Anaesthesia, via the National Institute of Academic Anaesthesia. Additional funding for staff resources was provided by Pharmacosmos. The study was included in the NIHR Portfolio and the NIHR provided additional funds to the study centres for assistance with patient recruitment. None of the funders had any influence on study design, trial management, analysis of the data, preparation of the manuscript, or decision to submit.
Publisher Copyright:
© 2019 British Journal of Anaesthesia
PY - 2020/3
Y1 - 2020/3
N2 - Background: Preoperative anaemia affects one third of patients undergoing cardiac surgery and is associated with increased mortality and morbidity. Although it is recommended that perioperative teams should identify and treat patients with preoperative anaemia before surgery, introducing new treatment protocols can be challenging in surgical pathways. The aim of this study was to assess the feasibility and effectiveness of introducing a preoperative intravenous iron service as a national initiative in cardiac surgery. Methods: We performed a multicentre, stepped, observational study using the UK Association of Cardiothoracic Anaesthesia and Critical Care Research Network. The primary feasibility outcome was the ability to set up an anaemia and intravenous iron clinic at each site. The primary efficacy outcome was change in haemoglobin (Hb) concentration between intervention and operation. Secondary outcomes included blood transfusion and hospital stay. Patients with anaemia were compared with non-anaemic patients and with those who received intravenous iron as part of their routine treatment protocol. Results: Seven out of 11 NHS hospitals successfully set up iron clinics over 2 yr, and 228 patients were recruited into this study. Patients with anaemia who received intravenous iron were at higher surgical risk, were more likely to have a known previous history of iron deficiency or anaemia, had a higher rate of chronic kidney disease, and were slightly more anaemic than the non-treated group. Intravenous iron was administered a median (inter-quartile range, IQR [range]) of 33 (15–53 [4–303]) days before surgery. Preoperative intravenous iron increased [Hb] from baseline to pre-surgery; mean (95% confidence interval) change was +8.4 (5.0–11.8) g L−1 (P<0.001). Overall, anaemic compared with non-anaemic patients were more likely to be transfused (49% [59/136] vs 27% (22/92), P=0.001) and stayed longer in hospital (median days [IQR], 9 [7–15] vs 8 [6–11]; P=0.014). The number of days alive and at home was lower in the anaemic group (median days [IQR], 20 [14–22] vs 21 [17–23]; P=0.033). Conclusion: The development of an intravenous iron pathway is feasible but appears limited to selected high-risk cardiac patients in routine NHS practise. Although intravenous iron increased [Hb], there is a need for an appropriately powered clinical trial to assess the clinical effect of intravenous iron on patient-centred outcomes.
AB - Background: Preoperative anaemia affects one third of patients undergoing cardiac surgery and is associated with increased mortality and morbidity. Although it is recommended that perioperative teams should identify and treat patients with preoperative anaemia before surgery, introducing new treatment protocols can be challenging in surgical pathways. The aim of this study was to assess the feasibility and effectiveness of introducing a preoperative intravenous iron service as a national initiative in cardiac surgery. Methods: We performed a multicentre, stepped, observational study using the UK Association of Cardiothoracic Anaesthesia and Critical Care Research Network. The primary feasibility outcome was the ability to set up an anaemia and intravenous iron clinic at each site. The primary efficacy outcome was change in haemoglobin (Hb) concentration between intervention and operation. Secondary outcomes included blood transfusion and hospital stay. Patients with anaemia were compared with non-anaemic patients and with those who received intravenous iron as part of their routine treatment protocol. Results: Seven out of 11 NHS hospitals successfully set up iron clinics over 2 yr, and 228 patients were recruited into this study. Patients with anaemia who received intravenous iron were at higher surgical risk, were more likely to have a known previous history of iron deficiency or anaemia, had a higher rate of chronic kidney disease, and were slightly more anaemic than the non-treated group. Intravenous iron was administered a median (inter-quartile range, IQR [range]) of 33 (15–53 [4–303]) days before surgery. Preoperative intravenous iron increased [Hb] from baseline to pre-surgery; mean (95% confidence interval) change was +8.4 (5.0–11.8) g L−1 (P<0.001). Overall, anaemic compared with non-anaemic patients were more likely to be transfused (49% [59/136] vs 27% (22/92), P=0.001) and stayed longer in hospital (median days [IQR], 9 [7–15] vs 8 [6–11]; P=0.014). The number of days alive and at home was lower in the anaemic group (median days [IQR], 20 [14–22] vs 21 [17–23]; P=0.033). Conclusion: The development of an intravenous iron pathway is feasible but appears limited to selected high-risk cardiac patients in routine NHS practise. Although intravenous iron increased [Hb], there is a need for an appropriately powered clinical trial to assess the clinical effect of intravenous iron on patient-centred outcomes.
KW - anaemia
KW - cardiac surgery
KW - haemoglobin
KW - intravenous iron
KW - iron deficiency
KW - outcome
KW - preoperative
KW - transfusion
UR - http://www.scopus.com/inward/record.url?scp=85077356377&partnerID=8YFLogxK
U2 - 10.1016/j.bja.2019.11.023
DO - 10.1016/j.bja.2019.11.023
M3 - Article
C2 - 31902590
AN - SCOPUS:85077356377
SN - 0007-0912
VL - 124
SP - 243
EP - 250
JO - British Journal of Anaesthesia
JF - British Journal of Anaesthesia
IS - 3
ER -