In vivo age dependency of unfractionated heparin in infants and children

被引:43
作者
Newall, Fiona [1 ,2 ]
Ignjatovic, Vera [1 ]
Summerhayes, Robyn [1 ]
Gan, Andrew
Butt, Warwick [3 ]
Johnston, Linda [2 ,4 ]
Monagle, Paul [1 ]
机构
[1] Univ Melbourne, Dept Pathol, Melbourne, Vic 3010, Australia
[2] Univ Melbourne, Sch Nursing & Social Work, Melbourne, Vic 3010, Australia
[3] Royal Childrens Hosp, Paediat Intens Care Unit, Brisbane, Qld, Australia
[4] Royal Childrens Hosp, Dept Neonatol, Brisbane, Qld, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
Unfractionated Heparin; Children; Anti-Xa; ETP; APTT; THERAPEUTIC RANGE; ASSAYS;
D O I
10.1016/j.thromres.2008.07.009
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Introduction: Unfractionated Heparin (UFH) is used widely in paediatrics. Paediatric specific recommendations for UFH therapy are few, with the majority of recommendations being extrapolated from adult practice. In vitro studies have shown that this practice may be suboptimal. This study aimed to improve the understanding of the impact of age upon UFH response in vivo. Materials and Methods: This prospective, observational study, conducted in the Paediatric Intensive Care Unit (PICU), included: patients 16 years or younger; treated with UFH of at least 10 U/Kg/hr. Laboratory analysis included: Antithrombin, APTT, Anti-Xa, Anti-IIa and thrombin generation expressed as the Endogenous Thrombin Potential. Results were grouped according to patient age (i.e. <1, 1-5, 6-10 and 11-16 years). Results: 85 patients received an equivalent mean UFH dose with a median duration of 3 days. Antithrombin levels were decreased compared to age-related norms in children up to 11 years of age. AMT results were comparable across the age-groups. The Anti-Xa results using two different assays showed a trend for lower values in younger children. All children less than one year old recorded Anti-Xa values outside the therapeutic range for heparin therapy, for both assays. There was a trend for decreased Anti-IIa activity in younger children. Endogenous Thrombin Potential showed a significant trend for increased inhibition in older children. In vitro Antithrombin supplementation did not change the Anti-Xa or thrombin generation. Conclusions: This study confirms that, in vivo, for the same dose of UFH, the anti Xa and anti IIa effect, as well as the inhibition of endogenous thrombin potential is age dependent and that these differences are not purely AT dependent. The implication is that the anticoagulant and antithrombotic effect of a given dose of UFH differs with age. Clinical outcome studies to determine the optimal dosing for each age group are warranted. Crown Copyright (C) 2008 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:710 / 714
页数:5
相关论文
共 19 条
[1]
HEPARIN CLEARANCE AND EX VIVO RECOVERY IN NEWBORN PIGLETS AND ADULT-PIGS [J].
ANDREW, M ;
OFOSU, F ;
SCHMIDT, B ;
BROOKER, L ;
HIRSH, J ;
BUCHANAN, MR .
THROMBOSIS RESEARCH, 1988, 52 (06) :517-527
[2]
Inability of the activated partial thromboplastin time to predict heparin levels - Time to reassess guidelines for heparin assays [J].
Baker, BA ;
Adelman, MD ;
Smith, PA ;
Osborn, JC .
ARCHIVES OF INTERNAL MEDICINE, 1997, 157 (21) :2475-2479
[3]
A549 LUNG EPITHELIAL-CELLS SYNTHESIZE ANTICOAGULANT MOLECULES ON THE CELL-SURFACE AND MATRIX AND IN CONDITIONED MEDIA [J].
BERRY, L ;
ANDREW, M ;
POST, M ;
OFOSU, F ;
OBRODOVICH, H .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1991, 4 (04) :338-346
[4]
ESTABLISHING A THERAPEUTIC RANGE FOR HEPARIN-THERAPY [J].
BRILLEDWARDS, P ;
GINSBERG, JS ;
JOHNSTON, M ;
HIRSH, J .
ANNALS OF INTERNAL MEDICINE, 1993, 119 (02) :104-109
[5]
COMPARISON OF ACTIVATED COAGULATION LIME AND WHOLE-BLOOD HEPARIN MEASUREMENTS WITH LABORATORY PLASMA ANTI-XA HEPARIN CONCENTRATION IN PATIENTS HAVING CARDIAC OPERATIONS [J].
DESPOTIS, GJ ;
SUMMERFIELD, AL ;
JOIST, JH ;
GOODNOUGH, LT ;
SANTORO, SA ;
SPITZNAGEL, E ;
COX, JL ;
LAPPAS, DG .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 1994, 108 (06) :1076-1082
[6]
Heparin and low-molecular-weight heparin - The Seventh ACCP Conference on Antithrombotic and Thrombolytic Therapy [J].
Hirsh, J ;
Raschke, R .
CHEST, 2004, 126 (03) :188S-203S
[7]
Thrombin generation: the functional role of alpha-2-macroglobulin and influence of developmental haemostasis [J].
Ignjatovic, V. ;
Greenway, A. ;
Summerhayes, R. ;
Monagle, P. .
BRITISH JOURNAL OF HAEMATOLOGY, 2007, 138 (03) :366-368
[8]
Therapeutic range for unfractionated heparin therapy: age-related differences in response in children [J].
Ignjatovic, V. ;
Summerhayes, R. ;
Than, J. ;
Gan, A. ;
Monagle, P. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2006, 4 (10) :2280-2283
[9]
Monitoring unfractionated heparin (UFH) therapy: Which anti factor Xa assay is appropriate? [J].
Ignjatovic, Vera ;
Summerhayes, Robyn ;
Gan, Andrew ;
Than, Jenny ;
Chan, Anthony ;
Cochrane, Andrew ;
Bennett, Martin ;
Horton, Stephen ;
Shann, Frank ;
Lane, Geoff ;
Ross-Smith, Maree ;
Monagle, Paul .
THROMBOSIS RESEARCH, 2007, 120 (03) :347-351
[10]
Age-related differences in heparin response [J].
Ignjatovic, Vera ;
Furmedge, Janine ;
Newall, Fiona ;
Chan, Anthony ;
Berry, Leslie ;
Fong, Chrystal ;
Cheng, Ken ;
Monagle, Paul .
THROMBOSIS RESEARCH, 2006, 118 (06) :741-745