Transfusion-associated hazards: A revisit of their presentation

被引:29
|
作者
Garraud, O. [1 ,2 ]
Sut, C. [1 ]
Haddad, A. [1 ,3 ]
Tariket, S. [1 ]
Aloui, C. [1 ]
Laradi, S. [1 ,3 ]
Hamzeh-Cognasse, H. [1 ]
Bourlet, T. [1 ,4 ]
Zeni, F. [1 ,5 ]
Aubron, C. [6 ,7 ]
Ozier, Y. [6 ,7 ]
Laperche, S. [2 ]
Peyrard, T. [2 ,8 ]
Buffet, P. [2 ,8 ,9 ]
Guyotat, D. [10 ,11 ]
Tavernier, E. [10 ,11 ]
Cognasse, F. [1 ,3 ]
Pozzetto, B. [1 ,4 ]
Andreu, G. [2 ]
机构
[1] Lyon Univ St Etienne, EA3064, St Etienne, France
[2] Inst Natl Transfus Sanguine, F-75017 Paris, France
[3] Sacre Caeur Univ Hosp, Beirut, Lebanon
[4] Univ Hosp, Dept Microbiol, F-42023 St Etienne, France
[5] Univ Hosp, Dept Crit Care, F-29200 St Etienne, France
[6] Univ Bretagne Occidentale, F-29200 Brest, France
[7] Univ Hosp, Dept Crit Care, F-75005 Brest, France
[8] INSERM, S 1134, F-75015 Paris, France
[9] Univ Paris 05, Paris, France
[10] Univ Lyon, UMR 5229, F-69675 Lyon, France
[11] Inst Canc Lucien Neuwirth, F-42023 St Etienne, France
关键词
Transfusion; Adverse reactions; Hemovigilance; Prevention; Safety; ACUTE LUNG INJURY; CREUTZFELDT-JAKOB-DISEASE; RED-BLOOD-CELLS; VERSUS-HOST-DISEASE; SOLUBLE CD40 LIGAND; ADVERSE-REACTIONS; CIRCULATORY OVERLOAD; PATHOGEN INACTIVATION; RISK-FACTORS; HUMAN CYTOMEGALOVIRUS;
D O I
10.1016/j.tracli.2018.03.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
As a therapy or a support to other therapies, despite being largely beneficial to patients in general, transfusion it is not devoid of some risks. In a moderate number of cases, patients may manifest adverse reactions, otherwise referred to as transfusion-associated hazards (TAHs). The latest French 2016 haemovigilance report indicates that 93% of TAHs are minor (grade 1), 5.5% are moderate (grade 2) and 1.6% are severe (grade 3), with only five deaths (grade 4) being attributed to transfusion with relative certainty (imputability of level [or grade] 1 to 3). Health-care providers need to be well aware of the benefits and potential risks (to best evaluate and discuss the benefit risk ratio), how to prevent TAHs, the overall costs and the availability of alternative therapeutic options. In high-income countries, most blood establishments (BEs) and hospital blood banks (HBBs) have developed tools for reporting and analysing at least severe transfusion reactions. With nearly two decades of haemovigilance, transfusion reaction databases should be quite informative, though there are four main caveats that prevent it from being fully efficient: (ai) reporting is mainly declarative and is thus barely exhaustive even in countries where it is mandatory by law; (aii) it is often difficult to differentiate between the different complications related to transfusion, diseases, comorbidities and other types of therapies in patients suffering from debilitating conditions; (aiii) there is a lack of consistency in the definitions used to describe and report some transfusion reactions, their severity and their likelihood of being related to transfusion; and (aiv) it is difficult to assess the imputability of a particular BC given to a patient who has previously received many BCs over a relatively short period of time. When compiling all available information published so far, it appears that TAHs can be analysed using different approaches: (bi) their pathophysiological nature; (bii) their severity; (biii) the onset scheme; (biv) a quality assessment (preventable or non-preventable); (bv) their impact on ongoing therapy. Moreover, TAHs can be reported either in a non-integrative or in an integrative way; in the latter case, presentation may also differ when issued by a blood establishment or a treating ward. At some point, a recapitulative document would be useful to gain a better understanding of TAHs in order to decrease their occurrence and severity and allow decision makers to determine action plans: this is what this review attempts to make. This review attempts to merge the different aspects, with a focus on the hospital side, i.e., how the most frequent TAHs can be avoided or mitigated. (C) 2018 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:118 / 135
页数:18
相关论文
共 50 条
  • [1] Clinical Presentation and Treatment of Transfusion-Associated Babesiosis in Premature Infants
    Simonsen, Kari A.
    Harwell, Joseph I.
    Lainwala, Shabnam
    PEDIATRICS, 2011, 128 (04) : E1019 - E1024
  • [2] Transfusion-associated microchimerism
    Utter, G. H.
    Reed, W. F.
    Lee, T.-H.
    Busch, M. P.
    VOX SANGUINIS, 2007, 93 (03) : 188 - 195
  • [3] Transfusion-Associated Hyperkalemia
    Vraets, Adrienne
    Lin, Yulia
    Callum, Jeannie L.
    TRANSFUSION MEDICINE REVIEWS, 2011, 25 (03) : 184 - 196
  • [4] TRANSFUSION-ASSOCIATED AIDS
    PERKINS, HA
    AMERICAN JOURNAL OF HEMATOLOGY, 1985, 19 (03) : 307 - 313
  • [5] TRANSFUSION-ASSOCIATED MALARIA
    CAMAZINE, B
    LANCET, 1985, 2 (8445): : 37 - 37
  • [6] TRANSFUSION-ASSOCIATED VIRAL HEPATITIS
    MOSLEY, JW
    DULL, HB
    ANESTHESIOLOGY, 1966, 27 (04) : 409 - &
  • [7] TRANSFUSION-ASSOCIATED CYTOMEGALOVIRUS INFECTIONS
    ADLER, SP
    REVIEWS OF INFECTIOUS DISEASES, 1983, 5 (06): : 977 - 993
  • [8] REPORTING TRANSFUSION-ASSOCIATED HEPATITIS
    GRINDON, AJ
    ROSVOLL, RV
    TRANSFUSION, 1980, 20 (01) : 108 - 109
  • [9] A TRANSFUSION-ASSOCIATED CASE OF BABESIOSIS
    Washburn, R.
    Ong, M.
    Nanchahal, D.
    Todd, J.
    Cotelingham, J.
    Rafeek, H.
    JOURNAL OF INVESTIGATIVE MEDICINE, 2017, 65 (02) : 497 - 497
  • [10] Transfusion-associated circulatory overload
    Ozier, Y.
    Mouquet, F.
    Rieux, C.
    Mertes, P. -M.
    Muller, J. -Y.
    Caldani, C.
    Boudjedir, K.
    Carlier, M.
    TRANSFUSION CLINIQUE ET BIOLOGIQUE, 2012, 19 (4-5) : 263 - 269