Autoimmune heparin-induced thrombocytopenia and venous limb gangrene after aortic dissection repair: in vitro and in vivo effects of intravenous immunoglobulin

被引:22
作者
Arcinas, Liane A. [1 ]
Manji, Rizwan A. [2 ,3 ]
Hrymak, Carmen [3 ,4 ]
Dao, Vi [5 ]
Sheppard, Jo-Ann I. [6 ]
Warkentin, Theodore E. [6 ,7 ]
机构
[1] Univ Manitoba, Dept Internal Med, Winnipeg, MB, Canada
[2] Univ Manitoba, Sect Cardiac Surg, Dept Surg, Winnipeg, MB, Canada
[3] Univ Manitoba, Sect Crit Care, Dept Internal Med, Winnipeg, MB, Canada
[4] Univ Manitoba, Dept Emergency Med, Winnipeg, MB, Canada
[5] Univ Manitoba, Sect Hematol, Dept Internal Med, Winnipeg, MB, Canada
[6] McMaster Univ, Dept Pathol & Mol Med, Michael G DeGroote Sch Med, Hamilton, ON, Canada
[7] McMaster Univ, Dept Med, Michael G DeGroote Sch Med, Hamilton, ON, Canada
关键词
MOLECULAR-WEIGHT HEPARIN; PLATELET ACTIVATION; HIT; COMPLICATION; THROMBOSIS; GLOBULINS;
D O I
10.1111/trf.15263
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Heparin-induced thrombocytopenia (HIT) is a prothrombotic disorder characterized by heparin-dependent antibodies that activate platelets (PLTs) via PLT Fc gamma IIa receptors. "Autoimmune" HIT (aHIT) indicates a HIT subset where thrombocytopenia progresses or persists despite stopping heparin; aHIT sera activate PLTs strongly even in the absence of heparin (heparin-independent PLT-activating properties). Affected patients are at risk of severe complications, including dual macro- and microvascular thrombosis leading to venous limb gangrene. High-dose intravenous immunoglobulin (IVIG) offers an approach to interrupt heparin-independent PLT-activating effects of aHIT antibodies. CASE REPORT A 78-year-old male who underwent cardiopulmonary bypass for aortic dissection developed aHIT, disseminated intravascular coagulation, and deep vein thrombosis; progression to venous limb gangrene occurred during partial thromboplastin time (PTT)-adjusted bivalirudin infusion (underdosing from "PTT confounding"). Thrombocytopenia recovered with high-dose IVIG, although the PLT count increase began only after the third dose of a 5-day IVIG regimen (0.4 g/kg/day x 5 days). We reviewed case reports and case series of IVIG for treating HIT, focusing on various IVIG dosing regimens used. RESULTS Patient serum-induced PLT activation was inhibited in vitro by IVIG in a dose-dependent fashion; inhibition of PLT activation by IVIG was much more marked in the absence of heparin versus the presence of heparin (0.2 U/mL). Our literature review indicated 1 g/kg x 2 IVIG dosing as most common for treating HIT, usually associated with rapid PLT count recovery. CONCLUSION Our clinical and laboratory observations support dose-dependent efficacy of IVIG for decreasing PLT activation and thus correcting thrombocytopenia in aHIT. Our case experience and literature review suggests dosing of 1 g/kg IVIG x 2 for patients with severe aHIT.
引用
收藏
页码:1924 / 1933
页数:10
相关论文
共 41 条
[1]   Puerperal streptococcal toxic shock syndrome treated with recombinant human activated protein C and intravenous immunoglobulin [J].
Al-Rawi, S. ;
Woodward, L. J. ;
Knight, J. .
INTERNATIONAL JOURNAL OF OBSTETRIC ANESTHESIA, 2009, 18 (02) :169-172
[2]   Persistent Heparin-Induced Thrombocytopenia Treated With IVIg [J].
Azimov, Michelle B. ;
Slater, Evan D. .
CHEST, 2017, 152 (03) :679-680
[3]   Heparin-induced thrombocytopenia: correction of severe bleeding complication with intravenous immune globulin [J].
Betrosian, AP ;
Theodossiades, G ;
Balla, M ;
Diakalis, C ;
Georgiades, G .
INTENSIVE CARE MEDICINE, 2004, 30 (11) :2136-2136
[4]   Heparin-induced thrombocytopenia with pulmonary embolism and disseminated intravascular coagulation associated with low-molecular-weight heparin [J].
Betrosian, AP ;
Theodossiades, G ;
Lambroulis, G ;
Kostantonis, D ;
Balla, M ;
Papanikolaou, M ;
Georgiades, G .
AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 2003, 325 (01) :45-47
[5]   Potential role of intravenous immunoglobulin in the management of peripartum maternal thrombocytopenia due to various causes [J].
Cho, Fu-Nan ;
Liu, Cheng-Bin .
JOURNAL OF THE CHINESE MEDICAL ASSOCIATION, 2008, 71 (05) :267-269
[6]   Immune globulins and thrombotic adverse events as recorded in a large administrative database in 2008 through 2010 [J].
Daniel, Gregory W. ;
Menis, Mikhail ;
Sridhar, Gayathri ;
Scott, Dorothy ;
Wallace, Anna E. ;
Ovanesov, Mikhail V. ;
Golding, Basil ;
Anderson, Steven A. ;
Epstein, Jay ;
Martin, David ;
Ball, Robert ;
Izurieta, Hector S. .
TRANSFUSION, 2012, 52 (10) :2113-2121
[7]   Treatment of refractory delayed onset heparin-induced thrombocytopenia after thoracic endovascular aortic repair with intravenous immunoglobulin (IVIG) [J].
Doucette, Kimberley ;
DeStefano, Christin B. ;
Jain, Natasha A. ;
Cruz, Allan L. ;
Malkovska, Vera ;
Fitzpatrick, Kelly .
RESEARCH AND PRACTICE IN THROMBOSIS AND HAEMOSTASIS, 2017, 1 (01) :134-137
[8]   CORRECTION OF SEVERE HEPARIN-ASSOCIATED THROMBOCYTOPENIA WITH INTRAVENOUS IMMUNOGLOBULIN [J].
FRAME, JN ;
MULVEY, KP ;
PHARES, JC ;
ANDERSON, MJ .
ANNALS OF INTERNAL MEDICINE, 1989, 111 (11) :946-947
[9]   Cerebral Venous Sinus Thrombosis Due to Low-molecular-weight Heparin-induced Thrombocytopenia [J].
Gleichgerrcht, Ezequiel ;
Lim, Ming Y. ;
Turan, Tanya N. .
NEUROLOGIST, 2017, 22 (06) :241-244
[10]   HEPARIN-INDUCED THROMBOCYTOPENIA - RESPONSE TO INTRAVENOUS IMMUNOGLOBULIN INVIVO AND INVITRO [J].
GRAU, E ;
LINARES, M ;
OLASO, MA ;
RUVIRA, J ;
SANCHIS, J .
AMERICAN JOURNAL OF HEMATOLOGY, 1992, 39 (04) :312-313