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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
来源:
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.
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页码:1924 / 1933
页数:10
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