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Impact of high-risk thrombophilia status on recurrence among children with a first non-central-venous-catheter-associated VTE: an observational multicentre cohort study
被引:22
|作者:
Limperger, Verena
[1
]
Kenet, Gili
[2
,3
]
Goldenberg, Neil A.
[4
,5
,6
]
Heller, Christine
[7
]
Holzhauer, Susanne
[8
]
Junker, Ralf
[1
]
Klostermeier, Ulrich C.
[1
]
Knoefler, Ralf
[9
]
Kurnik, Karin
[10
]
Kruempel, Anne
[11
]
Mesters, Rolf
[12
]
Stach, Michael
[13
]
Young, Guy
[14
]
Nowak-Goettl, Ulrike
[1
,11
]
机构:
[1] Univ Hosp Kiel, Inst Clin Chem, Kiel, Germany
[2] Natl Haemophilia Ctr, Thrombosis Unit, Tel Hashomer, Israel
[3] Tel Aviv Univ, Sackler Sch Med, Tel Aviv, Israel
[4] All Childrens Hosp Johns Hopkins Med, St Petersburg, FL USA
[5] All Childrens Res Inst, St Petersburg, FL USA
[6] Johns Hopkins Univ, Sch Med, Dept Pediat, Div Hematol, Baltimore, MD 21205 USA
[7] Dept Paediat Haemostaseol, Frankfurt, Germany
[8] Charite, Dept Paediat Haematol Oncol, Berlin, Germany
[9] Dept Paediat Haemostaseol, Dresden, Germany
[10] Univ Children Hosp Munich, Dept Paediat, Munich, Germany
[11] Univ Children Hosp Munster, Dept Paediat Haematol Oncol, Munster, Germany
[12] Univ Hosp Munster, Dept Med Haematol & Oncol, Munster, Germany
[13] Univ Hosp Munster, IT Serv Ctr, Munster, Germany
[14] Univ Southern Calif, Keck Sch Med, Childrens Hosp Los Angeles, Los Angeles, CA USA
关键词:
antithrombin;
children;
protein C pathway;
thrombophilia;
thrombosis;
PROTEIN-S DEFICIENCY;
INHERITED THROMBOPHILIA;
C-DEFICIENCY;
LABORATORY CHARACTERISTICS;
DEVELOPMENTAL HEMOSTASIS;
HEREDITARY DEFICIENCIES;
ANTICOAGULANT PATHWAY;
NUCLEOTIDE-SEQUENCE;
PULMONARY-EMBOLISM;
THROMBOEMBOLISM;
D O I:
10.1111/bjh.14192
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Deficiency of antithrombin (AT), protein C (PC) or protein S (PS) constitutes a major risk factor for venous thromboembolism (VTE). Individuals at high risk for recurrence who benefit from screening need to be identified. The primary study objective was to determine the individual recurrence risk among children with a first non-central-venous-catheter-associated VTE with respect to their thrombophilia status and to evaluate if the clinical presentation at first VTE onset differs between children with AT, PC or PS deficiency versus no thrombophilia. We calculated the absolute risk of VTE recurrence and event-free-survival adjusted for thrombophilia, age, sex and positive family VTE history in 161 consecutively enrolled paediatric VTE patients. The presence of a deficiency relative to no thrombophilia was evaluated as a potential predictor of recurrence. Predictors for recurrence were AT deficiency (hazard ratio/95% CI: 65/246-172) and female gender (26/11-635). The annual recurrence rates (95% CIs) were 54% (26-10) in AT-deficient children, 13% (03-38) in patients with PC deficiency, 07% (008-24) in the PS-deficient cohort and 09% (04-18) in patients with no thrombophilia. Positive family VTE history or combined thrombophilias did not predict recurrence. Given the overall annual incidence rate of recurrence of 15% we suggest screening for AT deficiency in children with VTE.
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页码:133 / 140
页数:8
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