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2.
Stroke ; 50(3): e51-e96, 2019 03.
Article in English | MEDLINE | ID: mdl-30686119

ABSTRACT

Purpose- Much has transpired since the last scientific statement on pediatric stroke was published 10 years ago. Although stroke has long been recognized as an adult health problem causing substantial morbidity and mortality, it is also an important cause of acquired brain injury in young patients, occurring most commonly in the neonate and throughout childhood. This scientific statement represents a synthesis of data and a consensus of the leading experts in childhood cardiovascular disease and stroke. Methods- Members of the writing group were appointed by the American Heart Association Stroke Council's Scientific Statement Oversight Committee and the American Heart Association's Manuscript Oversight Committee and were chosen to reflect the expertise of the subject matter. The writers used systematic literature reviews, references to published clinical and epidemiology studies, morbidity and mortality reports, clinical and public health guidelines, authoritative statements, personal files, and expert opinion to summarize existing evidence and to indicate gaps in current knowledge. This scientific statement is based on expert consensus considerations for clinical practice. Results- Annualized pediatric stroke incidence rates, including both neonatal and later childhood stroke and both ischemic and hemorrhagic stroke, range from 3 to 25 per 100 000 children in developed countries. Newborns have the highest risk ratio: 1 in 4000 live births. Stroke is a clinical syndrome. Delays in diagnosis are common in both perinatal and childhood stroke but for different reasons. To develop new strategies for prevention and treatment, disease processes and risk factors that lead to pediatric stroke are discussed here to aid the clinician in rapid diagnosis and treatment. The many important differences that affect the pathophysiology and treatment of childhood stroke are discussed in each section. Conclusions- Here we provide updates on perinatal and childhood stroke with a focus on the subtypes, including arterial ischemic, venous thrombotic, and hemorrhagic stroke, and updates in regard to areas of childhood stroke that have not received close attention such as sickle cell disease. Each section is highlighted with considerations for clinical practice, attendant controversies, and knowledge gaps. This statement provides the practicing provider with much-needed updated information in this field.


Subject(s)
Stroke/therapy , Adolescent , American Heart Association , Association , Brain Ischemia/epidemiology , Brain Ischemia/therapy , Child , Child, Preschool , Humans , Incidence , Infant , Infant, Newborn , Pediatrics , Stroke/epidemiology , United States
3.
Blood ; 129(20): 2793-2800, 2017 05 18.
Article in English | MEDLINE | ID: mdl-28258054

ABSTRACT

Perinatal stroke causes cerebral palsy and lifelong disability. Specific diseases are definable, but mechanisms are poorly understood. Evidence suggests possible associations between arterial perinatal stroke and prothrombotic disorders, but population-based, controlled, disease-specific studies are limited. Understanding thrombophilia in perinatal stroke informs pathogenesis models and clinical management. We conducted a population-based, prospective, case-control study to determine the association of specific perinatal stroke diseases with known thrombophilias. Children with idiopathic magnetic resonance imaging-classified neonatal arterial ischemic stroke (NAIS), arterial presumed perinatal ischemic stroke (APPIS), or fetal periventricular venous infarction (PVI) were recruited. Standardized thrombophilia evaluations were performed after 12 months of age on stroke cases and controls, including quantified proteins C and S, antithrombin, factors VIII/IX/XI, fibrinogen, lipoprotein(a), homocysteine, lupus anticoagulant, anticardiolipin antibodies and genotyping of factor V Leiden (FVL), factor II G20210A (FII), and methylenetetrahydrofolate reductase C677T. A total of 212 children were studied: 46 with NAIS, 34 with APPIS, 55 with PVI, and 77 controls (male, 53%; median age, 4.8 years). Of 14 parameters, no differences were observed in 12, including all common thrombophilias. Mean prothrombin time was shorter in arterial strokes (P < .001). Rates of antiphospholipid antibodies were low, comparable to those in controls, and resolved on repeat testing. FVL and FII rates were comparable to population norms. Total number of possible abnormalities did not differ between cases and controls. Our prospective, population-based, controlled, disease-specific study suggests minimal association between perinatal stroke and thrombophilia. This does not exclude the possibility of disordered coagulation at the time of stroke but suggests testing in childhood is not indicated.


Subject(s)
Stroke/complications , Thrombophilia/epidemiology , Thrombophilia/etiology , Adolescent , Child , Child, Preschool , Female , Genotype , Humans , Infant , Infant, Newborn , Male , Risk Factors , Thrombophilia/genetics , Young Adult
4.
Am Heart J ; 162(3): 425-35.e6, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21884857

ABSTRACT

BACKGROUND: Currently, there are no Food and Drug Administration-approved devices available that can provide long-term mechanical circulatory support to smaller children with severe heart failure as a bridge to heart transplant (HT). In recent years, the Berlin Heart EXCOR Pediatric ventricular assist device (VAD) has emerged as a potential treatment option. Systematic data on the safety and efficacy of the EXCOR are limited. METHODS: The Investigational Device Exemption (IDE) clinical study is designed to evaluate the safety and probable benefit of the EXCOR to support regulatory review of the device under the Humanitarian Device Exemption regulation. The study design and rationale are reviewed in light of the well-described challenges inherent in small population studies. RESULTS: The Berlin Heart EXCOR IDE clinical study is a prospective, multicenter, single-arm, clinical cohort study. Children aged 0 to 16 years with severe heart failure (Interagency Registry for Mechanically Assisted Circulatory Support profile 1 or 2) due to 2-ventricle heart disease and actively listed for HT comprise the primary study cohort. The control population is a propensity-matched retrospective cohort of children supported with extracorporeal membrane oxygenation, the only bridge device available to smaller children before the EXCOR. The primary efficacy end point is survival to heart transplantation or recovery. The primary safety end point is the incidence of serious adverse events as defined by pediatric Interagency Registry for Mechanically Assisted Circulatory Support criteria. The study will enroll a total of 48 subjects in 2 cohorts based on body surface area (cohort 1 <0.7 m(2), cohort 2 0.7-1.5 m(2)) and is powered to show safety superiority to a prespecified performance goal of 0.25 serious adverse events per day of support. Children ineligible for the primary cohort will still have access to the device in a third compassionate-use cohort where adverse event data will be collected for additional safety characterization of the device. CONCLUSION: The Berlin Heart IDE clinical study will be the first bridge-to-HT VAD study designed exclusively for children. It is anticipated that the study will provide important information on the safety and efficacy of the Berlin Heart EXCOR Pediatric in children while providing valuable lessons into the design and conduct of future VAD studies in children.


Subject(s)
Heart Failure/therapy , Heart-Assist Devices , Preoperative Care/instrumentation , Recovery of Function/physiology , Ventricular Function/physiology , Adolescent , Child , Child, Preschool , Extracorporeal Membrane Oxygenation , Female , Follow-Up Studies , Heart Failure/diagnosis , Heart Failure/physiopathology , Heart Transplantation , Humans , Infant , Infant, Newborn , Male , Prospective Studies , Single-Blind Method , Treatment Outcome
5.
Semin Fetal Neonatal Med ; 16(6): 294-300, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21872543

ABSTRACT

The haemostatic system is a complex interaction between the vasculature, cellular components and plasma proteins that interact to maintain haemostasis in the healthy body. The haemostatic system can be further defined as primary, secondary and tertiary haemostasis to better define the interdependent mechanisms that combine to maintain haemostasis. The term 'developmental haemostasis' was first introduced by Maureen Andrews in the 1980s to describe the age-related physiological changes of the coagulation system as it develops progressively over time from fetal, neonatal, paediatric to adult and geriatric systems. This paper will focus on developmental changes in secondary haemostasis, that is, the plasma protein changes that occur with age, particularly during the fetal and neonatal period, when the changes are most marked compared to the adult system.


Subject(s)
Blood Coagulation Factors/physiology , Blood Coagulation/physiology , Fetal Development/physiology , Blood Coagulation Tests , Fetus , Hemostasis/physiology , Humans , Infant, Newborn
6.
J Thorac Cardiovasc Surg ; 136(6): 1442-9, 2008 Dec.
Article in English | MEDLINE | ID: mdl-19114187

ABSTRACT

OBJECTIVE: This study compared the effects of reconstituted fresh whole blood against standard blood component therapy in neonates undergoing cardiac surgery. METHODS: Patients less than 1 month of age were randomized to receive either reconstituted fresh whole blood (n = 31) or standard blood component therapy (n = 33) to prime the bypass circuit and for transfusion during the 24 hours after cardiopulmonary bypass. Primary outcome was chest tube drainage; secondary outcomes included transfusion needs, inotrope score, ventilation time, and hospital length of stay. RESULTS: Patients who received reconstituted fresh whole blood had significantly less postoperative chest tube volume loss per kilogram of body weight (7.7 mL/kg vs 11.8 mL/kg; P = .03). Standard blood component therapy was associated with higher inotropic score (6.6 vs 3.3; P = .002), longer ventilation times (164 hours vs 119 hours; P = .04), as well as longer hospital stays (18 days vs 12 days; P = .006) than patients receiving reconstituted fresh whole blood. Of the different factors associated with the use of reconstituted fresh whole blood, lower platelet counts at 10 minutes and at the end of cardiopulmonary bypass, older age of cells used in the prime and throughout bypass, and exposures to higher number of allogeneic donors were found to be independent predictors of poor clinical outcomes. CONCLUSIONS: Reconstituted fresh whole blood used for the prime, throughout cardiopulmonary bypass, and for all transfusion requirements within the first 24 hours postoperatively results in reduced chest tube volume loss and improved clinical outcomes in neonatal patients undergoing cardiac surgery.


Subject(s)
Blood Transfusion/methods , Cardiac Surgical Procedures , Heart Defects, Congenital/surgery , Transfusion Reaction , Blood Component Transfusion/adverse effects , Cardiopulmonary Bypass , Double-Blind Method , Female , Humans , Infant, Newborn , Male , Prospective Studies , Treatment Outcome
7.
Chest ; 133(6 Suppl): 887S-968S, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18574281

ABSTRACT

This chapter about antithrombotic therapy in neonates and children is part of the Antithrombotic and Thrombolytic Therapy: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines (8th Edition). Grade 1 recommendations are strong and indicate that the benefits do, or do not, outweigh risks, burden, and costs, and Grade 2 suggests that individual patient values may lead to different choices (for a full understanding of the grading, see Guyatt et al in this supplement, pages 123S-131S). In this chapter, many recommendations are based on extrapolation of adult data, and the reader is referred to the appropriate chapters relating to guidelines for adult populations. Within this chapter, the majority of recommendations are separate for neonates and children, reflecting the significant differences in epidemiology of thrombosis and safety and efficacy of therapy in these two populations. Among the key recommendations in this chapter are the following: In children with first episode of venous thromboembolism (VTE), we recommend anticoagulant therapy with either unfractionated heparin (UFH) or low-molecular-weight heparin (LMWH) [Grade 1B]. Dosing of IV UFH should prolong the activated partial thromboplastin time (aPTT) to a range that corresponds to an anti-factor Xa assay (anti-FXa) level of 0.35 to 0.7 U/mL, whereas LMWH should achieve an anti-FXa level of 0.5 to 1.0 U/mL 4 h after an injection for twice-daily dosing. In neonates with first VTE, we suggest either anticoagulation or supportive care with radiologic monitoring and subsequent anticoagulation if extension of the thrombosis occurs during supportive care (Grade 2C). We recommend against the use of routine systemic thromboprophylaxis for children with central venous lines (Grade 1B). For children with cerebral sinovenous thrombosis (CSVT) without significant intracranial hemorrhage (ICH), we recommend anticoagulation initially with UFH, or LMWH and subsequently with LMWH or vitamin K antagonists (VKAs) for a minimum of 3 months (Grade 1B). For children with non-sickle-cell disease-related acute arterial ischemic stroke (AIS), we recommend UFH or LMWH or aspirin (1 to 5 mg/kg/d) as initial therapy until dissection and embolic causes have been excluded (Grade 1B). For neonates with a first AIS, in the absence of a documented ongoing cardioembolic source, we recommend against anticoagulation or aspirin therapy (Grade 1B).


Subject(s)
Fibrinolytic Agents/therapeutic use , Heparin, Low-Molecular-Weight/therapeutic use , Venous Thrombosis/drug therapy , Aspirin/administration & dosage , Aspirin/therapeutic use , Child , Drug Therapy, Combination , Heparin, Low-Molecular-Weight/administration & dosage , Humans , Infant, Newborn , Partial Thromboplastin Time , Risk Assessment , Risk Factors , Vitamin K/antagonists & inhibitors
8.
Front Neurol Neurosci ; 23: 122-31, 2008.
Article in English | MEDLINE | ID: mdl-18004058

ABSTRACT

Cerebral venous thrombosis is currently thought to be a relatively rare and benign entity in childhood. Recent studies however have shown that cerebral venous thrombosis is more common than previously believed, and carries significant mortality and neurologic morbidity. Neonates are the most commonly affected age group, compared to children >1 month of age. Magnetic resonance imaging venography is the gold standard by which this diagnosis should be made. Clinical trials are currently necessary to determine the most efficacious,safe, and age-specific approach for anticoagulation for this childhood disorder.


Subject(s)
Cerebral Veins/pathology , Intracranial Thrombosis , Pediatrics , Child, Preschool , Humans , Infant , Infant, Newborn , Intracranial Thrombosis/diagnosis , Intracranial Thrombosis/physiopathology , Intracranial Thrombosis/therapy
9.
Haematologica ; 92(4): 554-7, 2007 Apr.
Article in English | MEDLINE | ID: mdl-17488668

ABSTRACT

UNLABELLED: The activated partial thromboplastin time (aPTT) and anti-Xa activity are used for monitoring unfractionated heparin (UFH) therapy in children and may not be optimal. OBJECTIVE: Determine correlations of aPTT, anti-Xa and UFH dose in children. Single centre prospective cohort study in children receiving UFH. The aPTT and anti-Xa results from routine coagulation monitoring were collected. Thirty-nine children (median age 18 days) were enrolled. There was no relationship between aPTT and UFH dose (r2=0.12) or anti-Xa and UFH dose (r2=0.03) or aPTT and anti-Xa (r2=0.22). aPTT and anti-Xa do not accurately monitor UFH therapy in children.


Subject(s)
Anticoagulants/administration & dosage , Blood Coagulation Tests , Critical Care/methods , Factor Xa Inhibitors , Heparin/administration & dosage , Adolescent , Anticoagulants/adverse effects , Anticoagulants/pharmacology , Anticoagulants/therapeutic use , Child , Child, Preschool , Cohort Studies , Dose-Response Relationship, Drug , Drug Monitoring , Female , Heart Defects, Congenital/blood , Hemorrhage/chemically induced , Heparin/adverse effects , Heparin/pharmacology , Heparin/therapeutic use , Humans , Infant , Infant, Newborn , Male , Partial Thromboplastin Time , Postoperative Complications/prevention & control , Prospective Studies , Pulmonary Embolism/drug therapy , Thrombin , Thrombophilia/drug therapy , Thrombosis/prevention & control , Venous Thrombosis/drug therapy
10.
Haematologica ; 92(2): 244-7, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17296576

ABSTRACT

Unfractionated heparin (UFH) is frequently prescribed for children for the prevention and treatment of thrombosis; however, its safety and efficacy have not been assessed. The aim of this single center, prospective cohort study was to determine the incidence of major bleeding and recurrent thrombosis in children receiving UFH. Major bleeding was defined a priori as: central nervous system or retroperitoneal bleeding, bleeding resulting in UFH being stopped or overt bleeding causing a drop in hemoglobin >20 g/dL in less than 24 h. Major bleeding events occurred in 9/38 children (24%, 95% CI 11-40%) and 2/38 (5%, 95% CI 0-18%) developed thrombosis. In conclusion, there is clinically significant bleeding in children receiving UFH.


Subject(s)
Hemorrhage/chemically induced , Hemorrhage/epidemiology , Heparin/therapeutic use , Thrombosis/drug therapy , Adolescent , Anticoagulants/therapeutic use , Child , Child, Preschool , Cohort Studies , Female , Hemoglobins/biosynthesis , Humans , Infant , Infant, Newborn , Male , Prospective Studies , Treatment Outcome
11.
Acta Paediatr ; 95(9): 1049-52, 2006 Sep.
Article in English | MEDLINE | ID: mdl-16938748

ABSTRACT

UNLABELLED: Approximately one third of children with malignancy and central venous lines develop catheter-related thrombosis, with the reported sequelae including death, pulmonary embolism, chylothoraces, superior vena cava syndrome and post-thrombotic syndrome. These complications prompt the design and completion of randomized, controlled trials to determine a safe and efficacious therapy to prevent these thromboses. The authors Ruud et al. have presented a well-designed, randomized, controlled trial which demonstrates the lack of utility of using low-dose warfarin to prevent catheter-related thrombosis in children with central lines and acute lymphoblastic leukaemia. The difficulties with warfarin in children are again demonstrated in this study. CONCLUSION: Further studies are warranted using other thromboprophylactic agents with less or no monitoring and fewer drug interactions, including the newer anticoagulant agents such as direct thrombin inhibitors.


Subject(s)
Anticoagulants/therapeutic use , Catheterization, Central Venous/adverse effects , Venous Thrombosis/prevention & control , Warfarin/therapeutic use , Anticoagulants/administration & dosage , Catheters, Indwelling/adverse effects , Child , Humans , Neoplasms/drug therapy , Warfarin/administration & dosage
12.
Stroke ; 37(1): 116-22, 2006 Jan.
Article in English | MEDLINE | ID: mdl-16322494

ABSTRACT

BACKGROUND AND PURPOSE: Clinical trials are lacking in pediatric stroke. As a result, physicians caring for children with stroke face significant challenges. The patient characteristics and specific nature of clinical challenges facing practicing clinicians can inform the design of and priorities for developing relevant clinical trials. METHODS: Physicians consulted the 1-800-NOCLOTS toll-free pediatric stroke telephone consultation service on children (birth to 18 years) with ischemic stroke. Pediatric neurologist or hematologists provided telephone consultation and documented caller and patient characteristics, antithrombotic treatments and callers' questions for entry into a computerized database. Children referred from January 1, 1995 to January 1, 2004, comprised the study cohort. RESULTS: Stroke consults were completed on 1065 children located predominantly in the United States (76%). Children had arterial ischemic stroke (AIS; 679; 64%) or cerebral sinovenous thrombosis (CSVT; 386; 36%) and were 54% male and 16% neonates. Risk factors and antithrombotic agents (none, aspirin, warfarin, and heparins) differed by stroke type. In 60% of patients, callers had not initiated antithrombotic therapy. Callers' questions for both stroke types usually concerned treatment selection (83%), but for AIS, questions more frequently (P<0.0001) concerned the selection and interpretation of etiological investigations. CONCLUSIONS: Research is urgently needed in pediatric stroke to provide direction for management in "real-life" settings. Research efforts should address the unique challenges within different stroke types and include observational studies addressing investigation of the child with AIS. For AIS and CSVT, randomized controlled trials investigating the efficacy of antithrombotic treatment are urgently needed.


Subject(s)
Stroke/diagnosis , Stroke/therapy , Telemedicine/methods , Adolescent , Child , Child, Preschool , Clinical Trials as Topic , Cohort Studies , Echocardiography , Female , Fibrinolytic Agents/therapeutic use , Hematology/methods , Humans , Ischemia/pathology , Male , Nervous System Diseases/pathology , Neurology/methods , Risk Factors , Stroke/pathology , Vascular Diseases/pathology , Venous Thrombosis/pathology
13.
Thromb Haemost ; 94(3): 516-21, 2005 Sep.
Article in English | MEDLINE | ID: mdl-16268465

ABSTRACT

Venous thromboembolic events (VTE) in children are frequently associated with central venous lines (CVL). Identifying risk factors related to CVL management could potentially minimize CVL-related thrombotic complications. The objectives of the study were to assess whether CVL location, type, size, and duration of placement are associated with the incidence of VTE in children. The study was a prospective, multicentre cohort study in a general pediatric population requiring CVL. Data on CVL characteristics were documented prospectively using standardized case report forms. Outcome assessments were by i) clinical monitoring for symptomatic VTE which were confirmed by appropriate objective test, or ii) screening by venography at study exit. Among 158 children, 21 (13%) hadVTE. The incidence of VTE was increased with femoral CVL (32%) and subclavian CVL (27%) compared to brachial CVL (12%) and jugular CVL (8%; p = 0.01). The incidence of VTE was independent of CVL type (peripherally inserted central catheters, untunneled CVL, tunneled exteriorized CVL, subcutaneous ports; p = 0.90), and CVL size (CVL diameter, p = 0.42; number of CVL lumen, p = 0.58). The incidence of VTE did not increase with duration of CVL placement: 0-5 days (17% VTE), 6-20 days (19%), 21-35 days (10%), and 36-50 days (11%, p = 0.68). The incidence of CVL-relatedVTE may be reduced by preferred placement of CVL in brachial or jugular veins. The choice of CVL type and size does not significantly influence the risk of VTE. Short-term CVL are associated with a similar risk of VTE as longer-term CVL.


Subject(s)
Catheterization, Central Venous/adverse effects , Venous Thrombosis/etiology , Adolescent , Age Factors , Catheterization, Central Venous/methods , Child , Child, Preschool , Female , Fibrinolytic Agents/therapeutic use , Heparin, Low-Molecular-Weight/therapeutic use , Humans , Incidence , Infant , Infant, Newborn , Male , Risk Factors , Venous Thrombosis/epidemiology , Venous Thrombosis/prevention & control
14.
Pediatr Radiol ; 35(3): 258-74, 2005 Mar.
Article in English | MEDLINE | ID: mdl-15635472

ABSTRACT

Pulmonary thromboembolism (PTE) is uncommonly diagnosed in the pediatric patient, and indeed often only discovered on autopsy. The incidence of pediatric PTE depends upon the associated underlying disease, diagnostic tests used, and index of suspicion. Multiple risk factors can be found including: peripartum asphyxia, dyspnea, haemoptysis, chest pain, dehydration, septicemia, central venous lines (CVLs), trauma, surgery, ongoing hemolysis, vascular lesions, malignancy, renal disease, foreign bodies or, uncommonly, intracranial venous sinus thrombosis, burns, or nonbacterial thrombotic endocarditis. Other types of embolism can occur uncommonly in childhood and need to be recognized, as the required treatment will vary. These include pulmonary cytolytic thrombi, foreign bodies, tumor and septic emboli, and post-traumatic fat emboli. No single noninvasive test for pulmonary embolism is both sensitive and specific. A combination of diagnostic procedures must be used to identify suspect or confirmed cases of PTE. This article reviews the risk factors, clinical presentation and treatment of pulmonary embolism in children. It also highlights the current diagnostic tools and protocols used to evaluate pulmonary embolism in pediatric patients.


Subject(s)
Diagnostic Imaging , Pulmonary Embolism/diagnosis , Child , Diagnosis, Differential , Humans , Pulmonary Embolism/etiology , Pulmonary Embolism/therapy , Risk Factors
15.
Thromb Haemost ; 92(4): 678-81, 2004 Oct.
Article in English | MEDLINE | ID: mdl-15467895

ABSTRACT

The implications of currently available data on the association of gestational vascular complications with thrombophilia are presented in this consensus report. Screening is recommended for women with the following previous complications: fetal loss including three or more first trimester loss, two or more second trimester loss, or any stillbirth; early, severe or recurrent preeclampsia and severe intrauterine growth restriction. Maternal antithrombotic therapy is currently evaluated in women with thrombophilia and previous complications.


Subject(s)
Pregnancy Complications, Hematologic/etiology , Thrombophilia/complications , Abortion, Habitual/blood , Abortion, Habitual/etiology , Adult , Contraindications , Female , Fibrinolytic Agents/therapeutic use , Humans , Practice Guidelines as Topic , Pregnancy , Pregnancy Complications, Hematologic/drug therapy , Pregnancy Outcome , Thrombophilia/diagnosis , Thrombophilia/drug therapy
16.
Thromb Haemost ; 92(4): 722-8, 2004 Oct.
Article in English | MEDLINE | ID: mdl-15467901

ABSTRACT

Thromboembolism (TE) has recently been recognized as a clinical entity in children. Determining the clinical characteristics of pediatric TE is an important first step in dealing with this new disorder. The paper summarizes 1776 consecutive children with systemic TE referred to 1-800-NO-CLOTS telephone consultation service. 1-800-NO-CLOTS is a free consultation service for clinicians managing pediatric TE. Patient information was collected immediately using standardized forms. In children with systemic TE, infants under one year of age (47%) including neonates (26%) represented the largest distinct pediatric age group. Age-related differences were seen in TE locations, associated conditions, and risk factors. However, venous TE was the most frequent manifestation (74%). Neonates and children with cardiac disorders were more likely to have an arterial TE than a venous TE Beyond the neonatal period, venous TE associated with a central line is more likely to occur than arterial TE. Children with ALL were 5.7 times more likely to have a venous TE than an arterial TE. TE were infrequent in otherwise healthy children with 90% of children having at least one risk factor. Central catheters were the single most common risk factor associated with TE, present in 2/3 of children. Ultrasound was most frequently employed for diagnosis of TE. Finally, there was marked heterogeneity in treatment of children with TE. In children, neonates form the largest single group with TE. TE usually occur only in the presence of one or more risk factors with catheters being the single most important factor.


Subject(s)
Thromboembolism/epidemiology , Adolescent , Arterial Occlusive Diseases/epidemiology , Catheterization/adverse effects , Child , Child, Preschool , Data Collection , Humans , Infant , Infant, Newborn , Logistic Models , Referral and Consultation , Risk Factors , Thromboembolism/diagnosis , Thromboembolism/drug therapy , Thromboembolism/etiology , Venous Thrombosis/epidemiology
18.
J Pediatr Hematol Oncol ; 26(5): 327-30, 2004 May.
Article in English | MEDLINE | ID: mdl-15111789

ABSTRACT

: The authors describe a 15-year-old girl presenting with a cerebral ischemic stroke as the first manifestation of catastrophic antiphospholipid antibody syndrome secondary to acute myeloid leukemia (AML). Despite treatment with anticoagulants, therapeutic plasma exchange, and chemotherapy, the patient developed multiorgan thromboses and failure, eventually culminating in death. This unusual presentation of AML has not been previously described in children. Clinical features of antiphospholipid antibody syndrome and current knowledge regarding its association with malignancies are reviewed.


Subject(s)
Antiphospholipid Syndrome/diagnosis , Antiphospholipid Syndrome/etiology , Leukemia, Myelomonocytic, Acute/diagnosis , Adolescent , Antibodies, Antiphospholipid/blood , Antiphospholipid Syndrome/complications , Catastrophic Illness , Diagnosis, Differential , Fatal Outcome , Female , Humans , Leukemia, Myelomonocytic, Acute/complications , Stroke/etiology , Thrombosis/etiology , Treatment Failure
19.
Semin Thromb Hemost ; 30 Suppl 1: 31-9, 2004 Feb.
Article in English | MEDLINE | ID: mdl-15085464

ABSTRACT

The incidence of thromboembolic events (TEs) in childhood is greatly underestimated. Two age groups account for approximately 70% of TEs in childhood: infants and teenagers. There are several predisposing risk factors for newborns such as small vessels, high hematocrit, and a unique neonatal hemostatic system. Central venous lines contribute to 80% of deep vein thrombosis in newborns. Other risk factors for all children are shock syndromes, trauma, surgery, heart and kidney disease, and acquired or hereditary thrombophilias. The best prophylaxis is to recognize, avoid, and remove risk factors if possible. This is particularly relevant in childhood, where risk factors can be found in the majority of TEs. The serious sequelae of TEs (mortality, and short- and long-term morbidity) require therapeutic intervention. Unfractionated heparin (UFH) has the following disadvantages: age-dependent unpredictable pharmacokinetics, the need for intravenous access for therapy and monitoring, delays in achieving therapeutic ranges, bleeding risk, the risk of heparin-induced thrombocytopenia, and osteoporosis with long-term use. Oral anticoagulants, in addition to some of these disadvantages, show considerable variation by diet (especially if there is a change from breast to bottle feeding), medication, and intercurrent illness. Review of case reports and cohort studies on 728 children treated with low-molecular-weight heparin (LMWH) indicate the following advantages over UFH: minimal monitoring, ease of administration (subcutaneous), and possibly equivalent efficacy and safety. Dose recommendations for pediatric patients cannot be directly extrapolated from those for adult patients. If dosages are calculated according to body weight, infants < 3 months (or < 5 kg) need approximately 50% more LMWH than older children or adults to reach prophylactic or therapeutic anti-factor Xa levels. Further studies are necessary to address the following: the importance of risk factors, the necessity of screening for hereditary thrombophilia, the efficacy and safety of treatment, and side effects and duration of treatment. Thromboembolic events (TEs) are considered to be rare in children. However, recent surveys reveal that TEs in children occur more often than suspected. The incidence is greatly underestimated because TEs are usually overlooked. Retrospective surveys in children treated for acute lymphoblastic leukemia with corticosteroids and asparaginase revealed clinically symptomatic TE in only 2 to 12% of patients. However, in prospective studies with routine imaging, the incidence was more than 20%. The objectives of this article are to update the present knowledge on TEs in children, including incidence, predominant age groups, risk factors, diagnosis, and indications for prophylaxis and therapy; and to discuss the use of low-molecular-weight heparin (LMWH) in children.


Subject(s)
Heparin, Low-Molecular-Weight/therapeutic use , Thromboembolism/drug therapy , Child , Female , Heparin, Low-Molecular-Weight/administration & dosage , Heparin, Low-Molecular-Weight/adverse effects , Humans , Practice Guidelines as Topic , Pregnancy , Thromboembolism/complications , Treatment Outcome
20.
Thromb Res ; 111(4-5): 227-33, 2003.
Article in English | MEDLINE | ID: mdl-14693168

ABSTRACT

BACKGROUND: Post-thrombotic syndrome (PTS) in adults, characterized by swelling, skin pigmentation, pain, and ulceration of the limb, is secondary to deep vein thrombosis (DVT). In contrast to the extensive documentation on PTS in adults, little is known about the risk of PTS in children. OBJECTIVE: To determine the incidence, clinical characteristics, and predictors of PTS in children. METHODS: A cross-sectional study in 153 nonselected children with objectively confirmed DVT. All children were assessed for PTS using a standardized score. As per the PTS score, severity was classified as: absent, mild, moderate, or severe. RESULTS: Post-thrombotic syndrome was present in 96/153 children (63%), in which 80 (83%) were mild and 16 (17%) were moderate. Swelling was the most frequently recorded subjective symptom (43%) while increased limb circumference (71%) and presence of collateral circulation (53%) were the most frequently recorded objective symptoms. Risk factors for development of PTS were: lack of resolution of the DVT by radiographic assessment (OR 3.96, 95% CI 1.68-9.30), number of vessels involved in the initial DVT (OR 2.05, 95% CI 1.52-2.77), and length of follow-up (OR 1.22, 95% CI 1.08-1.39). CONCLUSIONS: These findings demonstrate that PTS is a clinically significant disease in children with previous DVT.


Subject(s)
Leg Ulcer/epidemiology , Pain/epidemiology , Postphlebitic Syndrome/epidemiology , Risk Assessment/methods , Venous Insufficiency/epidemiology , Venous Thrombosis/epidemiology , Adolescent , Adult , Canada , Child , Child, Preschool , Cross-Sectional Studies , Female , Humans , Incidence , Infant , Infant, Newborn , Male , Risk Factors , Severity of Illness Index
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