Successful Use of Argatroban in Pediatric Patients Requiring Anticoagulant Alternatives to Heparin.

Blood ◽  
2004 ◽  
Vol 104 (11) ◽  
pp. 4085-4085 ◽  
Author(s):  
Wendy Y. Tcheng ◽  
Wing-Yen Wong

Abstract BACKGROUND: Heparin-induced thrombocytopenia (HIT) is a potentially devastating immune-mediated complication that occurs in 1-2% of heparin-exposed pediatric patients in the ICU. Thrombosis can occur 5-14 days following heparin initiation and may cause significant morbidity and mortality. The thrombotic risk of HIT is mediated by heparin-platelet factor 4 antibody complexes that trigger platelet and endothelium activation, resulting in increased thrombin production. Argatroban is a direct thrombin inhibitor that is currently approved for use in adults for the prophylaxis or treatment of HIT. There is limited argatroban experience in the pediatric population. METHODS: A retrospective review of all pediatric patients (age < 18 years) who received argatroban at our institutions (1,2) was performed. Data collected: age, diagnosis, indication for argatroban use, dose, duration, concurrent medications, measures of coagulation, adverse effects, and outcome. RESULTS: Six pediatric patients who received argatroban anticoagulation were identified (Table 1). Ages ranged from 8 months to 16 years. Indications included HIT or history of HIT on ECMO, HIT with thrombosis, and refractory thrombosis unrelated to HIT. Argatroban was infused at a dosing range of 0.5 to 24 mcg/kg/min with goal PTT at 2X baseline. Duration of therapy ranged from 1–39 days. All cases were successfully anticoagulated on argatroban. Termination of therapy occurred when ECMO was discontinued (cases 1, 2, 4), when HIT was ruled out (case 3), when patient was converted to coumadin (case 5), and at the time of surgery (case 6). There were no significant thrombotic nor bleeding episodes during argatroban therapy. CONCLUSIONS: Our limited experience demonstrates that Argatroban can be an effective means of anticoagulation in pediatric patients who require alternatives to heparin therapy. An ongoing multi-center study to evaluate the safety and efficacy of argatroban in the pediatric population will help to determine appropriate pediatric dosing. Table 1. Argatroban in Pediatrics Case Age/Gender Diagnosis Indication for Argatroban Initial Dose (μ g/kg/min) Dosing Range (μg/kg/min) Therapy Duration (days) Complications ECMO= extracorporeal membrane oxygenation, HPF4= Heparin-Platelet Factor 4, OHT= orthotopic heart transplant, WPW= Wolf-Parkinson-White syndrome, RLE= right lower extremity, DVT= deep vein thrombosis, B-T= Blalock-Taussig. 1 8 yo M Dilated cardiomyopathy, requiring ECMO Thrombus in circuit on day 4 of ECMO, +HPF4 ELISA 0.5 0.5 to 1.5, stabilized at 1.0 6 None 2 16 yo M Complex congenital heart disease, idiopathic cardiomyopathy s/p OHT, acute rejection requiring ECMO History of +HPF4 ELISA 2.0 0.6–2.0, stabilized at 0.6–0.8 10 None 3 8 yo F Complex congenital heart disease, heart failure requiring ECMO Concern for HIT when initiating ECMO, HPF4 ELISA pending 2.0 1.5–2.0 1 None 4 15 mo F Dilated cardiomyopathy,heart failure requiring ECMO Dropping platelets, and +HPF4 ELISA on day #10 ECMO 2.0 2.0–3.5 during 1st week, rate increased to 24 during 2nd week, then stabilized at 13–15 39 None 5 16 yo F History of right femoral osteosarcoma and WPW requiring ablation by cardiac catheterization RLE DVT after cardiac catheterization; DVT refractory to heparin & thrombolytic therapy 2.0 2.0 10 None 6 8 mo F Complex congenital heart disease Thrombosed B-T shunt, +HPF4 ELISA 1.0 0.5–1.0 9 None

2013 ◽  
Vol 53 (3) ◽  
pp. 173
Author(s):  
Sri Endah Rahayuningsih

Background Congenital heart disease (CHD) may occur inseveral members of a family. Studies have shown that familialgenetic factor play a role in CHD.Objective To identify familial recurrences of CHD in familieswith at least one member treated for CHD in Dr. Hasan SadikinHospital, Bandung Indonesia.Methods In this descriptive study, subjects were CHD patientshospitalized or treated from January 2005 to December 2011. Weconstructed family pedigrees for five families.Results During the study period, there were 1,779 patients withCHD. We found 5 families with 12 familial CHD cases, consistingof 8 boys and 4 girls. Defects observed in these 12 patients weretetralogy of Fallot, transposition of the great arteries, persistentductus arteriosus, ventricular septa! defect, tricuspid atresia,pulmonary stenos is, and dilated cardiomyopathy. Persistent ductusarteriosus was the most frequently observed defect (4 out of 12subjects) . None of the families had a history of consanguinity. Therecurrence risk of CHD among siblings was calculated to be 0.67%,and the recurrence risk ofCHD among cousins was 0.16%.Conclusion Familial CHD may indicate the need for geneticcounseling and further pedigree analysis.


PEDIATRICS ◽  
1968 ◽  
Vol 41 (1) ◽  
pp. 123-129
Author(s):  
Blanche P. Alter ◽  
Emily E. Czapek ◽  
Richard D. Rowe

Sweating was found to be increased in children with congenital heart disease who had a propensity to congestive heart failure, e.g., children with endocardial fibroelastosis or large or moderate sized left-to-right shunts. This was suggested in a review of cardiac clinic records of 220 patients and was supported by the results of pilocarpine sweat tests which were performed on 34 cardiac patients. By history and by measurement of the amount of sweat produced, children with a history of or tendency toward heart failure could be predicted though patients did not need to be in failure when tested. Contrary to previous opinion, the left-to-right shunt was not in itself sufficient to cause the child to sweat. The shunt had to be large enough to be associated with failure at some time. It is suggested that the pilocarpine sweat test might actually be useful as an aid in predicting a child's potential for heart failure. Several theories regarding the mechanism of sweating in these situations are discussed.


2020 ◽  
Vol 300 ◽  
pp. 137-140 ◽  
Author(s):  
Susanne J. Maurer ◽  
Claudia Pujol Salvador ◽  
Sandra Schiele ◽  
Alfred Hager ◽  
Peter Ewert ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-12 ◽  
Author(s):  
Christine H. Attenhofer Jost ◽  
Dörthe Schmidt ◽  
Michael Huebler ◽  
Christian Balmer ◽  
Georg Noll ◽  
...  

Due to impressive improvements in surgical repair options, even patients with complex congenital heart disease (CHD) may survive into adulthood and have a high risk of end-stage heart failure. Thus, the number of patients with CHD needing heart transplantation (HTx) has been increasing in the last decades. This paper summarizes the changing etiology of causes of death in heart failure in CHD. The main reasons, contraindications, and risks of heart transplantation in CHD are discussed and underlined with three case vignettes. Compared to HTx in acquired heart disease, HTx in CHD has an increased risk of perioperative death and rejection. However, outcome of HTx for complex CHD has improved over the past 20 years. Additionally, mechanical support options might decrease the waiting list mortality in the future. The number of patients needing heart-lung transplantation (especially for Eisenmenger’s syndrome) has decreased in the last years. Lung transplantation with intracardiac repair of a cardiac defect is another possibility especially for patients with interatrial shunts. Overall, HTx will remain an important treatment option for CHD in the near future.


Circulation ◽  
2014 ◽  
Vol 130 (suppl_2) ◽  
Author(s):  
Robert M Hayward ◽  
Elyse Foster ◽  
Zian H Tseng

Background: Labor, delivery, and the postpartum period are a time of increased arrhythmia and congestive heart failure (CHF) incidence. With improvements in the treatment of congenital heart disease (CHD), more women are reaching childbearing age and may be at increased risk for cardiac events and mortality during pregnancy and delivery. Methods: The Healthcare Cost and Utilization Project was used to identify admissions for vaginal and cesarean delivery in California hospitals between 1/1/2005 and 12/31/2011. We compared length of stay, in-hospital mortality, incident CHF, cardiac arrest, and incident arrhythmias for women without CHD to women with non-complex CHD (NC-CHD) and complex CHD (C-CHD). Results: We identified 2,720,980 deliveries resulting in 2,770,382 live births (74% of live births in the state over this period), which included 3,218 women with NC-CHD and 248 women with C-CHD. History of CHF was more common in women with CHD (8.1% for C-CHD, 2.6% for NC-CHD, and 0.08% for women without CHD, p<0.00005 for NC-CHD compared to no CHD and for C-CHD compared to no CHD). Those with CHD were more likely to undergo cesarean section (Table 1). Length of stay was significantly longer in women with CHD (2.6 ± 2.3 days for women without CHD, 3.4 ± 10.2 days for women with NC-CHD and 5.0 ± 13.3 days for women with C-CHD). In-hospital mortality was not significantly higher in women with CHD (Table 1). Incident heart failure, arrhythmias, and cardiac arrest were uncommon in all groups (Table 1). Conclusions: In this study of 2.7 million women admitted to California hospitals for delivery, women with CHD were more likely to undergo cesarean section and had longer length of stay. Despite more frequent history of CHF in women with CHD, incident CHF and arrhythmias were rare during hospitalization. In-hospital mortality and cardiac arrest were not higher in CHD patients. These results suggest that in pregnant women with CHD, cardiac events and mortality at the time delivery are uncommon.


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