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1.
Pediatr Cardiol ; 28(3): 213-20, 2007.
Article in English | MEDLINE | ID: mdl-17404682

ABSTRACT

We document the presentation profiles, treatment strategies, and clinical outcomes in a relatively large cohort of pediatric patients with intracardiac thrombi (ICT). We performed a retrospective review of patients diagnosed with ICT by echocardiography at a tertiary pediatric hospital during a 10-year period. These patients received medical therapy or thrombectomy. We provided echocardiographic descriptions of the ICT-size, chamber location, and mobility/morphology. The outcome measures were ICT (persistence, resolution, or embolization), effectiveness of therapy, and patient morbidity and mortality. There were 40 ICT diagnosed in 31 patients (22 males and 9 females). Mean age at diagnosis was 8.8 years (range, 15 days to 18 years). Overall mortality was 12/31 patients (39%); only one death was attributed to ICT embolization. Embolic events occurred in 4/31 patients (13%). The most common initial therapies included heparin infusion (n = 15), warfarin (n = 7), and aspirin (n = 7). The ICT resolved with medical therapy alone in 19/30 patients (63%). One patient required surgical thrombectomy. The cohort was divided into group 1 (dilated cardiomyopathy), group 2 (status post Fontan operation), and group 3 (other diagnoses). In group 1 (n = 11), there were 8 deaths. Embolization occurred in 2/5 large ICT, resulting in cerebral infarction and death (n = 1) and renal infarction (n = 1). The most common ICT location was the left ventricle (n = 10). Severe ventricular systolic dysfunction was present in 10/11 patients (91%). In group 2 (n = 9), there was 1 death. Embolization occurred in 1/7 large ICT, resulting in seizures and temporary paresis. All ICT were located in the Fontan pathway. Severe ventricular systolic dysfunction was present in 2/9 patients (22%). In group 3 (n = 11), there were 3 deaths. Embolization occurred in 1/9 small ICT, resulting in coronary emboli. ICT are most commonly diagnosed in pediatric patients with dilated cardiomyopathy or patients status post Fontan operation. The majority of ICT resolve with medical therapy. Larger ICT tend to embolize more frequently, and the morbidity secondary to embolization is significant. Rarely is mortality due to ICT embolization. The prognosis is poor for patients with left ventricular ICT or ICT in the presence of ventricular systolic dysfunction.


Subject(s)
Heart Diseases/diagnostic imaging , Thrombosis/diagnostic imaging , Adolescent , Cardiomyopathy, Dilated/drug therapy , Cardiomyopathy, Dilated/mortality , Child , Child, Preschool , Epidemiologic Methods , Female , Fontan Procedure/statistics & numerical data , Heart Diseases/drug therapy , Heart Diseases/mortality , Humans , Infant , Infant, Newborn , Male , Sex Distribution , Thrombosis/drug therapy , Thrombosis/mortality , Treatment Outcome , Ultrasonography
3.
J Am Coll Cardiol ; 36(7): 2279-83, 2000 Dec.
Article in English | MEDLINE | ID: mdl-11127473

ABSTRACT

OBJECTIVES: We sought to determine if early primary repair of acyanotic tetralogy of Fallot (ToF) can be performed safely with low requirement for transannular patching (TAP) and thereafter allow normal right ventricular outflow tract (RVOT) growth. BACKGROUND: Early primary repair of ToF normalizes intracardiac flow patterns, which may allow subsequent normal RVOT growth. Traditionally repair is deferred until symptoms occur or children are deemed of adequate size for operative risk to be acceptable because of a perceived increased requirement for TAP in small infants. METHODS: Between July 1992 and March 1999, 42 acyanotic infants aged 4 to 87 days (median 62) and weight 2.6 to 6.6 kg (median 4.55) underwent complete repair of ToF. Pulmonary annulus measured 4 to 10.5 mm (median 6.5) with "z-value" of-5.6 to +3.0 (median -1.9). RVOT reconstruction was tailored to each patient; pulmonary valvotomy was performed in 26, main pulmonary arterioplasty in 22, and infundibular patching in 2. Only 10 (24%) required TAP. RESULTS: Postoperative RVOT gradient was 0 to 30 mm Hg (median 10) and pRV/pLV ratio 0.3 to 0.6 (median 0.44). Pulmonary insufficiency was trivial/mild. There were no deaths. Junctional ectopic tachycardia developed in seven; only one required treatment. ICU stay was 2 to 14 days (median 4) and hospital stay 4 to 22 days (median 7). At follow-up 12 to 64 months later (median 38) there were no deaths. One child required reoperation for recurrent RVOT obstruction and two required balloon pulmonary arterioplasty. Follow-up RVOT gradient was 0 to 36 mm Hg (median 12), unchanged from early postoperative condition, and median z-value was -1.2 (-2.8 to +2.5); pulmonary insufficiency remained trivial/mild. CONCLUSIONS: Complete repair of acyanotic ToF can be performed in early infancy with low morbidity and mortality and low requirement for TAP. Though results are not statistically significant, early repair may allow normal RVOT growth thereafter.


Subject(s)
Tetralogy of Fallot/surgery , Coronary Circulation , Elective Surgical Procedures , Humans , Infant , Infant, Newborn , Morbidity , Pulmonary Valve , Retrospective Studies , Tetralogy of Fallot/physiopathology , Treatment Outcome
4.
Pediatr Cardiol ; 21(3): 253-8, 2000.
Article in English | MEDLINE | ID: mdl-10818186

ABSTRACT

Congenital coronary arterial fistulas are rare anomalies that have traditionally been managed by surgical ligation. However, in recent years endovascular therapy has been employed with encouraging results. Between 1993 and 1996, we performed transcatheter coil embolization of coronary arterial fistulas to the right atrium or ventricle in four children ranging in age from 4.5 to 9.8 years. Cardiac and coronary arterial anatomy were diagnosed correctly on the preoperative echocardiogram in all patients, including the origin, course, and termination of the fistulas. The fistula was occluded completely in three of the patients, whereas trivial residual flow remained in the fourth. Transesophageal echocardiography was useful for monitoring the embolization procedure. In one of the patients, the fistula reopened while the child was on overnight heparin, although the magnitude of flow was less than that before the embolization. At follow-up ranging from 10 to 43 months, there was no flow through the fistula in any patient. We present our experience with these patients, with a focus on the importance of echocardiographic evaluation before, during, and after transcatheter therapy of coronary arterial fistulas.


Subject(s)
Coronary Vessel Anomalies/therapy , Embolization, Therapeutic , Fistula/therapy , Child , Child, Preschool , Coronary Vessel Anomalies/diagnostic imaging , Echocardiography, Doppler, Color , Echocardiography, Transesophageal , Fistula/diagnostic imaging , Humans
5.
Appl Opt ; 15(7): 1679-80, 1976 Jul 01.
Article in English | MEDLINE | ID: mdl-20165244
6.
Appl Opt ; 14(11): 2614-21, 1975 Nov 01.
Article in English | MEDLINE | ID: mdl-20155074

ABSTRACT

Image transfer properties of interferometrically produced dielectric light guides are investigated. A general technique of analysis is developed. Computer calculations based on this approach are used to study the behavior of pulses traversing the guiding structures for various values of refractive index. Experimental results are obtained using photosensitized polymethyl methacrylate as the recording material. Computer results are compared with existing theory and found to be in close agreement.

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