Progressive congenital valvar aortic stenosis during infancy: five cases.

abstract：:Venous correction for complete transposition with intact ventricular septum remains the preferred surgical option in most centers (Mustard or Senning procedures). The long-term function of the morphologically right ventricle and tricuspid valve, which continue to sustain the systemic circulation thereafter, remains a ...

journal_title：Pediatric cardiology

authors： Smith A,Wilkinson JL,Anderson RH,Arnold R,Dickinson DF

更新日期：1986-01-01 00:00:00

abstract：:The objective of this investigation was to compare how two modes of positive pressure ventilation affect cardiac output, airway pressures, oxygenation, and carbon dioxide removal in children with congenital heart disease in the immediate postoperative period. The investigation used a one group pretest-post-test study ...

journal_title：Pediatric cardiology

authors： Kocis KC,Dekeon MK,Rosen HK,Bandy KP,Crowley DC,Bove EL,Kulik T

更新日期：2001-05-01 00:00:00

abstract：:In a patient with single ventricle, mitral atresia, common atrium, pulmonary stenosis, azygos continuation of the inferior vena cava and bilateral systemic artery--pulmonary artery anastomoses, the systemic veins were connected directly to the pulmonary arteries to achieve physiologic repair; the child was discharged ...

journal_title：Pediatric cardiology

authors： Waldman JD,Lamberti JJ

更新日期：1986-01-01 00:00:00

abstract：:A blood pump specifically designed to augment flow from the great veins through the lungs would ameliorate the poor physiology of the failing univentricular circulation and result in a paradigm shift in the treatment strategy for Fontan patients. This study is the first to examine mechanical cavopulmonary assistance w...

journal_title：Pediatric cardiology

authors： Throckmorton AL,Lopez-Isaza S,Downs EA,Chopski SG,Gangemi JJ,Moskowitz W

更新日期：2013-08-01 00:00:00

abstract：:Coronary artery fistula (CAF) is a rare congenital anomaly that can be complicated by endocarditis, myocardial infarction, or coronary aneurysms. This article reviews the clinical characteristics and surgical outcome of 10 patients with CAF in Rajae Heart Center. From 1990 to 2000, 10 patients (age, 6 months to 15 yea...

journal_title：Pediatric cardiology

authors： Malekahmadi M,Shahmohammadi A

更新日期：2005-07-01 00:00:00

abstract：:Presented is a retrospective outcome study of a 15-year single institutional experience with a contemporary cohort of patients with hypoplastic left heart syndrome and complex that underwent a "Giessen Hybrid" stage I as initial palliation. Hybrid approach consisting of surgical bilateral pulmonary artery banding and ...

journal_title：Pediatric cardiology

authors： Schranz D,Bauer A,Reich B,Steinbrenner B,Recla S,Schmidt D,Apitz C,Thul J,Valeske K,Bauer J,Müller M,Jux C,Michel-Behnke I,Akintürk H

更新日期：2015-02-01 00:00:00

abstract：:In our institute, 1100 patients with a history of Kawasaki disease have been catheterized for selective coronary arteriography. Their age at examination ranged from four months to 13 years. Coronary artery lesions (CAL) were found in 262 patients. As far as the type of the CAL was concerned, occlusion was noted in 20 ...

journal_title：Pediatric cardiology

authors： Suzuki A,Kamiya T,Kuwahara N,Ono Y,Kohata T,Takahashi O,Kimura K,Takamiya M

更新日期：1986-01-01 00:00:00

abstract：:Various agents have been suggested as causal or associated factors in the pathogenesis of Kawasaki disease (KD); however, the underlying factors of KD remain unknown. Plasma exchange is one of the most effective treatments for the acute phase of KD. This indicates that plasma may contain factors associated with the pa...

journal_title：Pediatric cardiology

authors： Kanai T,Shiraishi H,Uehara R,Ito T,Momoi MY

更新日期：2012-12-01 00:00:00

abstract：:Kawasaki disease (KD) is a self-limiting systemic vasculitis of unknown etiology. KD is often complicated by coronary artery aneurysms (CAAs), which develop in about 20-25% of untreated children and 3-5% of children treated with intravenous immunoglobulin therapy. To identify the risk loci for CAA susceptibility in pa...

journal_title：Pediatric cardiology

authors： Kwon YC,Kim JJ,Yu JJ,Yun SW,Yoon KL,Lee KY,Kil HR,Kim GB,Han MK,Song MS,Lee HD,Ha KS,Sohn S,Hong YM,Jang GY,Lee JK,Korean Kawasaki Disease Genetics Consortium.

更新日期：2019-03-01 00:00:00

abstract：:Aortic atresia and interrupted aortic arch is a rare cardiac combination. Review of the literature revealed nine cases. We present two patients with this combination and the additional finding of quadricuspid pulmonary valves, one of which was severely stenotic. In the latter patient, an aortopulmonary window was pres...

journal_title：Pediatric cardiology

authors： Yew G,Coleman D,Calder L

更新日期：2005-07-01 00:00:00

abstract：:Cardiac involvement of Duchenne and Becker muscular dystrophies (DMD/BMD) is the most common cause of fatal outcomes. It is still unclear whether some DMD/BMD gene mutations might be predictive of cardiac involvement. In this study, we provide a comprehensive overview on genotypes of cardiac disease in DMD/BMD. We sys...

journal_title：Pediatric cardiology

authors： Zhou H,Fu M,Mao B,Yuan L

更新日期：2020-10-09 00:00:00

abstract：:Serum troponin (Tn) is often elevated in viral myocarditis; however, its prognostic significance is unknown. We tested the hypothesis that abnormal serum Tn is associated with mortality in children hospitalized with myocarditis. We retrospectively studied data from six large children's hospitals participating in the P...

journal_title：Pediatric cardiology

authors： Butto A,Rossano JW,Nandi D,Ravishankar C,Lin KY,O'Connor MJ,Shaddy RE,Shamszad P

更新日期：2018-08-01 00:00:00

abstract：:A premature child with congenital complete heart block had an epicardial single-chamber pacemaker implanted at 2 days of age. At 21 months of age, while sitting or standing, the patient's right anterior thigh muscles contracted at her pulse rate. Surgical exploration revealed a free-floating pacemaker in her peritoneu...

journal_title：Pediatric cardiology

authors： Salim MA,DiSessa TG,Watson DC

更新日期：1999-03-01 00:00:00

abstract：:Currently, it is clear that primary hypertension begins in childhood and that it contributes to the early development of chronic kidney disease (CKD). Hypertension also increases the risk of cardiovascular morbidity and mortality, and that risk rises as blood pressure levels escalate. As among adult patients, overweig...

journal_title：Pediatric cardiology

authors： Assadi F

更新日期：2012-10-01 00:00:00

abstract：:To determine the influence of heart rate (HR) on systolic time intervals (STI) in neonates, serial measurements of right ventricular (RVSTI) and left ventricular systolic time intervals (LVSTI) were made on 30 healthy term newborn infants at age 4-8 h, 24-30 h, eight days, and four weeks. STI was related to HR and age...

journal_title：Pediatric cardiology

authors： Lindner W,Döhlemann C,Schneider K,Versmold H

更新日期：1985-01-01 00:00:00

abstract：:In August 2010, the Nit-Occlud® Lê (EUREVECO) became available for transcatheter coil occlusion of ventricular septal defects (VSDs). Retrospective European Registry for VSD Closure using the Nit-Occlud® Lê-VSD-Coil; analysis of the feasibility, results, safety and follow-up of VSD-closure over a 3-year period in 18 E...

journal_title：Pediatric cardiology

authors： Haas NA,Kock L,Bertram H,Boekenkamp R,De Wolf D,Ditkivskyy I,Freund MW,Gewillig M,Happel CM,Herberg U,Karthasyan E,Kozlik-Feldmann R,Kretschmar O,Kuzmenko Y,Milanesi O,Mueller G,Pongiglione G,Schubert S,Tarusinov G,

更新日期：2017-02-01 00:00:00

abstract：:Little has been published about specific problems that may occur during long-distance transports of newborn cardiac patients. During a 4-year period after centralization of pediatric heart surgery in Sweden, 286 transports were prospectively investigated. A majority (77.3%) of the transports were carried out by nonspe...

journal_title：Pediatric cardiology

authors： Hellström-Westas L,Hanséus K,Jögi P,Lundström NR,Svenningsen N

更新日期：2001-09-01 00:00:00

abstract：:Intramural coronary artery is known to be a risk factor for early death after an arterial switch operation (ASO). We evaluated the early and mid-term results of ASO for patients with intramural coronary artery. From September 2008 to March 2012, seven patients with an intramural coronary artery underwent ASO at our ho...

journal_title：Pediatric cardiology

authors： Chen X,Cui H,Chen W,Yang S,Cui Y,Xia Y,Ma L

更新日期：2015-01-01 00:00:00

abstract：:Three infants, each with a clinical picture of dilated cardiomyopathy, underwent endomyocardial biopsy. Immunohistologic analysis revealed chronic myocarditis. In one infant, a postviral etiology of chronic myocarditis could be assessed on the basis of molecular techniques. Therapy with azathioprine and prednisone res...

journal_title：Pediatric cardiology

authors： Schmaltz AA,Demel KP,Kallenberg R,Neudorf U,Kandolf R,Klingel K,Bültmann B

更新日期：1998-05-01 00:00:00

abstract：:Little data are published about right ventricular (RV) growth and function in infants and neonates after balloon pulmonary valvuloplasty (BPV) for critical valvular pulmonary stenosis (PS). We aimed to assess the RV growth and function during 1 year after BPV for critical valvular PS in neonates and infants. A total o...

journal_title：Pediatric cardiology

authors： Agha H,El-Saeidi S,Abou Seif H,Abd El-Salam M,El Amrousy D

更新日期：2020-04-01 00:00:00

abstract：:As a transcription factor mainly expressed in cardiovascular system, T-box 20 (TBX20) plays an important role in embryonic cardiovascular system development and adult heart function. Previous studies have identified associations of two SNPs in the T-box DNA-binding domain of TBX20 with congenital heart disease (CHD) i...

journal_title：Pediatric cardiology

authors： Chen J,Sun F,Fu J,Zhang H

更新日期：2015-04-01 00:00:00

abstract：:The hospitalization of a child for cardiac surgery is known to be a stressful experience for parents. However, little is known about the time course or the relationships between parental stress and the child's actual or perceived recovery. This research aimed to investigate pre- and postoperative parental stress and t...

journal_title：Pediatric cardiology

authors： Franck LS,McQuillan A,Wray J,Grocott MP,Goldman A

更新日期：2010-10-01 00:00:00

abstract：:A two-year-old child who had had palliative surgery as a neonate for an absent right atrioventricular connection and double-inlet ventricle was shown to be developmentally retarded. Trisomy for the short arm of chromosome 8 was demonstrated, resulting from a familial 8:13 translocation, with a high risk of recurrence....

journal_title：Pediatric cardiology

authors： Burn J,Baraitser M,Hughes DT,Saldana-Garcia P,Taylor JF

更新日期：1984-01-01 00:00:00

abstract：:Ionizing radiation exposure is a necessary risk entailed during congenital cardiac catheterizations. The congenital catheterization lab at Yale New Haven Children's Hospital employed quality improvement strategies to minimize radiation exposure in this vulnerable population. In two phases, we implemented six intervent...

journal_title：Pediatric cardiology

authors： Patel C,Grossman M,Shabanova V,Asnes J

更新日期：2019-03-01 00:00:00

abstract：:In the very young child (less than eight years of age), transient loss of consciousness represents a diagnostic and management dilemma for clinicians. While most commonly benign, syncope may be due to cardiac dysfunction which can be life-threatening. It can be secondary to an underlying ion channelopathy, cardiac inf...

journal_title：Pediatric cardiology

authors： Villafane J,Miller JR,Glickstein J,Johnson JN,Wagner J,Snyder CS,Filina T,Pomeroy SL,Sexson-Tejtel SK,Haxel C,Gottlieb J,Eghtesady P,Chowdhury D

更新日期：2021-01-02 00:00:00

abstract：OBJECTIVE:Heterotaxy syndrome is associated with complex cardiac malformations and cardiac conduction system abnormalities. Those with right atrial isomerism (RAI) have dual sinus nodes and dual atrioventricular nodes predisposing them to supraventricular tachycardia (SVT). Those with left atrial isomerism (LAI) lack a...

journal_title：Pediatric cardiology

authors： Ozawa Y,Asakai H,Shiraga K,Shindo T,Hirata Y,Hirata Y,Inuzuka R

更新日期：2019-06-01 00:00:00

abstract：:We sought to document morbidities and growth for patients with hypoplastic left heart syndrome (HLHS) to inform the initial surgical decision and understand healthcare needs. Data were obtained on 137 patients with HLHS, born between 1989 and 1994, who survived staged surgery ( n = 62) or transplantation ( n = 75) and...

journal_title：Pediatric cardiology

authors： Jenkins PC,Flanagan MF,Jenkins KJ,Sargent JD,Canter CE,Chinnock RE,Vincent RN,O'Connor GT

更新日期：2004-01-01 00:00:00

abstract：BACKGROUND:This study aimed to provide descriptive information about off-label treatment practice with clopidogrel in a pediatric population. METHODS:Patients less than 18 years of age prescribed clopidogrel between March 2002 and August 2005 were retrospectively identified at Children's Hospital, Boston. Data from th...

journal_title：Pediatric cardiology

authors： Maltz LA,Gauvreau K,Connor JA,Jenkins KJ

更新日期：2009-02-01 00:00:00

abstract：:In chronic aortic insufficiency (AI), left-ventricular (LV) dysfunction must be detected early to allow timely surgery. Strain and strain rate have been used for this purpose in adults, but the value of this method in pediatric AI has not been established. Forty patients with moderate to severe AI were included in thi...

journal_title：Pediatric cardiology

authors： Lowenthal A,Tacy TA,Behzadian F,Punn R

更新日期：2013-08-01 00:00:00

abstract：:Cardiac rhabdomyoma (CR) is the most common cardiac tumor in newborns. Approximately 75% of cases are associated with tuberous sclerosis complex. Although these tumors usually spontaneously regress after 2 years of age, they can be life-threatening when they obstruct major cardiac inflow or outflow pathways. Everolimu...

journal_title：Pediatric cardiology

authors： Chang JS,Chiou PY,Yao SH,Chou IC,Lin CY

更新日期：2017-10-01 00:00:00