Latent rheumatic heart disease: outcomes 2 years after echocardiographic detection.

Abstract:

:Screening with portable echocardiography has uncovered a large burden of latent rheumatic heart disease (RHD) among asymptomatic children in endemic regions, the significance of which remains unclear. This study aimed to determine the 2-year outcomes for children with latent RHD diagnosed by echocardiographic screening. Children identified with latent RHD enrolled in a biannual follow-up program. Risk factors for disease persistence and progression were examined. Of 62 children, 51 (82 %) with latent RHD had a median follow-up period of 25 months. Of these 51 children, 17 (33.3 %) reported an interval sore throat or symptoms consistent with acute rheumatic fever (ARF). Of 43 children initially classified as having borderline RHD, 21 (49 %) remained stable, 18 (42 %) improved (to no RHD) and 4 (10 %) worsened to definite RHD. Of the 8 children initially classified as having definite RHD, 6 (75 %) remained stable, and 2 (25 %) improved to borderline RHD. Two children had confirmed episodes of recurrent ARF, one of which represented the sole case of clinical worsening. The risk factors for disease persistence or progression included younger age (p = 0.05), higher antistreptolysin O titers at diagnosis (p = 0.05), and more morphologic valve abnormalities (p = 0.01). After 2 years, most of the children had a benign course, with 91 % remaining stable or showing improvement. Education may improve recognition of streptococcal sore throat. Longer-term follow-up evaluation, however, is warranted to confirm disease progression and risk factor profile. This could help tailor screening protocols for those at highest risk.

journal_name

Pediatr Cardiol

journal_title

Pediatric cardiology

authors

Beaton A,Okello E,Aliku T,Lubega S,Lwabi P,Mondo C,McCarter R,Sable C

doi

10.1007/s00246-014-0925-3

subject

Has Abstract

pub_date

2014-10-01 00:00:00

pages

1259-67

issue

7

eissn

0172-0643

issn

1432-1971

journal_volume

35

pub_type

杂志文章
  • Interventional VSD-Closure with the Nit-Occlud® Lê VSD-Coil in 110 Patients: Early and Midterm Results of the EUREVECO-Registry.

    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

    pub_type: 杂志文章,多中心研究

    doi:10.1007/s00246-016-1502-8

    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

  • The role of transesophageal echocardiography during surgery for patients with tetralogy of Fallot.

    abstract::Routine use of intraoperative transesophageal echocardiography (TEE) is a safe monitoring and diagnostic method during pediatric congenital cardiac surgery. However, the question of whether intraoperative TEE is accurate and cost effective for patients with tetralogy of Fallot (TOF) has not been raised. This study aim...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0423-4

    authors: Kim SJ,Park SA,Song J,Shim WS,Choi EY,Lee SY

    更新日期:2013-02-01 00:00:00

  • Long-distance transports of newborn infants with congenital heart disease.

    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

    pub_type: 杂志文章

    doi:10.1007/s002460010254

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

    更新日期:2001-09-01 00:00:00

  • Decision-Making in the Catheter Laboratory: The Most Important Variable in Successful Outcomes.

    abstract::Increasingly the importance of how and why we make decisions in the medical arena has been questioned. Traditionally the aeronautical and business worlds have shed a light on this complex area of human decision-making. In this review we reflect on what we already know about the complexity of decision-making in additio...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章,评审

    doi:10.1007/s00246-020-02295-1

    authors: Duignan S,Walsh KP,McMahon CJ

    更新日期:2020-03-01 00:00:00

  • Hemolytic anemia secondary to modified blalock-taussig shunt.

    abstract::The Norwood procedure with a modified Blalock-Taussig shunt (MBTS) is the first of the three-stage surgical palliation for infants with hypoplastic left heart syndrome. We report a patient with schistocytic hemolytic anemia that developed following a right MBTS with a Gore-Tex graft. Hemolysis associated with a MBTS h...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-006-1410-4

    authors: Ryerson LM,Wechsler SB,Ohye RG

    更新日期:2007-05-01 00:00:00

  • Risk factors for interstage death after the Norwood procedure.

    abstract::Operative survival after the Norwood procedure has significantly improved during the past 10 years. However, there remains attrition among Norwood survivors before reaching planned second-stage palliation. The purpose of this study was to evaluate potential risk factors for interstage mortality among Norwood survivors...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-004-0776-4

    authors: Simsic JM,Bradley SM,Stroud MR,Atz AM

    更新日期:2005-07-01 00:00:00

  • Prenatal diagnosis of congenital heart disease and birth outcomes.

    abstract::This study was undertaken to examine the impact that prenatal diagnosis of congenital heart disease (CHD) has on birth and early neonatal outcomes. The prevalence of prenatally diagnosed CHD has risen over the past decade, but the effect that prenatal diagnosis of CHD has on peripartum decisions remains unclear. No co...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0504-4

    authors: Landis BJ,Levey A,Levasseur SM,Glickstein JS,Kleinman CS,Simpson LL,Williams IA

    更新日期:2013-03-01 00:00:00

  • Effect of ventriculotomy on right-ventricular remodeling in hypoplastic left heart syndrome: a histopathological and echocardiography correlation study.

    abstract::The objective of this study was to compare histopathological changes in hypoplastic left heart syndrome right ventricles (RV) of patients undergoing Sano and modified Blalock-Taussig (MBT) shunt and correlate them with echocardiographic findings. Myocardial tissue samples were obtained from hearts with Sano or MBT shu...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0462-x

    authors: Menon SC,Erickson LK,McFadden M,Miller DV

    更新日期:2013-02-01 00:00:00

  • Architecture of the ventricular mass and atrioventricular valves in complete transposition with intact septum compared with the normal: I. The left ventricle, mitral valve, and interventricular septum.

    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

    pub_type: 杂志文章

    doi:

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

    更新日期:1986-01-01 00:00:00

  • Congenital malformations of the tricuspid valve in siblings.

    abstract::The occurrence of familial heart disease in association with tricuspid atresia is rare. The first reported instance of tricuspid atresia and Ebstein's anomaly in siblings is presented. The presence of these two distinct pathologic variants of tricuspid valve malformations in siblings suggests that these malformations ...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s002469900072

    authors: Grant JW

    更新日期:1996-09-01 00:00:00

  • Prevalence of obesity among patients with congenital and acquired heart disease.

    abstract::Overweight and obesity rates have risen dramatically in the United States, with subsequent detrimental comorbidity risks. The rates for obesity among children with congenital and acquired heart disease have rarely been reported. A retrospective cross-sectional study was conducted to determine the prevalence of overwei...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-011-0049-y

    authors: Shustak RJ,McGuire SB,October TW,Phoon CK,Chun AJ

    更新日期:2012-01-01 00:00:00

  • Predictive value of myocardial delayed enhancement in Duchenne muscular dystrophy.

    abstract::In other cardiomyopathies, cardiac magnetic resonance imaging (CMR)-derived myocardial delayed enhancement (MDE), a marker of myocardial fibrosis, is a risk factor for sudden cardiac death (SCD). In Duchenne muscular dystrophy (DMD), the prognostic value of MDE for ventricular arrhythmias and death is unknown. This st...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-014-0929-z

    authors: Menon SC,Etheridge SP,Liesemer KN,Williams RV,Bardsley T,Heywood MC,Puchalski MD

    更新日期:2014-10-01 00:00:00

  • Isolated left-sided scimitar vein connecting all left pulmonary veins to the right inferior vena cava.

    abstract::When the common pulmonary vein fails to develop, the embryonic connections of the pulmonary veins to one or more of the systemic veins almost always persist. Anomalous pulmonary venous connections to the inferior vena cava (IVC) are typically characterized by hypoplasia of the involved pulmonary veins and pulmonary ar...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-005-0920-9

    authors: Juraszek AL,Cohn H,Van Praagh R,Van Praagh S

    更新日期:2005-11-01 00:00:00

  • Warfarin anticoagulation after congenital heart surgery at a large children's hospital.

    abstract::Management of warfarin in pediatric patients remains a clinical challenge. Warfarin may be administered after congenital heart surgery, and the risks of morbidity can be high. Currently, no data exist to describe the initiation of warfarin and the risk factors for morbidity in post-congenital heart surgery patients. T...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0351-3

    authors: Lowry AW,Moffett BS,Moodie D,Knudson JD

    更新日期:2012-12-01 00:00:00

  • The wandering pacemaker: intraperitoneal migration of an epicardially placed pacemaker and femoral nerve stimulation.

    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

    pub_type: 杂志文章

    doi:10.1007/s002469900430

    authors: Salim MA,DiSessa TG,Watson DC

    更新日期:1999-03-01 00:00:00

  • Prolonged supine hypertension due to midodrine use in an orthostatic hypotensive child.

    abstract::Midodrine hydrochloride is a potent peripherally-acting alpha1 agonist that is well absorbed and rapidly metabolized to its active metabolite. It has been used for the treatment of refractory syncope but has the important side effect of supine hypertension. A 10-year-old boy with severe symptomatic orthostatic hypoten...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-006-0169-y

    authors: Olgar S,Omeroglu RE

    更新日期:2007-07-01 00:00:00

  • Anterosuperior diverticula of the right ventricle: morphological spectrum and long-term outcome of a distinct cardiac anomaly.

    abstract::Right-ventricular diverticula (RVD), although rare, have particular characteristics. Our study describes the morphology of anterosuperior diverticula of the right ventricle (RV) and patient outcome for this anomaly. Retrospective analysis was performed on all patients with anterosuperior RVD diagnosed in two tertiary ...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-014-0885-7

    authors: Wiegand G,Rauch R,Singer H,Koch A,Hofbeck M

    更新日期:2014-08-01 00:00:00

  • Correction to: Routine Sildenafil Does Not Improve Clinical Outcomes After Fontan Operation.

    abstract::The original version of this article unfortunately contained a mistake. The presentation of Table 2 was incorrect .The corrected table is given below. ...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章,已发布勘误

    doi:10.1007/s00246-018-1816-9

    authors: Collins JLG,Law MA,Borasino S,Erwin WC,Cleveland DC,Alten JA

    更新日期:2018-03-01 00:00:00

  • Correction to: Blalock-Taussig Shunt Size: Should it be Based on Body Weight or Target Branch Pulmonary Artery Size?

    abstract::The original version of the article unfortunately contained an alignment error in Table 1. The correct version of Table 1 is given below. ...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章,已发布勘误

    doi:10.1007/s00246-018-1978-5

    authors: Şişli E,Tuncer ON,Şenkaya S,Doğan E,Şahin H,Ayık MF,Atay Y

    更新日期:2019-01-01 00:00:00

  • Evaluation of Impedance Cardiography for Measurement of Stroke Volume in Congenital Heart Disease.

    abstract::Noninvasive measurement of cardiac output (CO) and particularly stroke volume (SV) remain difficult but potentially valuable. These variables can be particularly challenging to measure in children with congenital heart disease (CHD). Impedance cardiography (IC) is a technique shown to be accurate in measuring SV in ad...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-016-1456-x

    authors: Ebrahim M,Hegde S,Printz B,Abcede M,Proudfoot JA,Davis C

    更新日期:2016-12-01 00:00:00

  • Endogenous dilator prostaglandins in congenital heart disease.

    abstract::Maintaining patency of the ductus arteriosus pending surgical intervention can be critical to the survival of the neonate with ductal dependent congenital heart disease. Spontaneously delayed ductal closure has been observed clinically and experimentally in newborns with critical pulmonic stenosis. Infants with ductal...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/BF02263445

    authors: Hammerman C,Aramburo MJ,Bui KC

    更新日期:1987-01-01 00:00:00

  • Isolated innominate artery as a cause of subclavian steal and cerebral hemisphere atrophy.

    abstract::A rare case of isolated innominate artery arising from a left persistent arterial duct with a right aortic arch is presented. Of interest in this case is the retrograde flow in the left carotid system, the history of developmental delay, and the magnetic resonance image (MRI) brain findings suggestive of asymmetric vo...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-010-9739-0

    authors: Reeves BM,Colen TM,Sheridan BJ,Ward C

    更新日期:2010-10-01 00:00:00

  • Double-outlet single ventricle and an abdominal vascular mass: in utero diagnosis with pathological confirmation.

    abstract::A fetal echocardiographic scan was performed when routine prenatal ultrasound screening failed to identify four cardiac chambers. The scan showed a single ventricle with an associated circoid varicosity. Because of these anomalies, amniocentesis was suggested and trisomy 18 confirmed. The presence of major cardiac str...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/BF00794843

    authors: Duncan WJ,George D,Ezzat W,Wallace K,Van den Beuken B

    更新日期:1993-01-01 00:00:00

  • Surgical cutdown of the right carotid artery for aortic balloon valvuloplasty in infancy: midterm follow-up.

    abstract::A vascular approach for balloon aortic dilatation in infants is of major concern due to the high risk of femoral artery injury. To overcome this problem, a surgical right carotid artery (RCA) approach has been advocated. No reports are available on RCA after neonatal cutdown. Since 1990, RCA cutdown has been performed...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s002460010202

    authors: Borghi A,Agnoletti G,Poggiani C

    更新日期:2001-05-01 00:00:00

  • Beta-blocker therapy failures in symptomatic probands with genotyped long-QT syndrome.

    abstract::Beta-blocker therapy is one of the principal therapies for congenital long-QT syndrome (LQTS). However, breakthrough cardiac events occur while being treated with beta-blockers. We sought to determine the frequency of and clinical correlates underlying beta-blocker therapy failures in genotyped, symptomatic LQTS proba...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-003-0567-3

    authors: Chatrath R,Bell CM,Ackerman MJ

    更新日期:2004-09-01 00:00:00

  • Serum Sirolimus Levels After Implantation of Third Generation Drug Eluting Cobalt Chromium Coronary Stent in Ductus Arteriosus in Neonates with Duct-Dependent Pulmonary Circulation.

    abstract::Ductal stenting (DS) palliates duct-dependent lesions using coronary stents. Sirolimus-eluting stents have replaced bare-metal stents in coronary interventions. Concerns exist about sirolimus levels in neonates. Therapeutic immunosuppressive sirolimus level is 5-15 ng/ml. After neonatal DS, drug levels were assessed a...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-020-02381-4

    authors: Sivakumar K,Pavithran S,Sonawane B,Rajendran M,Ramasamy R

    更新日期:2020-10-01 00:00:00

  • Balloon angioplasty and stent implantation performed through systemic-to-pulmonary artery shunts in infants and neonates.

    abstract::Branch pulmonary artery stenosis (BPAS) in the setting of systemic-pulmonary artery shunts (SPS) may result in significant sequelae. Limited information exists regarding the safety and efficacy of pulmonary artery balloon angioplasty and stent implantation via SPS in neonates and infants. This study aimed to examine t...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-013-0657-9

    authors: Aregullin EO,Gutierrez Y,Osorio S,Nykanen DG,Khan DM,Zahn EM

    更新日期:2013-08-01 00:00:00

  • An old autopsy report sheds light on a "new" disease: infantile polyarteritis nodosa and kawasaki disease.

    abstract::Although Kawasaki disease (KD) was first discovered and identified in Japan by Kawasaki in the 1960s, fatal KD cases resulting from coronary artery aneurysms had been identified retrospectively in the West as early as 1871. Kawasaki initially postulated that this disease was a new, as yet unidentified, self-limiting i...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-009-9625-9

    authors: Kushner HI,Abramowsky CR

    更新日期:2010-05-01 00:00:00

  • Evolution of Ventricular Energetics in the Different Stages of Palliation of Hypoplastic Left Heart Syndrome: A Retrospective Clinical Study.

    abstract::Hyperplastic left heart syndrome (HLHS) patients are palliated by creating a Fontan-type circulation passing from different surgical stages. The aim of this work is to describe the evolution of ventricular energetics parameters in HLHS patients during the different stages of palliation including the hybrid, the Norwoo...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-017-1704-8

    authors: Di Molfetta A,Iacobelli R,Guccione P,Di Chiara L,Rocchi M,Cobianchi Belisari F,Campanale M,Gagliardi MG,Filippelli S,Ferrari G,Amodeo A

    更新日期:2017-12-01 00:00:00

  • An Alternative Strategy for Bridge-to-Transplant/Recovery in Small Children with Dilated Cardiomyopathy.

    abstract::Dilated cardiomyopathy in children still has a poor prognosis with high rates of mortality and cardiac transplantation (resp. around 20 and 25%). Awaiting transplantation or possible recovery, these pediatric patients are mechanically supported with extracorporeal membrane oxygenation or a paracorporeal ventricular as...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章,评审

    doi:10.1007/s00246-017-1610-0

    authors: Mets G,Panzer J,De Wolf D,Bové T

    更新日期:2017-06-01 00:00:00