Annals of Pediatric Cardiology
About us | Current Issue | Archives | Ahead of Print | Instructions | Submission | Subscribe | Advertise | Contact | Reader Login
  Instructions 
  Search 
  My preferences 

 


Export selected to
Endnote
Reference Manager
Procite
Medlars Format
RefWorks Format
BibTex Format
  Access statistics : Table of Contents
   2012| July-December  | Volume 5 | Issue 2  
    Online since August 11, 2012

 
 
  Archives   Previous Issue   Next Issue   Most popular articles   Most cited articles
 
Hide all abstracts  Show selected abstracts  Export selected to
  Viewed PDF Cited
REVIEW ARTICLE
The use of Z-scores in paediatric cardiology
Henry Chubb, John M Simpson
July-December 2012, 5(2):179-184
DOI:10.4103/0974-2069.99622  PMID:23129909
Z-scores are a means of expressing the deviation of a given measurement from the size or age specific population mean. By taking account of growth or age, Z-scores are an excellent means of charting serial measurements in paediatric cardiological practice. They can be applied to echocardiographic measurements, blood pressure and patient growth, and thus may assist in clinical decision-making.
  14,293 1,034 18
CASE REPORTS
Carotid-subclavian bypass for subclavian steal syndrome following coarctation repair in infancy
Scott Chowning, Donald Stowell, UmaKumaran Ponniah
July-December 2012, 5(2):207-209
DOI:10.4103/0974-2069.99631  PMID:23129918
A 19 year old man presented with dizziness that was exacerbated while using left arm. On investigation, subclavian steal syndrome (SSS) was diagnosed. He underwent left carotid to subclavian bypass with relief of symptoms. Subclavian steal syndrome, although rare, should be considered in the differential diagnosis in patients with the history of subclavian artery manipulation in the past in proper settings.
  10,712 148 -
POINT OF VIEW
Rheumatic fever pathogenesis: Approach in research needs change
Rajendra Tandon
July-December 2012, 5(2):169-178
DOI:10.4103/0974-2069.99621  PMID:23129908
Despite identifying that rheumatic fever (RF) is the result of an immunological reaction following group-A beta-hemolytic streptococcal infection, the pathogenesis remains elusive. RF has been incorrectly designated as causing pancarditis, since it does not cause myocarditis. Research directed toward myocarditis, targeting myosin to unravel the pathogenesis has not succeeded in more than 60 years. RF causes permanent damage to cardiac valves. The mitral valve (MV), derived from the wall of the left ventricle, is composed of a central core of connective tissue, covered on both sides by endothelium. The left ventricle does not have either myocardial or intermyocardial connective tissue involvement in RF. By exclusion, therefore, the primary site of RF damage appears to be the endothelium. Evaluation of the histopathology and immunopathology indicates that RF is a disease of the valvular and vascular endothelium. It is not a connective tissue disorder. Research to identify pathogenesis needs to be focused toward valvular endothelium.
  9,296 707 5
ORIGINAL ARTICLE
Transcatheter closure of large patent ductus arteriosus with severe pulmonary arterial hypertension: Short and intermediate term results
Parag S Bhalgat, Robin Pinto, Bharat V Dalvi
July-December 2012, 5(2):135-140
DOI:10.4103/0974-2069.99614  PMID:23129901
Objective: To assess the efficacy and safety of transcatheter closure (TCC) of patent ductus arteriosus (PDA) with severe pulmonary arterial hypertension (PHT). Background: TCC of small and moderate-sized PDAs is well established. However, there is a paucity of data on TCC of large PDA with severe PHT. Methods: This is a retrospective observational study of 76 patients with large PDA and severe PHT who were referred for TCC. Multiple clinical and investigational parameters were evaluated to decide the reversibility of PHT. Following the TCC, patients were serially followed up to assess the efficacy and safety of closure and its impact on PHT. Results: Of 76 patients, nine were found to have PDA with Eisenmenger's syndrome. Of remaining 67, two were thought to have irreversible PHT based on hemodynamic data obtained after balloon occlusion of the duct. Sixty five patients, who eventually underwent TCC of PDA, had a median age of 9.1 years (range 1 month to 40 years). The weight ranged between 2.5 to 62 kg (median 14 kg). The PDA size was 9.1 ± 4.6 mm. The mean systolic pulmonary artery pressure was 66.9 ± 15.3 mm Hg. Duct occluder was used in 63 and muscular ventricular septal defect closure device in 2. The follow up was available in 56 (86%) with a mean follow up period of 65 ± 34 months. All the patients had complete closure of the PDA at 6 months follow up. Mild obstruction of left pulmonary artery (n=3) and aortic isthmus flow (n=6) was noted at the time of discharge. During the follow up, partial or complete resolution of PHT was observed in all the patients in whom Doppler-derived right ventricular systolic pressure was recorded (available in 40 of 56 patients). Conclusions: TCC of large PDA with severe PHT and significant left to right shunt was found to be effective and safe in the short and intermediate term.
  3,728 498 5
IMAGES
A giant left atrial appendage aneurysm with a large pinball-like thrombus in a 2 year old
Simarjot Singh Sarin, Tripat Bindra, Gurpreet S Chhabra
July-December 2012, 5(2):215-216
DOI:10.4103/0974-2069.99634  PMID:23129921
Congenital left atrial appendage aneurysm is very rare. We describe a giant left atrial appendage aneurysm with a pinball-like mobile thrombus in a 2-year-old child with cardioembolic stroke. Patient underwent successful surgical resection of the aneurysm.
  3,241 190 2
CASE REPORTS
Unexpected difficulty during transcatheter device closure of atrial septal defect associated with right aortic arch
Nageswara Rao Koneti, Abhijeet Shelke, Srinivasa Kumar Arramraj, Raghava Raju Penumatsa
July-December 2012, 5(2):185-187
DOI:10.4103/0974-2069.99623  PMID:23129910
Right aortic arch (RAA) associated with isolated atrial septal defect (ASD) is very rare. We report successful closure of ASD associated with RAA using a 26-mm atrial septal occluder in a 30-year-old male patient. The impingement of right descending aorta in RAA caused malposition of the device in the left atrium. Deployment of the device through the right upper pulmonary vein successfully closed the defect. Follow-up evaluation by computerized tomography scan and echocardiogram showed no pulmonary venous obstruction.
  3,046 171 -
ORIGINAL ARTICLE
Cardiac involvement in Kawasaki disease in Pakistani children
Saleem Akhtar, Muhammad Matloob Alam, Mehnaz Atiq Ahmed
July-December 2012, 5(2):129-132
DOI:10.4103/0974-2069.99612  PMID:23129899
Introduction: Coronary artery involvement is the most dreaded long-term complication of Kawasaki disease. Our aim was to look at the pattern of cardiovascular involvement in Pakistani children admitted with Kawasaki disease. Methods: This study included children admitted with Kawasaki disease at the Aga Khan University Hospital Karachi over a period of 14 years from January 1997 to December 2010. Information gathered included patient demographics, clinical features, investigations, echocardiographic findings, treatment and follow-up. Those with coronary artery involvement on initial echocardiogram remained on long-term follow-up with clinical examination and echocardiogram. Results: A total of 56 patients were admitted. (Mean age at diagnosis 33 ± 30 months, age range 2 months to 9 years). 18% of patients had incomplete features. Twenty-five percent (14/56) patients presented after 10 days of fever. Cardiac examination was normal except for tachycardia. Abnormal coronary arteries were seen in 23 patients (41%) - left main coronary artery in 23 (41%), left anterior descending and right main coronary artery in 20 (36%), circumflex branch in 17 (30%). Risk factors for cardiac involvement were male sex, fever >10 days duration at the time of initial presentation and neutrophil percentage >75% in the initial white blood cell counts. Fifty four of 56 cases received intravenous immunoglobulin (IVIG), Seventy-five percent of the patients received IVIG within 10 days of illness. Mean duration of follow-up was 2.5 years. Eight percent of the patients still continue to have abnormal coronaries. There was no mortality. Conclusions: A higher incidence of coronary artery involvement was found in our study. Presentation after 10 days of illness increases the risk of coronary artery involvement. High index of suspicion among the general pediatricians about the disease can possibly be helpful for early referral and treatment.
  2,852 312 3
IMAGES
Lung herniation into pericardial cavity: A case of partial congenital absence of right pericardium
Sadashiv B Tamagond, Saket Agarwal, Akhilesh S Tomar, Deepak K Satsangi
July-December 2012, 5(2):213-214
DOI:10.4103/0974-2069.99633  PMID:23129920
Congenital absence of pericardium is rarely seen, often diagnosed intraoperatively during cardiac and thoracic surgeries. Left-sided pericardial defects are more common than right-sided ones. We present a case of an incidentally detected congenital absence of right pericardium with herniation of part of the right lung during ventricular septal defect closure surgery in a male child aged 4 years.
  3,031 121 1
CASE REPORTS
Total anomalous pulmonary venous connection with descending vertical vein: Unusual drainage to azygos vein
Saurabh Kumar Gupta, Gurpreet Singh Gulati, Rajnish Juneja, Velayoudam Devagourou
July-December 2012, 5(2):188-190
DOI:10.4103/0974-2069.99624  PMID:23129911
Most patients with total anomalous pulmonary venous connection have a set pattern of pulmonary venous drainage and predictable sites of obstruction. However, uncommon variations do exist and delineating the entire course is more important than just knowing the site of drainage. Azygos vein involvement in the circuit is nearly always associated with a complicated course, as was seen in our patient. This report reviews the drainage patterns when azygos vein forms a part of the circuit.
  2,734 191 -
Use of an active fixation lead and a subpectoral pacemaker pocket may not avoid Twiddler's syndrome
Floris E A Udink ten Cate, Roland Adelmann, Beate E Schmidt, Narayanswami Sreeram
July-December 2012, 5(2):203-204
DOI:10.4103/0974-2069.99629  PMID:23129916
Manipulation of a pacemaker with consequent malfunction of the device has been called Twiddler's syndrome. Use of active-fixation leads and subpectoral pacemaker pockets has been considered to help in avoiding this problem. We describe a child in whom twiddling was not prevented despite implantation of a lumenless atrial lead and insertion of the pacemaker generator in a subpectoral pocket.
  2,816 98 3
EDITORIAL
Evolution of an idea: The case of prophylaxis against infective endocarditis
Shyam S Kothari
July-December 2012, 5(2):117-119
DOI:10.4103/0974-2069.99608  PMID:23129896
  2,518 357 -
CASE REPORTS
A rare association with patent ductus arteriosus
Dhanya Warrier, Sejal Shah, Colin John, L Dayananda
July-December 2012, 5(2):191-193
DOI:10.4103/0974-2069.99625  PMID:23129912
Persistent fifth aortic arch (PFAA), also known as congenital double-lumen aortic arch, is a rare developmental anomaly of the aortic arch. A 5-month-old baby who presented with congestive cardiac failure was diagnosed to have a large patent ductus arteriosus with PFAA. Although this arch anomaly had no hemodynamic relevance in this case, preoperative diagnosis prevented surprises "on table."
  2,616 209 3
Idiopathic isolated annular dilatation causing congenital mitral regurgitation
Lalitaditya Malik, Anubhav Gupta, Ranjit Kumar Nath, Vijay Grover, Vijay Kumar Gupta
July-December 2012, 5(2):200-202
DOI:10.4103/0974-2069.99628  PMID:23129915
Isolated annular dilatation is an extremely uncommon cause of congenital mitral regurgitation. We report a case of a 5-year-old child with idiopathic isolated annular dilatation causing severe congenital mitral regurgitation.
  2,659 123 -
ORIGINAL ARTICLE
Prognostic value of clinical and Doppler echocardiographic findings in children and adolescents with significant rheumatic valvular disease
Fátima Derlene da Rocha Araújo, Eugęnio Marcos Andrade Goulart, Zilda Maria Alves Meira
July-December 2012, 5(2):120-126
DOI:10.4103/0974-2069.99610  PMID:23129897
Introduction: The diagnosis of acute rheumatic fever (RF) is based on clinical findings. However, during the chronic phase of the disease, the clinical approach is not sufficient for the follow-up of the patients and the Doppler echocardiography is a tool for the diagnosis of cardiac involvement. Prognostic variables that influence long-term outcomes are not well known. Methods: 462 patients with RF according to Jones criteria were studied, and followed-up from the initial attack to 13.6 ± 4.6 years. All patients underwent clinical assessment and Doppler echocardiography for the detection of heart valve involvement in the acute and chronic phases. Multivariate logistic regression analysis was used to identify the factors influencing long-term heart valve disease. Results: Carditis occurred in 55.8% and subclinical valvulitis in 35.3% patients. In the chronic phase, 33% of the patients had significant valvular heart disease. No normal Doppler echocardiography exam was observed on patients who had severe valvulitis, although heart auscultation had become normal in 13% of these. In the multivariate analysis, only the severity of carditis and the mitral and/or aortic valvulitis were associated with significant valvular heart disease. Chorea or arthritis were protective factors for significant valvular heart disease, odds ratio 0.41 (95% C.I. 0.22 - 0.77) and 0.43 (95% C.I. 0.23 - 0.82), respectively. Conclusions: Our study suggests that the use of Doppler echocardiography during RF helps to identify prognostic factors regarding the development of significant valvular heart disease. Initial severe carditis is an important factor in the long-term prognosis of chronic RHD, whereas arthritis and chore during the initial episode of RF appears to be protective. Strict secondary prophylaxis should be mandatory in high risk patients.
  2,131 594 3
INVITED COMMENT
Diagnosis of acute rheumatic carditis: An echo in time…
Ganesan Karthikeyan
July-December 2012, 5(2):127-128
  2,260 437 -
Finding Kawasaki disease
Jane C Burns
July-December 2012, 5(2):133-134
PMID:23129900
  2,364 275 -
Large patent ductus arteriosus: To close or not to close
Jaganmohan Tharakan, Subramanian Venkateshwaran
July-December 2012, 5(2):141-144
PMID:23129902
  2,167 392 -
ORIGINAL ARTICLES
Effect of ventricular size and function on exercise performance and the electrocardiogram in repaired tetralogy of Fallot with pure pulmonary regurgitation
Shaji C Menon, Aditya K Kaza, Michael D Puchalski
July-December 2012, 5(2):151-155
DOI:10.4103/0974-2069.99617  PMID:23129904
Background: In repaired tetralogy of Fallot (TOF), exercise test parameters like peak oxygen uptake and ventilatory efficiency predict mortality. Studies have also suggested cardiac magnetic resonance (CMR)-derived right ventricular (RV) size threshold values for pulmonary valve replacement in repaired TOF. However, effects of proposed RV size on exercise capacity and morbidity are not known. Methods: The relationship between CMR-derived ventricular size, function, and pulmonary regurgitation (PR) and NYHA class, exercise performance, and electrocardiogram (ECG) was studied in patients of repaired TOF with pure PR in a retrospective review of records. Results: 46 patients (22 females), mean age 14 years (8−30.8), were studied. There was no relationship between CMR-derived ventricular size, function, or PR and exercise test parameters, or NYHA class. RV end systolic and end diastolic volume correlated positively with the degree of PR. QRS duration on ECG correlated positively with RV end-diastolic volume (P < 0.01, r2 = 0.34) and PR (P < 0.01, r2 = 0.52). Conclusions: In repaired TOF and pure PR, there is no correlation between ventricular size or function and exercise performance. RV size increases with increasing PR. Timing of pulmonary valve replacement in TOF with pure PR needs further prospective evaluation for its effect on morbidity and mortality.
  2,257 213 6
Palliative stent implantation for coarctation in neonates and young infants
Isabel Sreeram, Narayanswami Sreeram, Gerardus Bennink
July-December 2012, 5(2):145-150
DOI:10.4103/0974-2069.99616  PMID:23129903
Background: In selected neonates and infants, primary palliative stent implantation may be indicated for coarctation of the aorta. We describe our experience with this approach in five consecutive patients. Methods: Five neonates and infants (age range 6 to 68 days, gestation 33 to 38 weeks, weight range at procedure of between 1650 to 4000 g) underwent palliative stent implantation as primary therapy for coarctation of the aorta. Indications for primary stent implantation were varied. All procedures were performed by elective surgical cut down of the axillary artery. Standard coronary stents (diameter 4.5 to 5 mm, length 12 to 16 mm) were delivered via a 4F sheath. The axillary artery was repaired after removal of the sheath. Results: All procedures were acutely successful, and without procedural complications. All patients survived to hospital discharge. Four patients have subsequently undergone elective stent removal and surgical repair of the arch, at between 38 and 83 days following stent implantation. Complete stent removal was achieved in three patients. Over a follow-up ranging between 8 weeks and 36 months, none of the patients has had any further complications. Conclusions: This palliative approach is warranted in carefully selected patients. Long-term follow-up is required.
  2,252 206 2
CASE REPORTS
Infective endarteritis and false mycotic aneurysm complicating aortic coarctation
Ziadi Jaleleddine, Chatti Sana, Ghedira Faker, Khayati Adel
July-December 2012, 5(2):197-199
DOI:10.4103/0974-2069.99627  PMID:23129914
A 12-year-old boy with coarctation of aorta developed infective endarteritis and mycotic aneurysm at the site distal to coarctation. The computed tomography angiogram was very helpful in the diagnosis. Medical management and early surgical intervention was curative. Infective endarteritis in coarctation may be underdiagnosed.
  2,227 157 3
BRIEF COMMUNICATIONS
Awareness of fetal echo in Indian scenario
Dhanya Warrier, Rahul Saraf, Sunita Maheshwari, PV Suresh, Sejal Shah
July-December 2012, 5(2):156-159
DOI:10.4103/0974-2069.99618  PMID:23129905
Background: Fetal echocardiography is a well established sensitive tool to diagnose congenital heart disease (CHD) in utero. One of the determinants of effective utilization of fetal echocardiography is its awareness in the general population. The present hospital based study was undertaken to assess the awareness of the need for fetal echocardiography amongst Indian parents. Methods: One thousand one hundred and thirty eight consecutive parents who visited the pediatric cardiology outpatient department of a tertiary care centre over a period of two months were asked to fill up a questionnaire that included their demographic data, educational status, history of CHD in children, awareness of fetal echocardiography and source of information and timing of fetal echocardiogram if performed. The data was categorized and awareness was noted in different groups. Results: The awareness in the study population was 2.2%. Awareness was found to be similar across the study population irrespective of the demographics and high risk status of the parents. Conclusions: The awareness of fetal echocardiography, an important tool in reducing the incidence of complex CHD, thereby impacting public health, is alarmingly low in the population studied. Appropriate action to increase awareness of fetal echocardiography needs to be looked into.
  2,195 182 1
CASE REPORTS
Transcatheter interruption of large residual flow after device closure of "Type A" patent ductus arteriosus
Anuradha Sridhar, Raghavan Subramanyan, Premsekar Rajasekar
July-December 2012, 5(2):210-212
DOI:10.4103/0974-2069.99632  PMID:23129919
We report a case of 3-year-old girl who had persistence of large residual flow following transcatheter closure of a 6 mm 'Type A' patent ductus arteriosus using a 12 × 10 mm duct occluder. Angiography revealed a large left-to-right shunt coursing through and exiting around the implanted device. Near total abolition of the residual shunt was achieved by initial implantation of an embolization coil within the duct occluder and subsequently an Amplatzer duct occluder (ADO II) adjacent to the duct occluder. This challenging case describes an additional technique of abolishing a large residual flow in and around a Nitinol duct occluder device.
  2,119 154 -
Myocardial ischemia following arterial switch operation: An uncommon etiology
R Saileela, C Shanthi, Krishna Manohar, Raghavan Subramanyan, KM Cherian
July-December 2012, 5(2):194-196
DOI:10.4103/0974-2069.99626  PMID:23129913
Myocardial ischemia following arterial switch operation (ASO) usually occurs due to coronary ostial narrowing that might result from technical failure in translocation of the coronary arteries to the neoaorta. We present an unusual case report of neonatal myocardial ischemia caused by coronary steal secondary to aortopulmonary collaterals, following ASO in transposition of great arteries.
  2,063 136 -
BRIEF COMMUNICATIONS
Safety and usefulness of outreach clinic conducted by pediatric echosonographers
Badr Al Harbi, Ali A Al Akhfash, Abdullah Al Ghamdi, Abdulrahman Al-Mesned
July-December 2012, 5(2):165-168
DOI:10.4103/0974-2069.99620  PMID:23129907
Background: Outreach echocardiographic services led by cardiac sonographers may help district level hospitals in the management of patients suspected to have cardiac anomalies. However, the safety and utility of such an approach is not tested. Methods: We retrospectively reviewed our experience of patients seen in the outreach visits by the echocardiographers alone and subsequently reviewed in the pediatric cardiology clinic. Comparison between the diagnosis made by the echocardiographer and the consultant pediatric cardiologist were done. We defined safety as no change in patient management plan between the outreach evaluation and the pediatric cardiology clinic evaluation, and we defined usefulness as being beneficial, serviceable and of practical use. Results: Two senior echocardiographic technicians did 41 clinic visits and over a period of 17 months, 623 patients were seen. Patients less than 3 months of age constitute 63% of the total patients seen. Normal echocardiographic examinations were found in 342 (55%) of patients. These patients were not seen in our cardiology clinic. Abnormal echocardiographic examinations were found in 281 (45%) of patients. Among the 281 patients with abnormal echos in the outreach visits, 251 patients (89.3%) were seen in the pediatric cardiology clinic. Comparing the results of the outreach clinic evaluation to that of the pediatric cardiology clinic, 73 patients (29%) diagnosed to have a minor CHD turned to have normal echocardiographic examinations. In all patients seen in both the outreach clinics and the pediatric tertiary cardiac clinics there was no change in patient's management plan. Conclusions: Outreach clinic conducted by pediatric echo sonographers could be useful and safe. It may help in reducing unnecessary visits to pediatric cardiology clinics, provide parental reassurance, and help in narrowing the differential diagnosis in critically ill patient unable to be transferred to tertiary cardiac centers provided it is done by experienced echosonographers.
  2,053 122 1
CASE REPORTS
Factor V Leiden mutation: An added risk in single ventricle palliation
R Saileela, C Shanthi, Ravi Agarwal, Raghavan Subramanyan, KM Cherian
July-December 2012, 5(2):205-206
DOI:10.4103/0974-2069.99630  PMID:23129917
We present the case report of a child with Factor V Leiden mutation who underwent Fontan procedure. Thromboembolism is a widely recognized complication of the Fontan procedure and its modifications. Factor V Leiden mutation, being a hypercoagulable state, posed a higher risk for thromboembolism in this child. Appropriate measures taken before and after surgery prevented postoperative coagulopathy.
  1,873 101 -
BRIEF COMMUNICATIONS
Endothelial dysfunction and atherosclerosis in children with irreversible pulmonary hypertension due to congenital heart disease
Murat Ciftel, Ayse Simsek, Özlem Turan, Firat Kardelen, Gayaz Akçurin, Halil Ertug
July-December 2012, 5(2):160-164
DOI:10.4103/0974-2069.99619  PMID:23129906
Objective: To assess endothelial dysfunction and the risk for coronary atherosclerosis in children with irreversible pulmonary hypertension due to congenital heart disease (CHD). Methods: The study included 18 cyanotic patients (the mean age was 12.28 ± 3.26 years) who developed irreversible pulmonary hypertension due to cyanotic and acyanotic CHDs, and 18 control patients (the mean age was 11.78 ± 3.00 years). Study groups were compared for flow-mediated dilatation (FMD), carotid intima media thickness (CIMT) and atherosclerotic risk factors. Results: Compared to the control group, the mean FMD was significantly reduced in the cyanotic group (5.26 ± 2.42% and 9.48 ± 2.60%, respectively; P-value < 0.001). No significant difference was observed between the groups in CIMT (0.41 ± 0.08 mm and 0.39 ± 0.06 mm, respectively; P-value = 0.299). The levels of total cholesterol, low-density lipoprotein-cholesterol and very low-density lipoprotein-cholesterol were statistically significantly lower compared tothe control group (P-value = 0.001, 0.006 and 0.014, respectively), whereas no statistically significant difference was found in the levels of high-density lipoprotein-cholesterol and triglycerides (P-value = 0.113 and 0.975, respectively). Conclusions: Systemic endothelial dysfunction in children with irreversible pulmonary hypertension due to CHD was noted but there was no increased risk for atherosclerosis.
  1,445 174 -
SELECTED SUMMARIES
Selected summaries
Sachin Talwar, Anil K Singhi
July-December 2012, 5(2):217-219
  1,284 107 -