Full Text Journal Articles about
Valvar Pulmonary Stenosis

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Mitral Valve Repair in Young Rheumatic Patients.

Pablo Maria Alberto Pomerantzeff,

Arq. Bras. Cardiol. (Arquivos brasileiros de cardiologia)
[2019, 113(4):757]

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EDUCATIONAL SERIES IN CONGENITAL HEART DISEASE: Echocardiographic assessment of transposition of the great arteries and congenitally corrected transposition of the great arteries

Meryl S Cohen, Luc L Mertens,

Echocardiographic assessment of patients with transposition of the great arteries and congenitally corrected transposition requires awareness of the morphology and commonly associated lesions. The pre-operative echocardiography should include a full segmental and sequential analysis. Post-operative assessment is not possible without awareness of the type of surgical procedure performed and consists ... Read more >>

Echo Res Pract (Echo research and practice)
[2019, 6(4):R107-R119]

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Costello Syndrome

Karen W Gripp, Katherine A Rauen,

CLINICAL CHARACTERISTICS:While the majority of individuals with Costello syndrome share characteristic findings affecting multiple organ systems, the phenotypic spectrum is wide, ranging from a milder or attenuated phenotype to a severe phenotype with early lethal complications. Costello syndrome is typically characterized by failure to thrive in infancy as a result ... Read more >>

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Caught-off guard: Unguarded mitral valve orifice in usual atrial arrangement with discordant atrioventricular connections and pulmonary atresia.

Nayan Banerji, Mani Ram Krishna, Raman Krishna Kumar, Robert H Anderson,

Unguarding of an atrioventricular valvar orifice is a rare form of congenital heart disease that requires staged functionally univentricular palliation. Unguarding of the mitral valvar orifice has previously been reported in the setting of mirror-imaged atrial arrangement. We report a neonate with unguarding of the mitral valvar orifice in the ... Read more >>

Ann Pediatr Cardiol (Annals of pediatric cardiology)
[2020, 13(1):84-86]

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Rare Association of Absent Pulmonary Valve Syndrome with Double Outlet Right Ventricle and Hypoplastic Left Heart Complex.

Erik L Frandsen, Arpan R Doshi, Sujatha Buddhe, Bhawna Arya, Sathish M Chikkabyrappa,

Kans J Med (Kansas journal of medicine)
[2020, 13:21-22]

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Congenital supravalvular and subvalvular pulmonary stenosis with hypoplastic pulmonary annulus associated with congenital rubella syndrome.

Dibbendhu Khanra, Yash Shrivastava, Bhanu Duggal, Shishir Soni,

BMJ Case Rep (BMJ case reports)
[2019, 12(7):]

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Double-Outlet Left Ventricle: The Importance of Echocardiographic and Computed Tomographic Assessment.

Ezequiel Sagray, M Yasir Qureshi, Thomas A Foley, Donald J Hagler, Patrick W O'Leary, Frank Cetta,

CASE (Phila) (CASE (Philadelphia, Pa.))
[2019, 3(4):141-144]

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Ultimate Third Heart Sound.

Ayu Shono, Shumpei Mori, Atsusuke Yatomi, Tsubasa Kamio, Jun Sakai, Fumitaka Soga, Hidekazu Tanaka, Ken-Ichi Hirata,

A 79-year-old man with dilated cardiomyopathy and severe functional mitral regurgitation presented with general fatigue and dyspnea. Auscultation revealed a systolic regurgitant murmur with a minimized second heart sound due to a low output. On the other hand, the third heart sound was ultimately enhanced, being visible and palpable as ... Read more >>

Intern. Med. (Internal medicine (Tokyo, Japan))
[2019, 58(17):2535-2538]

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Tetralogy of Fallot: morphological variations and implications for surgical repair.

Saad M Khan, Nigel E Drury, John Stickley, David J Barron, William J Brawn, Timothy J Jones, Robert H Anderson, Adrian Crucean,

OBJECTIVES:Tetralogy of Fallot is characterized by anterocephalad deviation of the outlet septum, along with abnormal septoparietal trabeculations, which lead to subpulmonary infundibular stenosis. Archives of retained hearts are an important resource for improving our understanding of congenital heart defects and their morphological variability. This study aims to define variations in ... Read more >>

Eur J Cardiothorac Surg (European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery)
[2019, 56(1):101-109]

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More than numbers: preprocedural multislice computed tomography analysis in a patient undergoing transcatheter aortic valve implantation.

Kerstin Piayda, Katharina Hellhammer, Oliver Maier, Verena Veulemans,

Multislice computed tomography (MSCT) has emerged as an integral part of patient evaluation in transcatheter aortic valve implantation (TAVI). Beyond sizing, it offers valuable information especially in challenging anatomies and helps to provide accurate dimensions and highlight potential pitfalls. We present the case of a 94-year-old woman with a coronary ... Read more >>

BMJ Case Rep (BMJ case reports)
[2019, 12(6):]

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Anesthesia in the Form of Audiovisual Distraction for a Child Requiring Surgery With End-Stage Cardiomyopathy: A Case Report.

Adam C Adler, Tamer Elattary, Arvind Chandrakantan,

Anesthetizing children with extreme cardiopulmonary illness can be especially challenging. In adults, a host of alternatives to general anesthesia for the labile patient are available, However, in children, these techniques may be challenging due to a lack of patient cooperation. Distraction techniques have been successfully used to reduce procedural pain. ... Read more >>

A A Pract (A&A practice)
[2019, 13(9):346-349]

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Successful balloon valvuloplasty of a subpulmonic membrane associated with cor triatriatum dexter: a case report.

Meryem Haboub, Abdenasser Drighil,

BACKGROUND:Subpulmonic membrane as a cause of right ventricular outflow tract obstruction in patients with concordant ventriculoarterial connection and intact ventricular septum is considered to be rare. Association with cor triatriatum dexter and success of subpulmonic balloon valvuloplasty have never been reported, at least to the best of our knowledge. CASE ... Read more >>

J Med Case Rep (Journal of medical case reports)
[2019, 13(1):291]

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Management of Congenital Heart Disease: State of the Art; Part I-ACYANOTIC Heart Defects.

P Syamasundar Rao,

Since the description of surgery for patent ductus arteriosus in late 1930s, an innumerable number of advances have taken place in the management of congenital heart defects (CHDs). In this review the current status of treatment of seven of the most common acyanotic CHDs was reviewed. The discussion included indications ... Read more >>

Children (Basel) (Children)
[2019, 6(3):]

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Prevalence of Noonan spectrum disorders in a pediatric population with valvar pulmonary stenosis.

Kailyn Anderson, James Cnota, Jeanne James, Erin M Miller, Ashley Parrott, Valentina Pilipenko, Kathryn Nicole Weaver, Amy Shikany,

OBJECTIVE:To evaluate the prevalence of Noonan spectrum disorders (NSD) in a pediatric population with valvar pulmonary stenosis (vPS) and identify the clinical characteristics that differentiate those with NSD from those without NSD. DESIGN:A retrospective chart review of 204 patients diagnosed with vPS between 9/1/2012 and 12/1/2016 at a pediatric medical ... Read more >>

Congenit Heart Dis (Congenital heart disease)
[2019, 14(2):264-273]

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Management of Congenital Heart Disease: State of the Art-Part II-Cyanotic Heart Defects.

P Syamasundar Rao,

In this review management of the most common cyanotic congenital heart defects (CHDs) was discussed; the management of acyanotic CHD was reviewed in Part I of this series. While the need for intervention in acyanotic CHD is by and large determined by the severity of the lesion, most cyanotic CHDs ... Read more >>

Children (Basel) (Children)
[2019, 6(4):]

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Pregnancy in Women with Complex Congenital Heart Disease. A Constant Challenge.

Walkiria Samuel Avila, Veronica Martins Ribeiro, Eduardo Giusti Rossi, Maria Angelica Binotto, Maria Rita Bortolotto, Carolina Testa, Rossana Francisco, Ludhmilla Abraão Hajjar, Nana Miura,

BACKGROUND:The improvement in surgical techniques has contributed to an increasing number of childbearing women with complex congenital heart disease (CCC). However, adequate counseling about pregnancy in this situation is uncertain, due to a wide variety of residual cardiac lesions. OBJECTIVES:To evaluate fetal and maternal outcomes in pregnant women with CCC ... Read more >>

Arq. Bras. Cardiol. (Arquivos brasileiros de cardiologia)
[2019, 113(6):1062-1069]

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Fetal cardiomyopathy in neurofibromatosis type I: Novel phenotype and review of the literature.

Alyssa Ritter, Sanmati Cuddapah, Karl Degenhardt, Stefanie Kasperski, Mark P Johnson, Matthew J O'Connor, Rebecca Ahrens-Nicklas,

Neurofibromatosis type I (NF1) is a relatively common genetic disorder characterized by neurocutaneous lesions, neurofibromas, skeletal anomalies, iris hamartomas, and predisposition to other tumors. NF1 results from heterozygous loss-of-function mutations in neurofibromin (NF1), and diagnosis is most often made using clinical diagnostic criteria. Cardiac manifestations of NF1 include congenital heart ... Read more >>

Am. J. Med. Genet. A (American journal of medical genetics. Part A)
[2019, 179(6):1042-1046]

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EDUCATIONAL SERIES IN CONGENITAL HEART DISEASE: The sequential segmental approach to assessment.

Hannah Bellsham-Revell, Navroz Masani,

Sequential segmental analysis allows clear description of the cardiac structure in a logical fashion without assumptions and confusing nomenclature. Each segment is analysed, and then the connections described followed by any associated anomalies. For the echocardiographer there are several key features of the cardiac structures to help differentiate and accurately ... Read more >>

Echo Res Pract (Echo research and practice)
[2019, 6(1):R1-R8]

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Bidirectional flow across a perforate cor triatriatum dexter in a dog with concurrent pulmonary, tricuspid, and mitral valve dysplasia.

C M Hokanson, J D Rhinehart, B A Scansen,

A 10-week-old male intact mixed breed dog presented for evaluation of suspected right-sided congestive heart failure. Echocardiographic imaging revealed a perforate cor triatriatum dexter (CTD), along with pulmonary valve stenosis and tricuspid and mitral valve dysplasia. In typical CTD cases, there is unidirectional blood flow across the dividing membrane, from ... Read more >>

J Vet Cardiol (Journal of veterinary cardiology : the official journal of the European Society of Veterinary Cardiology)
[2019, 21:93-97]

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Leiomyoma development in Mayer-Rokitansky-Küster-Hauser syndrome: a case report and a narrative review of the literature.

Nikolaos Blontzos, Christos Iavazzo, George Vorgias, Nikolaos Kalinoglou,

The development of leiomyomas on the grounds of an aplastic/hypoplastic uterus in patients with Mayer-Rokitansky-Küster-Hauser syndrome (MRKHS) has been rarely described. We report the first case of development of multiple leiomyomas in a patient with MRKHS complicated with pulmonary valve stenosis, and we present a narrative review of the existing ... Read more >>

Obstet Gynecol Sci (Obstetrics & gynecology science)
[2019, 62(4):294-297]

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Rheumatic Fever in Large Cohort of Adolescents in Israel.

Yossy Machluf, Yoram Chaiter, Rivka Farkash, Anat Sebbag, Daniel Lyon Fink,

Background: Acute rheumatic fever (ARF) remains a major worldwide healthcare problem, despite its progressive decline in developed countries. The aims of our study were to estimate the prevalence of ARF among adolescents in Israel and to investigate risk factors. Methods: The study population consisted of 113,671 consecutive conscripts 16-19 years ... Read more >>

Front Med (Lausanne) (Frontiers in Medicine)
[2019, 6:328]

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Validity of Pulmonary Valve Z-Scores in Predicting Valve-Sparing Tetralogy Repairs-Systematic Review †.

Raina Sinha, Vasu Gooty, Subin Jang, Ali Dodge-Khatami, Jorge Salazar,

There is a lack of consensus regarding the preoperative pulmonary valve (PV) Z-score "cut-off" in tetralogy of Fallot (ToF) patients to attempt a successful valve sparing surgery (VSS). Therefore, the aim of this study was to review the available evidence regarding the association between preoperative PV Z-score and rate of ... Read more >>

Children (Basel) (Children)
[2019, 6(5):]

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Double whammy: A case of bilateral bicuspid arterial valves in transposition, with a review of the literature.

Pushpa Shivaram, Kavisha Shah, Amy Dossey, Brian Reemtsen, Robert H Anderson,

Bicuspidity of both the semilunar valves is rarely reported. We report the first ever case of bilateral bicuspid semilunar valves in a case of transposition. ... Read more >>

Ann Pediatr Cardiol (Annals of pediatric cardiology)
[2019, 12(1):56-59]

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Management of the Adult with Arterial Switch.

John P Breinholt, Sheba John,

Dextro-transposition of the great arteries (d-TGA) is a lethal congenital heart defect in which the great arteries-the pulmonary artery and aorta-are transposed to create ventriculoarterial discordance. Corrective surgical interventions have resulted in significant improvements in morbidity and mortality for this once-fatal congenital heart defect. The initial palliative surgery for d-TGA ... Read more >>

Methodist Debakey Cardiovasc J (Methodist DeBakey cardiovascular journal)
[2019, 15(2):133-137]

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Pregnancy outcomes among 31 patients with tetralogy of Fallot, a retrospective study.

Kana Wang, Junguo Xin, Xiaodong Wang, Haiyan Yu, Xinghui Liu,

BACKGROUND:Tetralogy of Fallot (TOF) is a severe type of congenital heart disease (CHD) and it confers substantial risk to mother and fetus for pregnant women. However, the outcome of pregnancy in women with TOF has not been well studied. METHODS:Women with TOF who have been seen and/or delivered at our ... Read more >>

BMC Pregnancy Childbirth (BMC pregnancy and childbirth)
[2019, 19(1):486]

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