Results 61 to 70 of about 615,985 (187)

Genetic abnormalities/syndromes significantly impact perioperative outcomes of conotruncal heart defects

Annals of Pediatric Cardiology, 2020
Objectives : The main objective of the study is to characterize the effects of genetic abnormalities/syndromes (GA/S) on perioperative outcomes of cardiac surgeries involving repair of conotruncal heart defects (CTHD).
Subhrajit Lahiri, Wernovsky Gil, Salyakina Daria, Gruber Joshua, Jayakar Parul, Burke Redmond, Welch Elizabeth   +6 more
doaj   +1 more source

Congenital Intraoral Synechiae: A Scoping Review of Airway, Feeding, and Surgical Management

Otolaryngology–Head and Neck Surgery, EarlyView.
Abstract Objective To map the existing literature on congenital intraoral synechiae and summarize reported anatomic patterns, clinical presentation, associated anomalies/syndromes, and outcomes to inform standardized diagnostic and therapeutic approaches. Data Sources PubMed, CINAHL, Embase, Web of Science, and Google Scholar were searched from January
Jason Bernier, Mathieu Bergeron
wiley   +1 more source

Case report: Diagnosis of a double aortic arch in the primary care setting

Journal of Family Medicine and Primary Care
A double aortic arch is a rare congenital heart anomaly not typically diagnosed in adults. It can present with nonspecific symptoms including dysphagia, a cough, and hoarseness which can lead to a delay in diagnosis or misdiagnosis.
Mary Chick
doaj   +1 more source

Diagnostic Yield of Post‐Mortem Fetal Micro‐CT for Thoracic Abnormalities

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective This study aims to identify the imaging findings specifically for thoracic anomalies in 1200 Micro‐CT cases, independent of whether the abnormality contributed to the main diagnosis or cause of death. Method We analyzed 1200 Micro‐CT scans in an unselected, consecutive cohort between 2017 and 2024 to identify thoracic anomalies ...
Ian C. Simcock, Audrey Lamouroux, Susan C. Shelmerdine, J. Ciaran Hutchinson, Neil J. Sebire, Owen J. Arthurs   +5 more
wiley   +1 more source

Acute aortic syndromes

, 2014
Acute aortic syndromes comprise acute aortic dissection, intramural haematoma, symptomatic penetrating aortic ulcers and traumatic aortic dissection. These conditions result primarily from disruption of the outer aortic layer, and involve thinning of the
Clough, Rachel; id_orcid, Nienaber, Christoph A., Akin, Ibrahim, Rehders, Tim C.   +3 more
core   +1 more source

Transplacental Flecainide and/or Digoxin for Fetal Tachyarrhythmias: Therapeutic Efficacy and Clinical Experience

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective To assess the efficacy and safety of transplacental flecainide and/or digoxin for fetal tachyarrhythmias when sotalol is unavailable. Method We evaluated transplacental flecainide, digoxin, or combination therapy in a retrospective and prospective cohort across two Thai tertiary centers.
Mukpradab Darakamas, Sanitra Anuwutnavin, Fuanglada Tongprasert, Wisit Chankhunaphas, Kanyarat Nilto, Supaluck Kanjanauthai, Jarupim Soongswang   +6 more
wiley   +1 more source

Еndovascular treatment of traumatic aortic injury [PDF]

Българска кардиология
Acute aortic syndromes represent a group of life-threatening conditions characterized by disruption of the integrity of the aortic wall and a high risk of rupture and fatal outcome.
P. Simeonov, I. Dimitrova, B. Barzashka, V. Grudeva   +3 more
doaj   +3 more sources

Clinical Outcomes and Acute Exacerbation Incidence in Combined Pulmonary Fibrosis and Emphysema

Respirology, EarlyView.
This multicentre prospective study of 1016 patients demonstrated that CPFE, defined as ≥ 5% emphysema on visual CT assessment, identified a high‐risk phenotype with significantly worse 5‐year survival compared to non‐CPFE IIP patients (51.4% vs. 63.1%) and COPD patients (51.4% vs. 84.0%) and higher acute exacerbation incidence, validating international
Kazuya Tsubouchi, Yasuaki Kotetsu, Tomotsugu Takano, Hiroaki Ogata, Fumiaki Kiyomi, Katsuyuki Ichiki, Shohei Takata, Yasuhiko Kitasato, Hiroshi Ishii, Kazuhiro Yatera, Kei Yamasaki, Masaki Okamoto, Makoto Yoshida, Masayuki Kawasaki, Masaki Fujita, Tomohiro Ogawa, Kazunori Tobino, Eiji Harada, Noriaki Nakagaki, Masashi Komori, Taishi Harada, Hiroshi Wataya, Yoichi Nakanishi, Isamu Okamoto   +23 more
wiley   +1 more source

Persistent Fifth Aortic Arch Associated with 22q11.2 Deletion Syndrome

, 2008
Background: Chromosome 22q 11.2 deletion is frequently associated with conotruncal malformations and aortic arch anomalies. This study investigated the association of chromosome 22q 11.2 deletion with clinical manifestations in four pediatric patients ...
李孟倫;陳曉能;陳明;曹龍彥;王寶田;李美慧;邱英世, LEE, MENG-LUEN;CHEN, HSIAO-NENG;CHEN, MING;TSAO, LON-YEN;WANG, BAO-TYAN;LEE, MEI-HUI;CHIU, ING-SH   +1 more
core  

Hybrid repair of an aortic arch aneurysm with complex anatomy: Right aortic arch and anomalous origin of supra-aortic vessels

, 2007
We performed a one-stage hybrid surgical and endovascular procedure to manage a 6.5-cm right aortic arch aneurysm associated with anomalous origin of the supra-aortic vessels in a 70-year-old man.
Roberto Chiesa, Germano Melissano, Fabio Calliari, Luca Bertoglio, Bertoglio L, CHIESA , ROBERTO, Calliari F., MELISSANO , GERMANO   +7 more
core   +2 more sources