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Cetta, Frank

0009-0006-7987-502X

Mayo Clinic

Mayo Clinic

Citations 63

Prevalence of pulmonary hypertension in adults after atrial switch and role of ventricular filling pressures
Miranda, William R. , Jain, C. Charles , Connolly, Heidi M. , Cetta, Frank , Egbe, Alexander C. , Hagler, Donald J. , DuBrock, Hilary M.

Heart | October 7, 2020 | Volume: 107 | Issue: 6 | Pages: 468-473

10.1136/heartjnl-2020-317111 Get It

Objective To assess the prevalence of elevated systemic right ventricular (sRV) end-diastolic pressure and pulmonary arterial hypertension in adults with transposition of the great arteries (TGA) who have undergone atrial switch operation. Methods Forty-two adults (aged ≥18 years) with complete TGA and atrial switch palliation undergoing cardiac catheterisation between 2004 and 2018 at Mayo Clinic, MN, were identified. Clinical, echocardiographic and invasive haemodynamic data were abstracted from the medical charts and procedure logs. Results Mean age was 37.6±7.9 years; 28 were male (67%). The Mustard operation was performed in 91% of individuals. Mean estimated sRV ejection fraction by echocardiography was 33.3%±10.9% and ≥moderate tricuspid (systemic atrioventricular valve) regurgitation was present in 15 patients (36%). Mean sRV end-diastolic pressure was 13.2±5.4 mm Hg. An sRV end-diastolic pressure >15 mm Hg was present in 35% of individuals whereas a pulmonary artery wedge pressure (PAWP) >15 mm Hg was seen in 59%. Mean pulmonary artery pressure ≥25 mm Hg was seen in 47.5% of patients with PAWP being >15 mm Hg in all but one patient. Conclusion In adults after atrial switch, elevated sRV end-diastolic pressure was present in only one-third of patients whereas increased PAWP was seen in almost 60%. These findings are most likely related to a combination of decreased pulmonary atrial (functional left atrium) compliance and, in a subset of patients, pulmonary venous baffle obstruction. Elevation in pulmonary pressures was highly prevalent with concomitant elevation in PAWP being present in essentially all patients.
Surgical Management of Right Aortic Arch Obstruction Associated With Rare Form of Vascular Ring
Cetta, Frank , Egunov, O.A. , Sviazov, Evgenii A. , Киселев, В. О. , Troshkinev, Nikita M. , Egunov, Oleg A , Кривощеков, Е. В.

World Journal for Pediatric and Congenital Heart Surgery | February 25, 2020 | Volume: 11 | Issue: 2 | Pages: 222-225

10.1177/2150135119885893 Get It

This clinical case demonstrated surgical management for a rare case of vascular ring associated with an elongated and kinked aortic arch and a right descending aorta in a ten-year-old male using an extra-anatomic bypass grafting method and dividing the vascular ring. Computer tomography performed at six-month follow-up showed a favorable surgical outcome.
Hypoplastic Left Heart Syndrome: An Overview for Primary Care Providers
Javed, Rabia, Cetta, Frank , Said, Sameh M. , Olson, Timothy M. , Qureshi, M. Yasir , Qureshi, Muhammad Y , Olson, Timothy M , O’Leary, Patrick

Pediatrics In Review | July 1, 2019 | Volume: 40 | Issue: 7 | Pages: 344-353

10.1542/pir.2018-0005 Get It

Hypoplastic left heart syndrome is one of the most complex congenital heart diseases and requires several cardiac surgeries for survival. The diagnosis is usually established prenatally or shortly after birth. Each stage of surgery poses a unique hemodynamic situation that requires deeper understanding to manage common pediatric problems such as dehydration and respiratory infections. Careful multidisciplinary involvement in the care of these complex patients is improving their outcome; however, morbidity and mortality are still substantial. In this review, we focus on the hemodynamic aspects of various surgical stages that a primary care provider should know to manage these challenging patients.
Fate of the Fontan connection: Mechanisms of stenosis and management
Hagler, Donald J. , Miranda, William R. , Haggerty, Brielle J., Johnson, Jonathan N. , Cetta, Frank , Said, Sameh M. , Taggart, Nathaniel W. , Anderson, Jason H. , Johnson, Jonathan , Taggart, Nathaniel W

Congenital Heart Disease | February 26, 2019 | Volume: 14 | Issue: 4 | Pages: 571-581

10.1111/chd.12757 Get It

What is the role of apical ventriculotomy in children and young adults with hypertrophic cardiomyopathy?
Thompson, Alex , Dearani, Joseph A. , Johnson, Jonathan N. , Schaff, Hartzell V. , Towe, Eric, Palfreeman, Jared, Wackel, Philip L. , Cetta, Frank , Thompson, Alex J , Towe, Eric C, Schaff, Hartzell , Dearani, Joseph A.

Congenital Heart Disease | July 19, 2018 | Volume: 13 | Issue: 4 | Pages: 617-623

10.1111/chd.12618 Get It

Repair of Sinus Venosus Defect and Anomalous Pulmonary Veins Associated With Vein of Galen Malformation
Anderson, Heather N., Said, Sameh M. , Cetta, Frank

World Journal for Pediatric and Congenital Heart Surgery | May 24, 2018 | Volume: 11 | Issue: 4 | Pages: NP151-NP154

10.1177/2150135118769325 Get It

Sinus venosus defect (SVD) is a deficiency in the sinus venosus portion of the atrium, often associated with partial anomalous pulmonary venous connections. In patients with vein of Galen malformation (VGAM), SVD provides a unique challenge with respect to embolization treatment. In our case, the child had percutaneous device closure of the SVD prior to VGAM embolization. Nine years later, he required surgical removal of the SVD device and Warden procedure due to progressive right-sided cardiac enlargement.
Arrhythmia after cone repair for Ebstein anomaly: The Mayo Clinic experience in 143 young patients
Wackel, Philip L. , Cannon, Bryan C. , Dearani, Joseph A. , Sessions, Kristen L., Holst, Kimberly , Johnson, Jonathan N. , Cetta, Frank , Wackel, Philip , Cannon, Bryan, Dearani, Joseph, Sessions, Kristen, Johnson, Jonathan , Dearani, Joseph A.

Congenital Heart Disease | January 10, 2018 | Volume: 13 | Issue: 1 | Pages: 26-30

10.1111/chd.12566 Get It

Lambl's excrescences in children: Improved detection via transthoracic echocardiography
Phillips, Amanda L., Qureshi, M. Yasir , Eidem, Benjamin W., Cetta, Frank , Qureshi, Muhammad Y

Congenital Heart Disease | November 28, 2017 | Volume: 13 | Issue: 2 | Pages: 251-253

10.1111/chd.12560 Get It

Ultrasound guided percutaneous common carotid artery access in piglets for intracoronary stem cell infusion
Taggart, Nathaniel W. , Edgerton, Sarah, Peral, Susana Cantero, Holst, Kimberly , Cetta, Frank , Anderson, Jason H. , Edgerton, Sarah L, Cantero Peral, Susana, Holst, Kimberly A, Taggart, Nathaniel W

Laboratory Animals | July 20, 2017 | Volume: 52 | Issue: 1 | Pages: 88-92

10.1177/0023677217719923 Get It

In pigs, the deep location of the common carotid artery and overlying sternomastoideus muscle in the neck has led to the recommendation for a surgical cutdown for common carotid access, as opposed to minimally invasive techniques for vascular access. We sought to determine if direct percutaneous common carotid artery access in piglets is attainable. Seventeen piglets were anesthetized and intubated. Under two-dimensional and color flow Doppler ultrasound guidance, a 21 gauge needle was utilized to access the right common carotid artery. Following arterial puncture, the Seldinger technique was applied to place a 4 or 5 French introducer. Upon completion of cardiac catheterization with intracoronary stem cell infusion the introducer was removed and manual pressure was applied to prevent hematoma development. Successful access with an introducer was achieved in all 17 piglets. The average weight was 8.5 ± 1.7 kg. One piglet developed a hematoma with hemorrhaging from the catheterization site and was euthanized. This piglet was given bivalirudin for the procedure. After this incident, subsequent piglets were not given anticoagulation and no other complications occurred. Ultrasound guided percutaneous common carotid artery access in piglets is attainable in a safe, reliable, and reproducible manner when performed by microvascular experts.
Surveillance for liver complications after the Fontan procedure
Hilscher, Moira , Johnson, Jonathan N. , Cetta, Frank , Driscoll, David J. , Poterucha, John J., Sánchez, William , Connolly, Heidi M. , Kamath, Patrick S. , Hilscher, Moira B, Sanchez, William

Congenital Heart Disease | January 31, 2017 | Volume: 12 | Issue: 2 | Pages: 124-132

10.1111/chd.12446 Get It