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119


One Size Does Not Fit All: The Story of Pediatric Ventricular Assist Devices!

Kumar, T K Susheel; Paone, Darien
PMID: 37673313
ISSN: 1552-6259
CID: 5689462

Medical Management of Canine Chronic Ulcerative Stomatitis Using Cyclosporine and Metronidazole

Ford, Kimberly R; Anderson, Jamie G; Stapleton, Barbara L; Murphy, Brian G; Kumar, T K Santosh; Archer, Todd; Mackin, Andrew J; Wills, Robert W
Canine chronic ulcerative stomatitis (CCUS) is a spontaneously occurring, painful, and often debilitating condition of the oral cavity, with a suspected immune-mediated component. The response to pharmacological treatment is generally poor, thus the need to identify more effective medical therapies for this condition. This article describes a prospective clinical trial that was designed to evaluate the efficiency of a combination of cyclosporine and metronidazole in managing CCUS. The hypothesis was that a combination of cyclosporine and metronidazole would effectively minimize clinical signs associated with CCUS. Ten client-owned dogs with a biopsy-confirmed diagnosis consistent with CCUS were prescribed cyclosporine (5 mg/kg) for 1 week, followed by the addition of metronidazole (15-20 mg/kg), both administered orally once daily. The cyclosporine dosage interval was lengthened over time. Dogs were observed for a 6-month period and evaluated using a 32-point Canine Ulcerative Stomatitis Disease Activity Index (CUSDAI). Regular cyclosporine therapeutic drug monitoring was also conducted by the measurement of whole blood cyclosporine levels and the pharmacodynamic assessment of the T-cell expression of IL-2. The results demonstrated that a combination of cyclosporine and metronidazole was effective in minimizing the clinical signs of CCUS and in reducing CUSDAI scores. Neither blood cyclosporine levels nor the T-cell expression of IL-2 predicted improvement in clinical signs and CUSDAI scores, although there was a correlation between blood drug concentrations and the suppression of T-cell IL-2 expression. The evaluation of clinical signs and CUSDAI scores appears to be the most effective means of assessing response to therapy, and therapeutic drug level monitoring does not appear to be routinely indicated.
PMID: 36650996
ISSN: 2470-4083
CID: 5689432

Chronic Medication Burden After Cardiac Surgery for Pediatric Medicaid Beneficiaries

Woo, Joyce L; Nash, Katherine A; Dragan, Kacie; Crook, Sarah; Neidell, Matthew; Cook, Stephen; Hannan, Edward L; Jacobs, Marshall; Goldstone, Andrew B; Petit, Christopher J; Vincent, Robert; Walsh-Spoonhower, Kathleen; Mosca, Ralph; Kumar, T K Susheel; Devejian, Neil; Kamenir, Steven A; Alfieris, George M; Swartz, Michael F; Meyer, David; Paul, Erin A; Newburger, Jane W; Billings, John; Davis, Matthew M; Anderson, Brett R; ,
BACKGROUND:Congenital heart defects are the most common and resource-intensive birth defects. As children with congenital heart defects increasingly survive beyond early childhood, it is imperative to understand longitudinal disease burden. OBJECTIVES:The purpose of this study was to examine chronic outpatient prescription medication use and expenditures for New York State pediatric Medicaid enrollees, comparing children who undergo cardiac surgery (cardiac enrollees) and the general pediatric population. METHODS:This was a retrospective cohort study of all Medicaid enrollees age <18 years using the New York State Congenital Heart Surgery Collaborative for Longitudinal Outcomes and Utilization of Resources database (2006-2019). Primary outcomes were total chronic medications per person-year, enrollees per 100 person-years using ≥1 and ≥3 medications, and medication expenditures per person-year. We described and compared outcomes between cardiac enrollees and the general pediatric population. Among cardiac enrollees, multivariable regression examined associations between outcomes and clinical characteristics. RESULTS:We included 5,459 unique children (32,131 person-years) who underwent cardiac surgery and 4.5 million children (22 million person-years) who did not. More than 4 in 10 children who underwent cardiac surgery used ≥1 chronic medication compared with approximately 1 in 10 children who did not have cardiac surgery. Medication expenditures were 10 times higher per person-year for cardiac compared with noncardiac enrollees. Among cardiac enrollees, disease severity was associated with chronic medication use; use was highest among infants; however, nearly one-half of adolescents used ≥1 chronic medication. CONCLUSIONS:Children who undergo cardiac surgery experience high medication burden that persists throughout childhood. Understanding chronic medication use can inform clinicians (both pediatricians and subspecialists) and policymakers, and ultimately the value of care for this medically complex population.
PMID: 37730290
ISSN: 1558-3597
CID: 5689472

AI-driven quantification of ground glass opacities in lungs of COVID-19 patients using 3D computed tomography imaging

Saha, Monjoy; Amin, Sagar B; Sharma, Ashish; Kumar, T K Satish; Kalia, Rajiv K
OBJECTIVES:Ground-glass opacity (GGO)-a hazy, gray appearing density on computed tomography (CT) of lungs-is one of the hallmark features of SARS-CoV-2 in COVID-19 patients. This AI-driven study is focused on segmentation, morphology, and distribution patterns of GGOs. METHOD:We use an AI-driven unsupervised machine learning approach called PointNet++ to detect and quantify GGOs in CT scans of COVID-19 patients and to assess the severity of the disease. We have conducted our study on the "MosMedData", which contains CT lung scans of 1110 patients with or without COVID-19 infections. We quantify the morphologies of GGOs using Minkowski tensors and compute the abnormality score of individual regions of segmented lung and GGOs. RESULTS:PointNet++ detects GGOs with the highest evaluation accuracy (98%), average class accuracy (95%), and intersection over union (92%) using only a fraction of 3D data. On average, the shapes of GGOs in the COVID-19 datasets deviate from sphericity by 15% and anisotropies in GGOs are dominated by dipole and hexapole components. These anisotropies may help to quantitatively delineate GGOs of COVID-19 from other lung diseases. CONCLUSION:The PointNet++ and the Minkowski tensor based morphological approach together with abnormality analysis will provide radiologists and clinicians with a valuable set of tools when interpreting CT lung scans of COVID-19 patients. Implementation would be particularly useful in countries severely devastated by COVID-19 such as India, where the number of cases has outstripped available resources creating delays or even breakdowns in patient care. This AI-driven approach synthesizes both the unique GGO distribution pattern and severity of the disease to allow for more efficient diagnosis, triaging and conservation of limited resources.
PMID: 35286309
ISSN: 1932-6203
CID: 5689412

Giant mediastinal teratoma in a young infant: a case report [Case Report]

Howell, Raelina S; Magid, Margret S; Kuenzler, Keith A; Kumar, T K Susheel
Background/UNASSIGNED:Giant mediastinal tumors in the pediatric population can pose unique challenges for resection such as cardiovascular collapse on induction of anesthesia and injury to surrounding structures that may be compressed, displaced, or invaded by the mass. Principles that must be borne in mind during removal of giant mediastinal masses include: appropriate cross-sectional imaging to define extent of mass; airway control during induction of anesthesia; a multidisciplinary collaborative approach including cardiothoracic surgery; preparation for urgent sternotomy; plan for peripheral cannulation to institute cardiopulmonary bypass if needed; preservation of neurovasculature structures during dissection; complete resection whenever possible. While complete resection is desirable and results in an excellent prognosis, it may not be achievable especially if the tumor encases coronary arteries, and it is acceptable to leave small amounts of tumor behind. Case Description/UNASSIGNED:Here we present a case describing surgical management of a giant mediastinal teratoma in a two-month-old female. The patient was found to have a large mediastinal mass during workup for cough and noisy breathing. She underwent preoperative echocardiogram demonstrating normal cardiac function followed by uncomplicated, open resection of the mass. Conclusions/UNASSIGNED:Giant mediastinal tumors give rise to unique challenges for resection in small infants. The principles of airway control, preparation for urgent sternotomy, preparation for peripheral cardiopulmonary bypass cannulation, and preservation of neurovasculature during dissection must be borne in mind.
PMCID:9385876
PMID: 36164358
ISSN: 2522-6711
CID: 5334112

Biatrial drainage of right superior vena cava with left superior vena cava: A diagnostic conundrum [Case Report]

Bhansali, Suneet; Cohen, Roi B; Halpern, Dan; Saharan, Sunil; Saric, Muhamed; Kumar, T K Susheel; Mosca, Ralph S
PMCID:9366530
PMID: 35967232
ISSN: 2666-2507
CID: 5299732

Norwood modification for hypoplastic left heart and right aortic arch [Case Report]

Kumar, T K Susheel; Williams, David; Scheinerman, Joshua; Bhansali, Suneet; Ramirez, Michelle; Chakravarti, Sujata; Crawford, Maya; Mosca, Ralph
PMCID:9196980
PMID: 35711181
ISSN: 2666-2507
CID: 5282772

Elevated Levels of Urinary Biomarkers TIMP-2 and IGFBP-7 Predict Acute Kidney Injury in Neonates after Congenital Heart Surgery

Ramírez, Michelle; Chakravarti, Sujata; Busovsky-McNeal, Melissa; McKinstry, Jaclyn; Al-Qaqaa, Yasir; Sahulee, Raj; Kumar, T K Susheel; Li, Xiaochun; Goldberg, Judith D; Gefen, Ashley M; Malaga-Dieguez, Laura
PMCID:9208843
PMID: 35734207
ISSN: 2146-4618
CID: 5282022

Aortic migration of Amplatzer Piccolo (TM) ductal Occluder

Minocha, Prashant K.; Sutton, Nicole; Crawford, Maya T.; Williams, David; Ramirez, Michelle; Chakravarti, Sujata; Mosca, Ralph; Kumar, T. K. Susheel
ISI:000760926200001
ISSN: 1047-9511
CID: 5243012

Tricuspid atresia with absent pulmonary valve: A rare form of single ventricle

Naik, Ronak; Makadia, Luv D; Ramirez, Michelle; Crawford, Maya T; Ahmad, Latifah; Kumar, T K Susheel
Tricuspid atresia with an absent pulmonary valve is a rare congenital cardiac defect. Although extensive pathological reviews have been published in the past, there are only a handful of cases that have been successfully palliated to the stage of Fontan. We hereby describe the successful management of one such case and review the surgical strategies described in the literature.
PMID: 35434814
ISSN: 1540-8191
CID: 5232782