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1.
Prog Pediatr Cardiol ; 65: 101516, 2022 Jun.
Article in English | MEDLINE | ID: mdl-35313700

ABSTRACT

Background: Due to the COVID-19 pandemic a novel disease has emerged, multisystem inflammatory syndrome in children (MIS-C). It presents post virally after a COVID-19 infection, and its clinical presentation and symptoms are very similar to Kawasaki Disease (KD). Aim of review: The objective of this review is to compare and contrast differences of Kawasaki Disease and MIS-C. Key scientific concepts of the review: Kawasaki Disease and MIS-C are very similar in clinical presentation and symptomatology. Understanding the diagnostic criteria is crucial to making an accurate diagnosis. Treatments in Kawasaki Disease are established, while in MIS-C treatment protocols are continuing to develop. Careful history taking and laboratory marker analysis should guide the clinician to accurate diagnosis.

2.
J Perinatol ; 38(5): 537-542, 2018 05.
Article in English | MEDLINE | ID: mdl-29453434

ABSTRACT

OBJECTIVE: The influence of post-ligation cardiac syndrome (PLCS), a complication of patent ductus arteriosus (PDA) ligations, on neonatal outcomes is unknown. The purpose of this study was to determine the risks of PLCS on severe pulmonary morbidity and severe retinopathy of prematurity (ROP). STUDY DESIGN: Retrospective cohort study of infants who underwent a PDA ligation between 2006 and 2015. Data were collected on patients with and without PLCS. The primary outcome was the difference in severe bronchopulmonary dysplasia (BPD) between groups. Secondary outcomes included discharge with home oxygen and severe ROP. RESULT: A total of 100 infants that underwent PDA ligation during the study period were included in the study; 31 (31%) neonates developed PLCS. In adjusted analysis, PLCS was associated with increased risk for severe BPD (RR 1.67, 95% CI: 1.15-2.42) and home oxygen therapy (RR: 1.47, 95% CI: 1.09-1.99) only. No association with severe ROP was seen (RR: 1.48; 95% CI: 0.87-2.52). CONCLUSION: PLCS is associated with severe neonatal pulmonary morbidity, but not with severe ROP. Further investigation is warranted to validate these results.


Subject(s)
Cardiac Surgical Procedures/adverse effects , Ductus Arteriosus, Patent/surgery , Perioperative Care/methods , Postoperative Complications/diagnosis , Female , Humans , Infant, Newborn , Infant, Premature , Ligation/adverse effects , Logistic Models , Male , Morbidity , Postoperative Complications/therapy , Retrospective Studies , Syndrome
3.
Catheter Cardiovasc Interv ; 90(2): 281-289, 2017 Aug 01.
Article in English | MEDLINE | ID: mdl-28805027

ABSTRACT

OBJECTIVES: To describe acute and mid-term results of hybrid perventricular device closure of muscular ventricular septal defects (mVSDs). BACKGROUND: Perventricular device closure of mVSDs can mitigate technical limitations of percutaneous closure and need for cardiopulmonary bypass or ventriculotomy with a surgical approach. METHODS: This is a multicenter retrospective cohort study of patients undergoing hybrid perventricular mVSD device closure from 1/2004 to 1/2014. Procedural details, adverse events, outcomes, and follow-up data were collected. Patients were divided into two groups: (1) simple (mVSD closure alone) and (2) complex (mVSD closure with concomitant cardiac surgery). RESULTS: Forty-seven patients (60% female) underwent perventricular mVSD device closure at a median age of 5.2 months (IQR 1.8-8.9) and weight of 5.1 kg (IQR 4.0-6.9). Procedural success was 91% [100% (n = 22) simple and 84% (n = 21/25) complex]. Adverse events occurred in 19% (9/47) [9% (2/22) simple and 28% (7/25) complex]. Hospital length of stay (LOS) was shorter in the simple vs. complex group (4 vs. 14 days, P < 0.01). At mid-term follow-up of 19.2 months (IQR 2.3-43) 90% of pts had complete mVSD closure; none developed late heart block, increased atrioventricular (AV) valve insufficiency or ventricular dysfunction. CONCLUSIONS: Perventricular device closure of simple mVSD was associated with a high rate of procedural success, few adverse events, and short hospital LOS. Procedural adverse events were associated with the presence of concomitant complex surgery. Residual mVSD, AV valve insufficiency, or ventricular dysfunction were uncommon at mid-term follow-up. © 2017 Wiley Periodicals, Inc.


Subject(s)
Cardiac Surgical Procedures , Heart Septal Defects, Ventricular/therapy , Percutaneous Coronary Intervention/instrumentation , Septal Occluder Device , Cardiac Surgical Procedures/adverse effects , Child , Child, Preschool , Echocardiography, Transesophageal , Female , Heart Septal Defects, Ventricular/diagnostic imaging , Humans , Infant , Length of Stay , Male , Percutaneous Coronary Intervention/adverse effects , Prosthesis Design , Retrospective Studies , Risk Factors , Time Factors , Treatment Outcome , United States
4.
Hosp Pediatr ; 6(4): 234-42, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26956424

ABSTRACT

OBJECTIVES: To evaluate a scheduled interprofessional huddle among pediatric residents, nursing staff, and cardiologists on the number of high-risk transfers to the ICU. METHODS: A daily, night-shift huddle intervention was initiated between the in-house pediatric residents and nursing staff covering the cardiology ward patients with the at-home attending cardiologist. Retrospective cohort chart review identified high-risk transfers from the inpatient floor to the ICU over a 24-month period (eg, inotropic support, intubation, and/or respiratory support within 1 hour of ICU transfer). Satisfaction with the intervention and the impact of the intervention on team-based communication and resident education was collected using a retrospective pre-post survey. RESULTS: Ninety-three patients were identified as unscheduled transfers from the ward team to the ICU. Overall, 21 preintervention transfers were considered high risk, whereas only 8 patients were considered high risk after the intervention (P=.004). During the night shift, high risk transfers decreased from 8 of 17 (47%) to 3 of 21 patients (14%) (P=.03). Interprofessional communication improved with 12 of 14 nurses and 24 of 25 residents reporting effective communication after the intervention (P<.0001) compared with only 1 nurse and 15 residents reporting a positive experience before the intervention. Overall, all 3 provider groups stated an improved experience covering a high-risk cardiology patient population. CONCLUSIONS: Implementation of an interprofessional huddle may contribute to decreasing high-risk transfers to the ICU. Initiating a daily huddle was well received and allowed for open lines of communication across all provider groups.


Subject(s)
Cardiology/methods , Interdisciplinary Communication , Internship and Residency , Nurses , Patient Transfer , Pediatrics , Attitude of Health Personnel , Female , Humans , Intensive Care Units/statistics & numerical data , Internship and Residency/methods , Internship and Residency/statistics & numerical data , Male , Nurses/psychology , Nurses/statistics & numerical data , Patient Transfer/methods , Patient Transfer/standards , Pediatrics/methods , Pediatrics/standards , Personnel Staffing and Scheduling/standards , Quality Improvement , Risk Adjustment
5.
Pediatr Cardiol ; 33(1): 109-14, 2012 Jan.
Article in English | MEDLINE | ID: mdl-21892648

ABSTRACT

This study sought to determine the safety and effectiveness of cryo-balloon angioplasty (CbA) for pulmonary vein stenosis (PVS) in pediatric patients. Current therapy options for PVS are less than satisfactory due to recurrent progressive restenosis and neointimal proliferation. Catheterization database, hospital records, imaging studies, and pathologic specimens were reviewed for procedural-related and outcomes data in all patients who underwent pulmonary vein (PV) CbA using the Boston Scientific PolarCath Peripheral Dilation System between August 2006 and June 2009. Thirteen patients (19 PVs; median age 13 months [range 3.5 months to 18.5 years] and weight 7.9 kg [range 3.8 to 47.7]) underwent CbA. Mean PVS diameter after CbA increased from 2.19 (± 0.6) to 3.77 (± 1.1) mm (p < 0.001). Mean gradient decreased from 14 (± 7.4) to 4.89 (± 3.2) mm Hg (p < 0.001). Mean stenosis-to-normal vein diameter ratio increased from 0.52 (± 0.15) to 0.89 (± 0.33) (p < 0.001). Eight patients underwent repeat catheterization a mean of 5.6 months (± 3.66) later. Improved PVS diameter was maintained in 2 PVs. Four veins had restenosis but maintained diameters greater than that before initial CbA. In 11 PVs, the diameter decreased from 4.28 (± 1.14) to 2.53 (± 0.9) mm (p = 0.001). Mean gradient increased from 3.55 (± 3.0) to 14.63 (± 9.6) mm Hg (p = 0.011). All vessels underwent repeat intervention with acute relief of PVS. Stroke occurred within 24 h of CbA in 1 patient. CbA of PVS is safe and results in acute relief of stenosis. However, CbA appears minimally effective as the sole therapy in maintaining long-term relief of PVS.


Subject(s)
Angioplasty, Balloon/methods , Cardiac Catheterization/methods , Cryotherapy/methods , Pulmonary Veno-Occlusive Disease/surgery , Adolescent , Angioplasty, Balloon/adverse effects , Cardiac Catheterization/adverse effects , Child , Child, Preschool , Cryotherapy/adverse effects , Female , Follow-Up Studies , Humans , Infant , Male , Retrospective Studies , Treatment Outcome
6.
Pediatr Nephrol ; 22(3): 448-50, 2007 Mar.
Article in English | MEDLINE | ID: mdl-17043882

ABSTRACT

Acute post-streptococcal glomerulonephritis (APSGN) is rare in children under 2 years of age. This is related in part to the disease patterns of group A streptococcus (GAS) and in part to impaired immunogenicity in infants. We report the case of a 14-month-old child with APSGN following GAS pharyngitis. This case illustrates that APSGN needs to be considered in the evaluation of both gross and microscopic hematuria in this age group. We review the literature of both GAS and APSGN and discuss the pathogenesis and epidemiologic reasons for this association.


Subject(s)
Glomerulonephritis/etiology , Pharyngitis/complications , Streptococcal Infections/complications , Streptococcus pyogenes , Acute Disease , Glomerulonephritis/diagnosis , Humans , Infant , Male
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