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Medical Policy
bmchp.org | 888-566-0008 wellsense.org | 877-957-1300 Medical Policy Ambulatory Cardiac Monitors (Excluding Holter Monitors) Policy Number: OCA 3.35 Version Number: 24 Version Effective Date: 03/01/21 + Product Applicability All Plan Products Well Sense Health Plan Boston Medical Center HealthNet Plan Well Sense Health Plan MassHealth Qualified Health Plans/ConnectorCare/Employer Choice Direct Senior Care Options ◊ Notes: + Disclaimer and audit information is located at the end of this document. ◊ The guidelines included in this Plan policy are applicable to members enrolled in Senior Care Options only if there are no criteria established for the specified service in a Centers for Medicare & Medicaid Services (CMS) national coverage determination (NCD) or local coverage determination (LCD) on the date of the prior authorization request. Review the member’s product-specific benefit documents at www.SeniorsGetMore.org to determine coverage guidelines for Senior Care Options. Policy Summary The Plan considers the use of ambulatory cardiac monitors in the outpatient setting to be medically necessary if the type of ambulatory cardiac monitor is covered for the Plan member and ALL applicable Plan criteria are met, as specified in the Medial Policy Statement and Limitations sections of this policy. Plan prior authorization is required. When the device is covered for the member, medically necessary ambulatory cardiac monitors utilized in the outpatient setting may include ambulatory cardiac event monitors, mobile cardiac outpatient telemetry, and/or single-use external ambulatory electrocardiographic monitoring patches available by prescription. Ambulatory Cardiac Monitors (Excluding Holter Monitors) + Plan refers to Boston Medical Center Health Plan, Inc. and its affiliates and subsidiaries offering health coverage plans to enrolled members. -
Surgeries by STAT Category
STAT SURGICAL PROCEDURE CATEGORY ASD repair, Patch 1 AVC (AVSD) repair, Partial (Incomplete) (PAVSD) 1 PFO, Primary closure 1 ASD repair, Primary closure 1 VSD repair, Patch 1 DCRV repair 1 Aortic stenosis, Subvalvar, Repair 1 Coarctation repair, End to end 1 Vascular ring repair 1 ICD (AICD) implantation 1 ICD (AICD) ([automatic] implantable cardioverter deFibrillator) procedure 1 ASD Repair, Patch + PAPCV Repair 1 VSD repair, Primary closure 1 AVC (AVSD) repair, Intermediate (Transitional) 1 PAPVC repair 1 TOF repair, No ventriculotomy 1 TOF repair, Ventriculotomy, Nontransanular patch 1 Conduit reoperation 1 Valve replacement, Pulmonic (PVR) 1 Valve replacement, Aortic (AVR), Mechanical 1 Valve replacement, Aortic (AVR), Bioprosthetic 1 Sinus oF Valsalva, Aneurysm repair 1 Fontan, TCPC, Lateral tunnel, Fenestrated 1 Coarctation repair, Interposition graFt 1 Pacemaker procedure 1 Glenn (Unidirectional cavopulmonary anastomosis) (Unidirectional Glenn) 1 PAPVC Repair, BaFFle redirection to leFt atrium with systemic vein translocation (Warden) (SVC 1 sewn to right atrial appendage) 1 1/2 ventricular repair 2 PA, Reconstruction (Plasty), Main (Trunk) 2 Valvuloplasty, Aortic 2 Ross procedure 2 LV to aorta tunnel repair 2 Valvuloplasty, Mitral 2 Fontan, Atrio-pulmonary connection 2 PDA closure, Surgical 2 Aortopexy 2 Pacemaker implantation, Permanent 2 Arrhythmia surgery - ventricular, Surgical Ablation 2 Bilateral bidirectional cavopulmonary anastomosis (BBDCPA) (Bilateral bidirectional Glenn) 2 Superior Cavopulmonary anastomosis(es) + PA -
Interstage Monitoring for the Infant with Hypoplastic Left Heart Syndrome What the Direct Care Nurse Needs to Know Jennifer Stra
Interstage Monitoring for the Infant with Hypoplastic Left Heart Syndrome What the Direct Care Nurse Needs to Know Jennifer Strawn, BSN, RN, CPN, Children’s Hospital & Medical Center, Omaha, Nebraska Jo Ann Nieves MSN, CPN, ARNP, PNP-BC, FAHA, Miami Children’s Hospital Bronwyn Bartle, DNP, CPNP-AC/PC, Duke Children’s Pediatric and Congenital Heart Center Mary Rummell, MN, RN, CNS, CPNP, FAHA, Oregon Health and Science University Introduction: Children born with hypoplastic left heart syndrome (HLHS) are at high risk for serious morbidity, growth failure and mortality during the time from discharge home after first stage HLHS palliation, until admission for the second stage surgical intervention. To improve outcomes and survival during this time, referred to as the “interstage period”, multiple strategies have been successfully implemented resulting in improved interstage survival. A critical element of interstage care is family education and training. Variations in practice and interstage home surveillance do exist but general guidelines are described below. Definitions: Possible newborn interventions for HLHS Figure 1: First stage surgical palliation procedures for hyoplastic left heart syndrome A. Norwood Procedure B. Norwood Procedure with C. Hybrid Stage I with BT shunt RV to PA shunt (“Sano”) Procedure Surgical: Norwood /Modified Blalock Taussig (BT) shunt procedure – the Norwood aortic reconstruction of the ascending aorta and arch consists of enlarging the ascending aorta by using part of the proximal native main pulmonary artery (PA) with other material (Gore-Tex or homograft material) to connect the PA to the aorta. Pulmonary blood flow is provided by a controlled shunt (BT shunt) usually made from Gore-Tex and connects the right subclavian artery to the right pulmonary artery. -
Long Term Consequences of the Fontan Procedure and How to Manage Them
ACCEPTED MANUSCRIPT Long Term Consequences of the Fontan Procedure and How to Manage Them Authors: W. Aaron Kay, MD1 Tabitha Moe, MD2 Blair Suter, MD3 Andrea Tennancour, NP1 Alice Chan, NP4 Richard A. Krasuski, MD5 Ali N. Zaidi, MD4 1. Indiana University School of Medicine, Krannert Institute of Cardiology, IN 2. University of Arizona School of Medicine, Phoenix, AZ 3. Indiana University School of Medicine, Departments of Medicine and Pediatrics, IN 4. Children’s Hospital at Montefiore, Montefiore Medical Center, Albert Einstein College of Medicine, NY 5. Duke University Health System, Durham, NC *Address reprint requests to: W. Aaron Kay, MD. 1801 N. Senate Blvd Suite 2000, Indianapolis IN. Email: [email protected] Emails of additional authors: Moe TG: [email protected] Suter BC: [email protected] Tennancour AE: [email protected] Chan A: [email protected] Krasuski RA: [email protected] Zaidi AN: [email protected] Disclosures: W. Aaron Kay: Nothing to disclose Tabitha Moe: Nothing to disclose Blair Suter, MD: Nothing to disclose Andrea Tennancour, NP: Nothing to disclose Alice Chan, NP: Nothing to disclose Ali N. Zaidi, MD: Nothing to disclose Richard A. Krasuski, MD: Dr. Krasuski serves a consultant and receives research funding from Actelion Pharmaceuticals.ACCEPTED He also serves as anMANUSCRIPT investigator for Edwards Lifesciences and is an unpaid member of the scientific advisory board for Ventripoint. ___________________________________________________________________ This is the author's manuscript of the article published in final edited form as: Kay, W. A., Moe, T., Suter, B., Tennancour, A., Chan, A., Krasuski, R. A., & Zaidi, A. N. (2018). Long Term Consequences of the Fontan Procedure and How to Manage Them. -
Comparison of Hybrid and Norwood Strategies in Hypoplastic Left Heart Syndrome
SURGERY | REVIEW Comparison of Hybrid and Norwood Strategies in Hypoplastic Left Heart Syndrome Hideyuki Kato, MD, Osami Honjo, MD, PhD, Glen Van Arsdell, MD, Christopher A. Caldarone, MD Division of Cardiovascular Surgery, Hospital for Sick Children, Labatt Family Heart Center Received 12/12/2011, Reviewed 27/12/2011, Accepted 1/1/2012 Key words: Hybrid strategy, Norwood strategy, single ventricle, hypoplastic left heart syndrome DOI: 10.5083/ejcm.20424884.70 ABSTRACT CORRESPONDENCE Current surgical palliation for neonates with single ventricle physiology includes Norwood-based Christopher A. Caldarone, MD, and Hybrid-based surgical strategies. When transplantation is not available, clinicians must choose Professor and Chair, Division of Cardiac Surgery, between these two strategies with distinctly different learning curves and risk profiles. The Norwood University of Toronto, strategy has evolved over several decades while the rising popularity of the Hybrid strategy is a Watson Family Chair in much more recent addition to our therapeutic options. Based upon the premise that avoiding cardio Cardiovascular Science – pulmonary bypass in the neonatal period and deferral of aortic arch reconstruction until a second Labatt Family Heart Center, stage procedure have an important influence on outcomes, the Hybrid strategy has compelling Hospital for Sick Children, theoretical advantages and disadvantages in comparison to the Norwood strategy. The purpose 555 University Avenue, of this review is to summarise the currently available data to support -
Risk Factors for Mortality After the Norwood Procedureq
European Journal of Cardio-thoracic Surgery 22 (2002) 82–89 www.elsevier.com/locate/ejcts Risk factors for mortality after the Norwood procedureq J. William Gaynora,*, William T. Mahleb, Mitchell I. Cohenb, Richard F. Ittenbachc, William M. DeCamplia, James M. Stevend, Susan C. Nicolsond, Thomas L. Spraya Downloaded from https://academic.oup.com/ejcts/article/22/1/82/516394 by guest on 28 September 2021 aDivision of Cardiothoracic Surgery, The Cardiac Center at The Children’s Hospital of Philadelphia, 34th Street and Civic Center Boulevard, Suite 8527, Philadelphia, PA 19104, USA bDivision of Cardiology, The Cardiac Center at The Children’s Hospital of Philadelphia, Philadelphia, PA, USA cDivision of Biostatistics and Epidemiology, The Cardiac Center at The Children’s Hospital of Philadelphia, Philadelphia, PA, USA dDivision of Cardiac Anesthesiology, The Cardiac Center at The Children’s Hospital of Philadelphia, Philadelphia, PA, USA Received 18 September 2001; received in revised form 7 March 2002; accepted 22 March 2002 Abstract Objectives: Recent studies have suggested that survival following the Norwood procedure is influenced by anatomy and is worse for patients with hypoplastic left heart syndrome (HLHS), particularly aortic atresia (AA), as compared to other forms of functional single ventricle and systemic outflow tract obstruction. The current study was undertaken to evaluate our recent experience with the Norwood procedure and to evaluate potential predictors of operative and 1-year mortality. Methods: A retrospective study of risk factors for operative and 1-year mortality in 158 patients undergoing the Norwood procedure between January 1, 1998 and June 30, 2001. Results: HLHS was present in 102 patients (70 with AA) and other forms of functional single ventricle with systemic outflow tract obstruction in the remaining 56. -
The Intensive Care of Infants with Hypoplastic Left Heart Syndrome
F97 Arch Dis Child Fetal Neonatal Ed: first published as 10.1136/adc.2004.064337 on 21 February 2005. Downloaded from RECENT ADVANCES The intensive care of infants with hypoplastic left heart syndrome U Theilen, L Shekerdemian ............................................................................................................................... Arch Dis Child Fetal Neonatal Ed 2005;90:F97–F102. doi: 10.1136/adc.2004.051276 Until a little over two decades ago, hypoplastic left heart excessive pulmonary blood flow, an important subgroup may have inadequate inter-atrial mix- syndrome was considered an inoperable and fatal ing due to a restrictive atrial septal defect (ASD). condition, with most deaths occurring in early infancy, and This results in global hypoperfusion, with pro- almost all of those affected dying before their first birthday. found hypoxaemia and acidosis, severe pulmon- ary venous hypertension, and overwhelming However, the advent of surgical palliation and advances in pulmonary venous congestion on chest x ray. peri-operative care, have offered hope to these patients These infants are generally unresponsive to and their families. measures aimed at improving pulmonary flow such as aggressive mechanical ventilation with ........................................................................... high inspired oxygen fractions or nitric oxide, and if left untreated they rapidly develop ypoplastic left heart syndrome (HLHS) is a progressive pulmonary venous hypertension. continuum which can affect all left sided This is associated with increased mortality in Hcardiac structures, from the mitral valve to infants with HLHS.34 the aortic arch. Since Norwood’s first description A restrictive ASD requires urgent intervention. of surgical palliation in 1981,1 HLHS has been If this has been diagnosed antenatally, delivery managed either by staged palliation in the should be planned in a centre able to urgently majority of cases, or, in a minority, by primary institute cardiopulmonary bypass. -
Norwood/Batista Operation for a Newborn with Dilated Myopathy of the Left Ventricle
612 Brief communications The Journal of Thoracic and Cardiovascular Surgery September 2000 NORWOOD/BATISTA OPERATION FOR A NEWBORN WITH DILATED MYOPATHY OF THE LEFT VENTRICLE Richard D. Mainwaring, MD, Regina M. Healy, BS, John D. Murphy, MD, and William I. Norwood, MD, PhD, Wilmington, Del Partial left ventriculectomy for dilated cardiomyopathy was contractile function. The variable results that have been first reported by Batista and associates1 in 1996. The rationale reported in the adult literature may reflect patient selection for this procedure is the increase in left ventricular cavity size according to the reversibility or recoverability of the underly- in the absence of compensatory left ventricular wall thickness ing disease process. that is observed in dilated cardiomyopathy. This combination Despite the substantial worldwide experience with the of factors results in an increase in wall stress per unit muscle Batista procedure in adult patients, there is limited experience mass, as predicted by the LaPlace equation. As wall stress with this procedure in children. The current case report increases, mechanical load eventually becomes nonsustain- describes the treatment of a patient in whom the diagnosis of able and contributes to further dilation of the ventricle. Partial dilated cardiomyopathy was made in utero. left ventriculectomy has been advocated as a method of Clinical summary. A female infant was recognized in restoring the balance between cavity size and wall thickness. utero as having a dilated, poorly functioning left ventricle. Fundamental to this concept is the assumption that the left Labor was induced at 36 weeks’ gestation, and she was deliv- ventricular muscle is intrinsically normal or has recoverable ered by normal, spontaneous, vaginal delivery. -
Ambulatory Event Monitors
Corporate Medical Policy Ambulatory Event Monitors File Name: a mbulatory_event_monitors Origination: 10/2000 Last CAP Review: 10/2020 Next CAP Review: 10/2021 Last Review: 10/2020 Description of Procedure or Service Various devices are available for outpatient cardiac rhythm monitoring. These devices differ in the types of monitoring leads used, the duration and continuity of monitoring, the ability to detect arrhythmias without patient intervention, and the mechanism of delivery of the information from pa tient to clinicia n. These devices may be used to evaluate symptoms suggestive of arrhythmias (eg, syncope, palpitations), and may be used to detect atrial fibrillation (AF) in patients who have undergone cardiac ablation of AF or who have a history of cryptogenic stroke. Ca rdiac monitoring is routinely used in the inpatient setting to detect acute changes in heart rate or rhythm that may need urgent response. For some clinical conditions, a more prolonged period of monitoring in the ambulatory setting is needed to detect heart rate or rhythm abnormalities that may occur infrequently. These cases may include the diagnosis of arrhythmias in patients with signs and symptoms suggestive of a rrhythmias, as well a s, the evaluation of paroxysmal a tria l fibrilla tion (AF). Arrhythmia Detection in Patients With Signs/Symptoms of Arrhythmia Ca rdiac a rrhythmias may be suspected because of symptoms suggestive of a rrhythmias, including palpitations, dizziness, or syncope or presyncope, or because of abnormal heart rate or rhythm noted on exam. A full discussion of the differential diagnosis and evaluation of each of these symptoms is beyond the scope of this review, but some general principles on the use of ambulatory monitoring are discussed. -
Pediatric Cardiac Imaging Guidelines V1.0
CLINICAL GUIDELINES Pediatric Cardiac Imaging Policy Version 1.0 Effective February 14, 2020 eviCore healthcare Clinical Decision Support Tool Diagnostic Strategies: This tool addresses common symptoms and symptom complexes. Imaging requests for individuals with atypical symptoms or clinical presentations that are not specifically addressed will require physician review. Consultation with the referring physician, specialist and/or individual’s Primary Care Physician (PCP) may provide additional insight. CPT® (Current Procedural Terminology) is a registered trademark of the American Medical Association (AMA). CPT® five digit codes, nomenclature and other data are copyright 2017 American Medical Association. All Rights Reserved. No fee schedules, basic units, relative values or related listings are included in the CPT® book. AMA does not directly or indirectly practice medicine or dispense medical services. AMA assumes no liability for the data contained herein or not contained herein. © 2019 eviCore healthcare. All rights reserved. Pediatric Cardiac Imaging Guidelines V1.0 Pediatric Cardiac Imaging Guidelines PEDCD-1: General Guidelines 3 PEDCD-2: Congenital Heart Disease 9 PEDCD-3: Heart Murmur 14 PEDCD-4: Chest Pain 16 PEDCD-5: Syncope 19 PEDCD-6: Kawasaki Disease 22 PEDCD-7: Pediatric Pulmonary Hypertension 28 PEDCD-8: Echocardiography – Other Indications 31 PEDCD-9: Cardiac MRI – Other Indications 36 PEDCD-10: CT Heart and Coronary Computed Tomography Angiography (CCTA) – Other Indications 41 PEDCD-11: Cardiac Catheterization 46 Procedure -
Impaired Cardiac Autonomic Nervous Control After Cardiac Bypass Surgery for Congenital Heart Disease૾૾૾
Impaired cardiac autonomic nervous control after cardiac bypass surgery for congenital heart disease૾૾૾, Laura McGlonea, *, Neil Patelbc , David Young , Mark D. Danton b aPrincess Royal Maternity Hospital, Alexandra Parade, Glasgow, Scotland, UK bThe Royal Hospital for Sick Children, Yorkhill, Glasgow, UK cDepartment of Medical Statistics, University of Strathclyde, Glasgow, UK Abstract We undertook a study to describe changes in heart rate variability (HRV) postoperatively in children undergoing cardiac bypass surgery for congenital heart disease (CHD). HRV was recorded for a 1-h period preoperatively and a 24-h period postoperatively in 20 children with CHD. We found a highly significant reduction in HRV in both time and frequency domain indices compared to preoperative values, which was sustained throughout the 24-h study period. There was a negative correlation between both time and frequency domain HRV measurements and length of cardiac bypass. HRV is reduced postoperatively and correlates with cardiac bypass time. Length of cardiac bypass time may be one mechanism whereby HRV is reduced following surgery. Keywords: Cardiopulmonary bypass; Congenital; Autonomic nervous system; Heart rate 1. Introduction pacemaker, or if they required cardiac pacing postopera- tively. Approval was obtained from the Local Ethics Com- ( ) Heart rate variability HRV is a measure of cardiac mittee prior to study commencement and informed autonomic nervous control. In adult patients, reductions in parental consent was obtained for all participants. HRV are independent predictors of mortality in congestive heart failure and after myocardial infarction w1–3x. In children with congenital heart disease (CHD),HRVis 2.1. HRV recording reduced compared to normal controls and is predictive of HRV was recorded for 1 h preoperatively (24–48 h prior w x sudden cardiac death 1 . -
Coders' Desk Reference for ICD-10-PCS Procedures
2 0 2 DESK REFERENCE 1 ICD-10-PCS Procedures ICD-10-PCS for DeskCoders’ Reference Coders’ Desk Reference for ICD-10-PCS Procedures Clinical descriptions with answers to your toughest ICD-10-PCS coding questions Sample 2021 optum360coding.com Contents Illustrations ..................................................................................................................................... xi Introduction .....................................................................................................................................1 ICD-10-PCS Overview ...........................................................................................................................................................1 How to Use Coders’ Desk Reference for ICD-10-PCS Procedures ...................................................................................2 Format ......................................................................................................................................................................................3 ICD-10-PCS Official Guidelines for Coding and Reporting 2020 .........................................................7 Conventions ...........................................................................................................................................................................7 Medical and Surgical Section Guidelines (section 0) ....................................................................................................8 Obstetric Section Guidelines (section