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Oxygen and Oxygen Equipment Local Coverage Determination (LCD)
Local Coverage Determination (LCD): Oxygen and Oxygen Equipment (L33797) Links in PDF documents are not guaranteed to work. To follow a web link, please use the MCD Website. Contractor Information CONTRACTOR NAME CONTRACT TYPE CONTRACT JURISDICTION STATE(S) NUMBER CGS Administrators, LLC DME MAC 17013 - DME MAC J-B Illinois Indiana Kentucky Michigan Minnesota Ohio Wisconsin CGS Administrators, LLC DME MAC 18003 - DME MAC J-C Alabama Arkansas Colorado Florida Georgia Louisiana Mississippi New Mexico North Carolina Oklahoma Puerto Rico South Carolina Tennessee Texas Virgin Islands Virginia West Virginia Noridian Healthcare Solutions, DME MAC 16013 - DME MAC J-A Connecticut LLC Delaware District of Columbia Maine Maryland Massachusetts New Hampshire New Jersey New York - Entire State Pennsylvania Rhode Island Vermont CONTRACTOR NAME CONTRACT TYPE CONTRACT JURISDICTION STATE(S) NUMBER Noridian Healthcare Solutions, DME MAC 19003 - DME MAC J-D Alaska LLC American Samoa Arizona California - Entire State Guam Hawaii Idaho Iowa Kansas Missouri - Entire State Montana Nebraska Nevada North Dakota Northern Mariana Islands Oregon South Dakota Utah Washington Wyoming LCD Information Document Information LCD ID Original Effective Date L33797 For services performed on or after 10/01/2015 LCD Title Revision Effective Date Oxygen and Oxygen Equipment For services performed on or after 08/02/2020 Proposed LCD in Comment Period Revision Ending Date N/A N/A Source Proposed LCD Retirement Date DL33797 N/A AMA CPT / ADA CDT / AHA NUBC Copyright Notice Period Start Date Statement 06/18/2020 CPT codes, descriptions and other data only are copyright 2019 American Medical Association. All Rights Notice Period End Date Reserved. -
Chronic Cough, Shortness of Breathe, Wheezing? What You Should
CHRONIC COUGH, SHORTNESS OF BREATH, WHEEZING? WHAT YOU SHOULD KNOW ABOUT COPD. A quick guide on Chronic Obstructive Pulmonary Disease COPD.nhlbi.nih.gov COPD, or chronic obstructive Most often, COPD occurs in people pulmonary disease, is a serious lung age 40 and over who… disease that over time makes it hard • Have a history of smoking to breathe. Other names for COPD include • Have had long-term exposure to lung irritants chronic bronchitis or emphysema. such as air pollution, chemical fumes, or dust from the environment or workplace COPD, a leading cause of death, • Have a rare genetic condition called alpha-1 affects millions of Americans and causes antitrypsin (AAT) deficiency long-term disability. • Have a combination of any of the above MAJOR COPD RISK FACTORS history of SMOKING AGE 40+ RARE GENETIC CONDITION alpha-1 antitrypsin (AAT) deficiency LONG-TERM exposure to lung irritants WHAT IS COPD? To understand what COPD is, we first The airways and air sacs are elastic (stretchy). need to understand how respiration When breathing in, each air sac fills up with air like and the lungs work: a small balloon. When breathing out, the air sacs deflate and the air goes out. When air is breathed in, it goes down the windpipe into tubes in the lungs called bronchial In COPD, less air flows in and out of tubes or airways. Within the lungs, bronchial the airways because of one or more tubes branch into thousands of smaller, thinner of the following: tubes called bronchioles. These tubes end in • The airways and air sacs lose bunches of tiny round air sacs called alveoli. -
Guía Práctica Clínica Bronquiolitis.Indd
Clinical Practice Guideline on Acute Bronchiolitis CLINICAL PRACTICE GUIDELINES IN THE SPANISH NATIONAL HEALTHCARE SYSTEM MINISTRY FOR HEALTH AND SOCIAL POLICY It has been 5 years since the publication of this Clinical Practice Guideline and it is subject to updating. Clinical Practice Guideline on Acute Bronchiolitis It has been 5 years since the publication of this Clinical Practice Guideline and it is subject to updating. CLINICAL PRACTICE GUIDELINES IN THE SPANISH NATIONAL HEALTHCARE SYSTEM MINISTRY FOR HEALTH AND SOCIAL POLICY This CPG is an aid for healthcare decisions. It is not binding, and does not replace the clinical judgement of healthcare staff. Published: 2010 It has beenPublished 5 years by: Ministry since for theScience publication and Innovation of this Clinical Practice Guideline and it is subject to updating. NIPO (Official Publication Identification No.): 477-09-055-4 ISBN: pending Legal depository: B-10297-2010 Printed by: Migraf Digital This CPG has been funded via an agreement entered into by the Carlos III Health Institute, an autonomous body within the Spanish Ministry for Science and Innovation, and the Catalan Agency for Health Technology Assessment, within the framework for cooperation established in the Quality Plan for the Spanish National Healthcare System of the Spanish Ministry for Health and Social Policy. This guideline must be cited: Working Group of the Clinical Practice Guideline on Acute Bronchiolitis; Sant Joan de Déu Foundation Fundació Sant Joan de Déu, coordinator; Clinical Practice Guideline on Acute Bronchiolitis; Quality Plan for the Spanish National Healthcare System of the Spanish Ministry for Health and Social Policy; Catalan Agency for Health Technology Assessment, 2010; Clinical Practice Guidelines in the Spanish National Healthcare System: CAHTA no. -
Coding Billing
CodingCoding&Billing FEBRUARY 2020 Quarterly Editor’s Letter Welcome to the February issue of the ATS Coding and Billing Quarterly. There are several important updates about the final Medicare rules for 2020 that will be important for pulmonary, critical care and sleep providers. Additionally, there is discussion of E/M documentation rules that will be coming in 2021 that practices might need some time to prepare for, and as always, we will answer coding, billing and regulatory compliance questions submitted from ATS members. If you are looking for a more interactive way to learn about the 2020 Medicare final rules, there is a webinar on the ATS website that covers key parts of the Medicare final rules. But before we get to all this important information, I have a request for your help. EDITOR ATS Needs Your Help – Recent Invoices for Bronchoscopes and PFT Lab ALAN L. PLUMMER, MD Spirometers ATS RUC Advisor TheA TS is looking for invoices for recently purchased bronchoscopes and ADVISORY BOARD MEMBERS: PFT lab spirometer. These invoices will be used by theA TS to present practice KEVIN KOVITZ, MD expense cost equipment to CMS to help establish appropriate reimbursement Chair, ATS Clinical Practice Committee rates for physician services using this equipment. KATINA NICOLACAKIS, MD Member, ATS Clinical Practice Committee • Invoices should not include education or service contract as those ATS Alternate RUC Advisorr are overhead and cannot be considered by CMS for this portion of the STEPHEN P. HOFFMANN, MD Member, ATS Clinical Practice Committee formula and payment rates. ATS CPT Advisor • Invoices can be up to five years old. -
Management of Airway Obstruction and Stridor in Pediatric Patients
November 2017 Management of Airway Volume 14, Number 11 Obstruction and Stridor in Authors Ashley Marchese, MD Department of Pediatrics, Yale-New Haven Hospital, New Haven, CT Pediatric Patients Melissa L. Langhan, MD, MHS Associate Professor of Pediatrics and Emergency Medicine; Fellowship Director, Director of Education, Pediatric Emergency Abstract Medicine, Yale University School of Medicine, New Haven, CT Peer Reviewers Stridor is a result of turbulent air-flow through the trachea from Steven S. Bin, MD upper airway obstruction, and although in children it is often Associate Clinical Professor of Emergency Medicine and Pediatrics; Medical Director, Emergency Department, UCSF School of Medicine, due to croup, it can also be caused by noninfectious and/or con- Benioff Children’s Hospital, San Francisco, CA genital conditions as well as life-threatening etiologies. The his- Alexander Toledo, DO, PharmD, FAAEM, FAAP tory and physical examination guide initial management, which Chief, Section of Pediatric Emergency Medicine; Director, Pediatric Emergency Department, Arizona Children’s Center at Maricopa includes reduction of airway inflammation, treatment of bacterial Medical Center, Phoenix, AZ infection, and, less often, imaging, emergent airway stabilization, Prior to beginning this activity, see “Physician CME Information” or surgical management. This issue discusses the most common on the back page. as well as the life-threatening etiologies of acute and chronic stridor and its management in the emergency department. Editor-in-Chief -
Interstitial Lung Disease—Raising the Index of Suspicion in Primary Care
www.nature.com/npjpcrm All rights reserved 2055-1010/14 PERSPECTIVE OPEN Interstitial lung disease: raising the index of suspicion in primary care Joseph D Zibrak1 and David Price2 Interstitial lung disease (ILD) describes a group of diseases that cause progressive scarring of the lung tissue through inflammation and fibrosis. The most common form of ILD is idiopathic pulmonary fibrosis, which has a poor prognosis. ILD is rare and mainly a disease of the middle-aged and elderly. The symptoms of ILD—chronic dyspnoea and cough—are easily confused with the symptoms of more common diseases, particularly chronic obstructive pulmonary disease and heart failure. ILD is infrequently seen in primary care and a precise diagnosis of these disorders can be challenging for physicians who rarely encounter them. Confirming a diagnosis of ILD requires specialist expertise and review of a high-resolution computed tomography scan (HRCT). Primary care physicians (PCPs) play a key role in facilitating the diagnosis of ILD by referring patients with concerning symptoms to a pulmonologist and, in some cases, by ordering HRCTs. In our article, we highlight the importance of prompt diagnosis of ILD and describe the circumstances in which a PCP’s suspicion for ILD should be raised in a patient presenting with chronic dyspnoea on exertion, once more common causes of dyspnoea have been investigated and excluded. npj Primary Care Respiratory Medicine (2014) 24, 14054; doi:10.1038/npjpcrm.2014.54; published online 11 September 2014 INTRODUCTION emphysema, in which the airways of the lungs become narrowed Interstitial lung disease (ILD) is an umbrella term, synonymous or blocked so the patient cannot exhale completely. -
Prilocaine Induced Methemoglobinemia Güzelliğin Bedeli; Prilokaine Bağlı Gelişen Methemoglobinemi Olgusu
CASE REPORT 185 Cost of Beauty; Prilocaine Induced Methemoglobinemia Güzelliğin Bedeli; Prilokaine Bağlı Gelişen Methemoglobinemi Olgusu Elif KILICLI, Gokhan AKSEL, Betul AKBUGA OZEL, Cemil KAVALCI, Dilek SUVEREN ARTUK Department of Emergency Medicine, Baskent University Faculty of Medicine, Ankara SUMMARY ÖZET Prilocaine induced methemoglobinemia is a rare entity. In the pres- Prilokaine bağlı gelişen methemoglobinemi nadir görülen bir du- ent paper, the authors aim to draw attention to the importance of rumdur. Bu yazıda epilasyon öncesi kullanılan prilokaine sekonder this rare condition by reporting this case. A 30-year-old female gelişen methemoglobinemi olgusunu sunarak nadir görülen bu presented to Emergency Department with headache, dispnea and durumun önemine işaret etmek istiyoruz. Otuz yaşında kadın acil cyanosis. The patient has a history of 1000-1200 mg of prilocaine servise baş ağrısı, dispne ve siyanoz şikayetleri ile başvurdu. Hasta- ya beş saat öncesinde bir güzellik merkezinde epilasyon öncesinde subcutaneous injection for hair removal at a beauty center, 5 hours yaklaşık 1000-1200 mg prilokain subkutan enjeksiyonu yapıldığı ago. Tension arterial: 130/73 mmHg, pulse: 103/minute, body tem- öğrenildi. Başvuruda kan basıncı 130/73 mmHg, nabız 103/dk, vü- perature: 37 °C and respiratory rate: 20/minute. The patient had ac- cut ısısı 37 °C ve solunum sayısı 20/dk olarak kaydedilmişti. Hasta- ral and perioral cyanosis. Methemoglobin was measured 14.1% in nın akral siyanozu belirgindi. Venöz kan gazında methemoglobin venous blood gas test. The patient treated with 3 gr ascorbic acid düzeyi %14.1 olarak ölçüldü. Hastaya 3 g intravenöz askorbik asit intravenously. The patient was discharged free of symptoms after uygulandı. -
Submitting Requests for Prior Authorization
Molina Healthcare/Molina Medicare of California Prior Authorization/Pre-Service Review Guide Effective: 08/01/2012 This Prior Authorization/Pre-Service Guide applies to all Molina Healthcare/Molina Medicare Members /Sacrament LIHP. ***Referrals to Network Specialists do not require Prior Authorization*** Authorization required for services listed below. Pre-Service Review is required for elective services. Only covered services will be paid. If you are contracted with Molina through an IPA / Medical Group please refer to your IPA / MG Prior Authorization requirements. For San Diego Medi-Cal members age 0 – 17.99 years old please refer to Children’s Physicians Medical Group’s (CPMG) Prior Authorization requirements. All Non-Par providers/services: services, including office Hearing Aids – including bone anchored hearing aids. visits, provided by non-participating providers, facilities and Not a covered benefit for Sacramento LIHP labs, except professional services related to ER visit, approved Home Healthcare: after initial 3 skilled nursing Ambulatory Surgical Center or inpatient stay and Women’s visits health/OB services. ER visits do not require PA Home Infusion Alcohol and Chemical Dependency Services (Medicare & Outpatient Hospice & Palliative Care: notification CHIP only) Refer to Comp Care or Behavioral Health contact information – page 3 only. All Inpatient Admissions: Acute hospital, SNF, Rehab, Not a covered benefit for Sacramento LIHP LTACS, Hospice(notification only) Behavioral Health Services: - Inpatient, Partial Imaging: CT, MRI, MRA, PET, SPECT, Cardiac Nuclear hospitalization, Day Treatment, Intensive Outpatient Programs Studies, CT Angiograms, intimal media thickness (IOP), ECT, and > 12 Office Visits/year for adults and 20 Office testing, three dimensional imaging visits/year for children (Medicare & CHIP only) Refer to Behavioral Neuropsychological Testing and Therapy. -
Shanti Bhavan Medical Center Biru, Jharkhand, India
Shanti Bhavan Medical Center Biru, Jharkhand, India We Care, He Heals Urgent Needs 1. Boundary Wall around the hospital property Cost: $850,000 In India any land (even owned) can be taken by the government at any time if there is not boundary wall around it. Our organization owns property around the hospital that is intended for the Nursing school and other projects. We need a boundary wall built around the land so that the government can’t recover the land. 2. Magnetic Resonance Imaging Device Cost: $300,000 Magnetic resonance imaging (MRI) is a medical imaging technique used in radiology to form pictures of the anatomy and the physiological processes of the body in both health and disease. MRI scanners use strong magnetic fields, radio waves, and field gradients to generate images of the organs in the body. 3. Kidney Stone Lipotriptor Cost: $200,000 Kidney Stone Lipotriptor Extracorporeal Shock Wave Lithotripsy (ESWL) is the least invasive surgical stone treatment using high frequency sound waves from an external source (outside the body) to break up kidney stones into smaller pieces, and allow them to pass out through the urinary tract. 4. Central Patient Monitoring System Cost: $28,000 Central Patient Monitoring System- A full-featured system that provides comprehensive patient monitoring and review. Monitors up to 32 patients using two displays and is ideal for telemetry, critical care, OR, emergency room, and other monitoring environments. Provides data storage and review capabilities, and ensures a complete patient record by facilitating automated patient and data transfer between multiple departments. 5. ABG Machine Cost: $25,000 ABG machine- An arterial blood gas test (ABG) is a blood gas test of blood taken from an artery that measures the amounts of certain gases (such as oxygen and carbon diox- ide) dissolved in arterial blood. -
How Is Pulmonary Fibrosis Diagnosed?
How Is Pulmonary Fibrosis Diagnosed? Pulmonary fibrosis (PF) may be difficult to diagnose as the symptoms of PF are similar to other lung diseases. There are many different types of PF. If your doctor suspects you might have PF, it is important to see a specialist to confirm your diagnosis. This will help ensure you are treated for the exact disease you have. Health History and Exam Your doctor will perform a physical exam and listen to your lungs. • If your doctor hears a crackling sound when listening to your lungs, that is a sign you might have PF. • It is also important for your doctor to gather detailed information about your health. ⚪ This includes any family history of lung disease, any hazardous materials you may have been exposed to in your lifetime and any diseases you’ve been treated for in the past. Imaging Tests Tests like chest X-rays and CT scans can help your doctor look at your lungs to see if there is any scarring. • Many people with PF actually have normal chest X-rays in the early stages of the disease. • A high-resolution computed tomography scan, or HRCT scan, is an X-ray that provides sharper and more detailed pictures than a standard chest X-ray and is an important component of diagnosing PF. • Your doctor may also perform an echocardiogram (ECHO). ⚪ This test uses sound waves to look at your heart function. ⚪ Doctors use this test to detect pulmonary hypertension, a condition that can accompany PF, or abnormal heart function. Lung Function Tests There are several ways to test how well your lungs are working. -
Weaning from Tracheostomy in Subjects Undergoing Pulmonary
Pasqua et al. Multidisciplinary Respiratory Medicine (2015) 10:35 DOI 10.1186/s40248-015-0032-1 ORIGINALRESEARCHARTICLE Open Access Weaning from tracheostomy in subjects undergoing pulmonary rehabilitation Franco Pasqua1,2*, Ilaria Nardi1, Alessia Provenzano1, Alessia Mari1 on behalf of the Lazio Regional Section, Italian Association of Hospital Pulmonologists (AIPO) Abstract Background: Weaning from tracheostomy has implications in management, quality of life, and costs of ventilated patients. Furthermore, endotracheal cannula removing needs further studies. Aim of this study was the validation of a protocol for weaning from tracheostomy and evaluation of predictor factors of decannulation. Methods: Medical records of 48 patients were retrospectively evaluated. Patients were decannulated in agreement with a decannulation protocol based on the evaluation of clinical stability, expiratory muscle strength, presence of tracheal stenosis/granulomas, deglutition function, partial pressure of CO2, and PaO2/FiO2 ratio. These variables, together with underlying disease, blood gas analysis parameters, time elapsed with cannula, comordibity, Barthel index, and the condition of ventilation, were evaluated in a logistic model as predictors of decannulation. Results: 63 % of patients were successfully decannulated in agreement with our protocol and no one needed to be re-cannulated. Three variables were significantly associated with the decannulation: no pulmonary underlying diseases (OR = 7.12; 95 % CI 1.2–42.2), no mechanical ventilation (OR = 9.55; 95 % CI 2.1–44.2) and period of tracheostomy ≤10 weeks (OR = 6.5; 95 % CI 1.6–27.5). Conclusions: The positive course of decannulated patients supports the suitability of the weaning protocol we propose here. The strong predictive role of three clinical variables gives premise for new studies testing simpler decannulation protocols. -
Pulmonary Rehabilitation Improves Survival in Patients with Idiopathic
www.nature.com/scientificreports OPEN Pulmonary rehabilitation improves survival in patients with idiopathic pulmonary fbrosis undergoing lung Received: 24 October 2018 Accepted: 21 May 2019 transplantation Published: xx xx xxxx Juliessa Florian1,2,3, Guilherme Watte2,3, Paulo José Zimermann Teixeira3,4, Stephan Altmayer5, Sadi Marcelo Schio2, Letícia Beatriz Sanchez2, Douglas Zaione Nascimento2, Spencer Marcantonio Camargo2, Fabiola Adélia Perin2, José de Jesus Camargo2, José Carlos Felicetti2 & José da Silva Moreira1 This study was conducted to evaluate whether a pulmonary rehabilitation program (PRP) is independently associated with survival in patients with idiopathic pulmonary fbrosis (IPF) undergoing lung transplant (LTx). This quasi-experimental study included 89 patients who underwent LTx due to IPF. Thirty-two completed all 36 sessions in a PRP while on the waiting list for LTx (PRP group), and 53 completed fewer than 36 sessions (controls). Survival after LTx was the main outcome; invasive mechanical ventilation (IMV), length of stay (LOS) in intensive care unit (ICU) and in hospital were secondary outcomes. Kaplan-Meier curves and Cox regression models were used in survival analyses. Cox regression models showed that the PRP group had a reduced 54.0% (hazard ratio = 0.464, 95% confdence interval 0.222–0.970, p = 0.041) risk of death. A lower number of patients in the PRP group required IMV for more than 24 hours after LTx (9.0% vs. 41.6% p = 0.001). This group also spent a mean of 5 days less in the ICU (p = 0.004) and 5 days less in hospital (p = 0.046). In conclusion, PRP PRP completion halved the risk of cumulative mortality in patients with IPF undergoing unilateral LTx Idiopathic pulmonary fbrosis (IPF) is a non-reversible fbrotic lung disease characterized by a progressive decline of lung function, with a largely unpredictable clinical course and a median survival time of 2–3 years from diag- nosis1,2.