Therapeutic Exercise Foundations and Techniques

Total Page:16

File Type:pdf, Size:1020Kb

Therapeutic Exercise Foundations and Techniques 00Kisner (F)-FM 3/9/07 1:28 PM Page i Therapeutic Exercise Foundations and Techniques FIFTH EDITION 00Kisner (F)-FM 3/9/07 1:28 PM Page ii 00Kisner (F)-FM 3/9/07 1:28 PM Page iii Therapeutic Exercise Foundations and Techniques FIFTH EDITION CAROLYN KISNER, PT, MS Assistant Professor Emeritus The Ohio State University School of Allied Medical Professions Physical Therapy Division Columbus, Ohio LYNN ALLEN COLBY, PT, MS Assistant Professor Emeritus The Ohio State University School of Allied Medical Professions Physical Therapy Division Columbus, Ohio 00Kisner (F)-FM 3/9/07 1:28 PM Page iv F. A. Davis Company 1915 Arch Street Philadelphia, PA 19103 www.fadavis.com Copyright © 2007 by F. A. Davis Company Copyright © 2002, 1996, 1990, 1985 by F. A. Davis Company. All rights reserved. This product is protected by copyright. No part of it may be reproduced, stored in a retrieval system, or transmit- ted in any form or by any means, electronic, mechanical, photocopying, recording, or otherwise, without written permission from the publisher. Printed in the United States of America Last digit indicates print number: 10 9 8 7 6 5 4 3 2 1 Publisher: Margaret Biblis Manager, Content Development: Deborah J. Thorp Developmental Editor: Jennifer A. Pine Art and Design Manager: Carolyn O’Brien As new scientific information becomes available through basic and clinical research, recommended treatments and drug therapies undergo changes. The author(s) and publisher have done everything possible to make this book accurate, up to date, and in accord with accepted standards at the time of publication. The author(s), editors, and publisher are not responsible for errors or omissions or for consequences from application of the book, and make no warranty, expressed or implied, in regard to the contents of the book. Any practice described in this book should be applied by the reader in accordance with professional standards of care used in regard to the unique circumstances that may apply in each situation. The reader is advised always to check product information (package inserts) for changes and new information regarding dose and contraindications before administering any drug. Caution is especially urged when using new or infrequently ordered drugs. Library of Congress Cataloging-in-Publication Data Kisner, Carolyn. Therapeutic exercise : foundations and techniques / Carolyn Kisner, Lynn Allen Colby. — 5th ed. p. ; cm. Includes bibliographical references and index. ISBN-13: 978-0-8036-1584-7 ISBN-10: 0-8036-1584-1 1. Exercise therapy—Handbooks, manuals, etc. I. Colby, Lynn Allen. II. Title. [DNLM: 1. Exercise Therapy—methods. WB 541 K61t 2007] RM725.K53 2007 615.8′2—dc22 2007007512 Authorization to photocopy items for internal or personal use, or the internal or personal use of specific clients, is granted by F. A. Davis Company for users registered with the Copyright Clearance Center (CCC) Transactional Reporting Service, provided that the fee of $.10 per copy is paid directly to CCC, 222 Rosewood Drive, Danvers, MA 01923. For those organizations that have been granted a photocopy license by CCC, a separate system of payment has been arranged. The fee code for users of the Transactional Reporting Service is: 8036-1042-03 0 ϩ $.10. 25Kisner (F)-25 3/9/07 12:54 PM Page 851 Management of Pulmonary Conditions 25 CHAPTER REVIEW OF RESPIRATORY STRUCTURE Teaching an Effective Cough 868 AND FUNCTION 852 Additional Techniques to Facilitate a Cough and Thorax and Chest Wall: Structure Improve Airway Clearance 869 and Function 852 Suctioning: Alternative to Coughing 870 Muscles of Ventilation 852 POSTURAL DRAINAGE 870 Mechanics of Ventilation 853 Manual Techniques Used with Postural Anatomy and Function of the Drainage Therapy 870 Respiratory Tracts 854 Postural Drainage Positions 872 The Lungs and Pleurae 855 Guidelines for Implementing Postural Lung Volumes and Capacities 856 Drainage 874 EXAMINATION 856 Modified Postural Drainage 874 Components of the Examination 857 Home Program of Postural Drainage 875 BREATHING EXERCISES AND VENTILATORY MANAGEMENT OF PATIENTS WITH CHRONIC TRAINING 861 OBSTRUCTIVE PULMONARY DISEASE 875 Guidelines for Teaching Breathing Exercises 861 Types of Obstructive Pulmonary Disorders 875 Diaphragmatic Breathing 862 Pathological Changes in the Pulmonary Segmental Breathing 863 System 875 Pursed-Lip Breathing 864 Impairments and Impact on Function 875 Preventing and Relieving Episodes Management Guidelines: COPD 876 of Dyspnea 865 MANAGEMENT OF PATIENTS WITH Positive Expiratory Pressure Breathing 865 RESTRICTIVE PULMONARY DISORDERS 876 Respiratory Resistance Training 866 Acute and Chronic Causes of Restrictive Glossopharyngeal Breathing 866 Pulmonary Disorders 876 EXERCISES TO MOBILIZE THE CHEST 867 Pathological Changes in the Pulmonary Specific Techniques 867 System 876 Management Guidelines: Post-Thoracic COUGHING 868 Surgery 876 The Normal Cough Pump 868 Factors that Decrease the Effectiveness of the INDEPENDENT LEARNING ACTIVITIES 880 Cough Mechanism and Cough Pump 868 Cardiovascular and pulmonary physical therapy is a mul- Prevent airway obstruction and accumulation of secre- tifaceted area of professional practice that deals with the tions that interfere with normal respiration/oxygen management of patients of all ages with acute or chronic, transport. primary or secondary cardiovascular and pulmonary disor- Improve airway clearance, cough effectiveness, and ders. Although the cardiovascular and pulmonary systems ventilation through mobilization and drainage of are inherently linked as they interface with all other body secretions. systems, the focus of this chapter is on examination proce- Improve endurance, general exercise tolerance, and dures and therapeutic interventions used for the manage- overall well-being. ment of patients with pulmonary dysfunction. In particular, Reduce energy costs during respiration through exercise interventions and manual techniques that enhance breathing retraining. ventilation and airway clearance are presented. Prevent or correct postural deformities associated with The goals of cardiovascular and pulmonary physical pulmonary or extrapulmonary disorders. therapy for patients with respiratory dysfunction are to: Maintain or improve chest mobility. 851 25Kisner (F)-25 3/9/07 12:54 PM Page 852 852 REVIEW OF RESPIRATORY STRUCTURE AND FUNCTION All of these goals are aimed at improving a patient’s overall ability to meet necessary and desired functional demands. Treatment settings vary widely, from intensive care or postsurgical care units and extended care/subacute reha- bilitation facilities to outpatient pulmonary centers and the home setting. REVIEW OF RESPIRATORY STRUCTURE AND FUNCTION Respiration is a general term used to describe gas exchange within the body and can be categorized as either external respiration or internal respiration. Basic terms are described here but an in-depth discussion of respiratory physiology, including diffusion and perfusion, goes well beyond the FIGURE 25.1 Anterior view of the rib cage. (From Starr, J, Dalton, D: The thorax scope or purpose of this chapter. The reader is referred to and chest wall. In Levangie, PK, Norkin, CC [eds] Joint Structure and Function: A Compre- several references for further study.11,22,34,59,61 hensive Analysis, ed 4. FA Davis, Philadelphia, 2005, p 197, with permission.) External respiration describes the exchange of gas at the alveolar-capillary membrane and the pulmonary capil- laries. When a person inhales and oxygen is delivered to articulate directly with the sternum via the costal cartilage. the alveoli via the tracheobronchial tree, oxygen diffuses The eighth to tenth ribs have cartilaginous attachments to through the alveolar wall and interstitial space and into the the rib above, whereas the eleventh and twelfth are floating bloodstream through the pulmonary capillary walls. The ribs (Fig. 25.1).68 opposite occurs with carbon dioxide transport. Internal respiration describes the exchange of gas between the Muscles of Ventilation pulmonary capillaries and the cells of the surrounding tissues. Internal respiration occurs when oxygen in arterial Multiple muscles attaching to the thoracic cage have an blood diffuses from red blood cells into tissues requiring impact on the movement of air in and out of the lungs during either the inspiratory or expiratory phases of oxygen for function. The reverse occurs with carbon 8,11,68 9 dioxide transport. breathing. Box 25.1 lists the muscles of ventilation. Ventilatory muscles, also referred to as respiratory Ventilation, as it refers to the respiratory system, is the 56,68 mass exchange of air to and from the body during inspira- muscles, are classified as primary or accessory. The tion and expiration. This cyclic process requires coordinat- primary muscles of ventilation are recruited during quiet ed ventilatory muscle activity, rib cage movements, and (tidal) breathing, whereas the accessory muscles of ventila- appropriate structure and function of the upper and lower tion are only recruited during deep, forced, or labored respiratory tracts.8,22,34,59,61 breathing. During quiet inspiration the diaphragm, scalenes, and parasternals are activated.56,68 In contrast, no primary ventilatory muscles contract during resting expiration. Dur- Thorax and Chest Wall: ing deep or forced breathing different accessory muscles of Structure and Function ventilation are recruited, depending on whether inspiration or expiration is occurring, as noted in Box 25.1. The main functions of the thoracic
Recommended publications
  • Lung Abscess: Analysis of 252 Consecutive Cases Diagnosed Between 1968 and 2004
    136 Moreira JS, Camargo JJP, Felicetti JC, Goldenfun PR, Moreira ALS, Porto NS Artigo Original Abscesso pulmonar de aspiração: análise de 252 casos consecutivos estudados de 1968 a 2004* Lung abscess: analysis of 252 consecutive cases diagnosed between 1968 and 2004 JOSÉ DA SILVA MOREIRA1, JOSÉ DE JESUS PEIXOTO CAMARGO2, JOSÉ CARLOS FELICETTI2, PAULO ROBERTO GOLDENFUN3, ANA LUIZA SCHNEIDER MOREIRA4, NELSON DA SILVA PORTO2 RESUMO Objetivo: Apresentar a experiência de um serviço especializado em doenças respiratórias no manejo de casos de abscesso pulmonar de aspiração. Métodos: Descrevem-se aspectos diagnósticos e resultados terapêuticos de 252 casos consecutivos de pacientes com abscesso de pulmão, hospitalizados de 1968 a 2004. Resultados: Dos 252 casos, 209 ocorreram em homens e 43 em mulheres, com média de idade de 41,4 anos. Eram alcoolistas 70,2% dos pacientes. Tosse, expectoração, febre e comprometimento do estado geral ocorreram em mais de 97% dos casos, 64% tinham dor torácica, 30,2% hipocratismo digital, 82,5% apresentavam dentes em mau estado de conservação, 78,6% tiveram episódio de perda de consciência e 67,5% apresentavam odor fétido de secreções broncopulmonares. Em 85,3% dos casos as lesões localizavam-se nos segmentos posterior de lobo superior ou superior de lobo inferior, 96,8% delas unilateralmente. Em 24 pacientes houve associação de empiema pleural (9,5%). Flora mista foi identificada em secreções broncopulmonares ou pleurais em 182 pacientes (72,2 %). Todos os doentes foram inicialmente tratados com antibióticos (principalmente penicilina ou clindamicina) e 98,4 % deles foram submetidos à drenagem postural. Procedimentos cirúrgicos foram efetuados em 52 (20,6%) pacientes (24 drenagens de empiema, 22 ressecções pulmonares e 6 pneumostomias).
    [Show full text]
  • Respiratory – Aspiration Precautions SECTION: 9.01 Strength of Evidence Level: 3
    Respiratory – Aspiration Precautions SECTION: 9.01 Strength of Evidence Level: 3 PURPOSE: 4. Consult speech therapist for patients with Implement and educate patient/caregiver on precautions dysphagia, as needed, and as ordered by that prevent aspiration. healthcare provider. 5. Consult dietitian for diet evaluation, as needed CONSIDERATIONS: (requires physician’s order). 6. If patient receiving enteral feedings, See Digestive - 1. Precautions should be taken with all patients who Gastrostomy or Jejunostomy Tube Feeding. are unable to protect their airway to prevent the 7. Monitor patient when eating/drinking: involuntary inhalation of foreign substances, such a. Instruct family or caregiver to do the same. as gastric contents, oropharyngeal secretions, b. Observe adequacy of swallowing. food or fluids, into the tracheobronchial passages. c. SN: order ST eval for tube fed patients for 2. Patients at particular risk for aspiration include those swallow eval as appropriate. whose normal protective mechanisms are impaired. 8. Maintain calm environment when the patient is 3. Major risk factors include: eating or drinking. a. Decreased level of consciousness (confusion, 9. If patient is unable to manage own oral secretions, coma, sedation). nasopharyngeal suctioning may be indicated, b. Documented previous episode of aspiration. consult with healthcare provider and refer to c. Neuromuscular disease and structural nasopharyngeal suctioning policy as needed. abnormalities of the aerodigestive tract. 10. Keep wire cutters at HOB of patient with wired jaws d. Depressed protective reflexes (cough or gag). and instruct patient and caregiver in use. e. Presence of an endotracheal tube. 11. Notify healthcare provider immediately for any signs f. Persistently high gastric residual volumes.
    [Show full text]
  • Chest Physiotherapy Page 1 of 10
    UTMB RESPIRATORY CARE SERVICES Policy 7.3.9 PROCEDURE - Chest Physiotherapy Page 1 of 10 Chest Physiotherapy Effective: 10/12/94 Revised: 04/05/18 Formulated: 11/78 Chest Physiotherapy Purpose To standardize the use of chest physiotherapy as a form of therapy using one or more techniques to optimize the effects of gravity and external manipulation of the thorax by postural drainage, percussion, vibration and cough. A mechanical percussor may also be used to transmit vibrations to lung tissues. Policy Respiratory Care Services provides skilled practitioners to administer chest physiotherapy to the patient according to physician’s orders. Accountability/Training • Chest Physiotherapy is administered by a Licensed Respiratory Care Practitioner trained in the procedure(s). • Training must be equivalent to the minimal entry level in the Respiratory Care Service with the understanding of age specific requirements of the patient population treated. Physician's A written order by a physician is required specifying: Order Frequency of therapy. Lung, lobes and segments to be drained. Any physical or physiological difficulties in positioning patient. Cough stimulation as necessary. Type of supplemental oxygen, and/or adjunct therapy to be used. Indications This therapy is indicated as an adjunct in any patient whose cough alone (voluntary or induced) cannot provide adequate lung clearance or the mucociliary escalator malfunctions. This is particularly true of patients with voluminous secretions, thick tenacious secretions, and patients with neuro- muscular disorders. Drainage positions should be specific for involved segments unless contraindicated or if modification is necessary. Drainage usually in conjunction with breathing exercises, techniques of percussion, vibration and/or suctioning must have physician's order.
    [Show full text]
  • A Comparison of the Therapeutic Effectiveness
    A COMPARISON OF THE THERAPEUTIC EFFECTIVENESS AND ACCEPTANCE OF CONVENTIONAL POSTURAL DRAINAGE AND PERCUSSION, INTRAPULMONARY PERCUSSIVE VENTILATION AND IDGH FREQUENCY CHEST WALL COMPRESSION IN HOSPITALIZED PATIENTS WITH CYSTIC FIBROSIS A Thesis Presented in Partial Fulfillment of the Requirements for the Degree Master of Science in the Graduate School of The Ohio State University By Sarah Meredith Varekojis, B.S. ***** The Ohio State University 1998 Master's Examination Committee: Approved by Mr. F. Herbert Douce, Adviser Dr. Phil Hoberty Adviser Dr. Karen McCoy School of Allied Medical Professions ABSTRACT A significant clinical manifestation of cystic fibrosis is abnormally abundant and viscous bronchial secretions. This leads to obstruction of bronchi in the lungs and predisposes the individual to chronic pulmonary infections. Bronchopulmonary hygiene is an essential part of the care of a patient with cystic fibrosis in order to enhance mucociliary clearance. Currently, several modalities of therapy are available, including high frequency chest wall compressions (HFCC), intrapulmonary percussive ventilation (IPV) and conventional postural drainage and percussion (PD&P). This study was designed to directly compare the sputum produced with HFCC, IPV and PD&P. Twenty-seven hospitalized patients were recruited for the study. Each patient received two consecutive days of each form of therapy in random order. All therapies were delivered three times a day for thirty minutes. Any sputum produced during the treatment time was expectorated and collected. Sputum was collected for a total of sixty minutes: fifteen minutes before the treatment during aerosol delivery, during the thirty minute treatment and for fifteen minutes post therapy. Sputum expectorated during each session was weighed wet and then dried and weighed again.
    [Show full text]
  • Effects of Intrapulmonary Percussive Ventilation on Airway Mucus Clearance: a Bench Model 11/2/17, 722 AM
    Effects of intrapulmonary percussive ventilation on airway mucus clearance: A bench model 11/2/17, 7'22 AM World J Crit Care Med. 2017 Aug 4; 6(3): 164–171. PMCID: PMC5547430 Published online 2017 Aug 4. doi: 10.5492/wjccm.v6.i3.164 Effects of intrapulmonary percussive ventilation on airway mucus clearance: A bench model Lorena Fernandez-Restrepo, Lauren Shaffer, Bravein Amalakuhan, Marcos I Restrepo, Jay Peters, and Ruben Restrepo Lorena Fernandez-Restrepo, Lauren Shaffer, Bravein Amalakuhan, Marcos I Restrepo, Jay Peters, Ruben Restrepo, Division of Pediatric Critical Care, Division of Pulmonary and Critical Care, and Department of Respiratory Care, University of Texas Health Science Center and the South Texas Veterans Health Care System, San Antonio, TX 78240, United States Author contributions: All authors contributed equally to the literature search, data collection, study design and analysis, manuscript preparation and final review. Correspondence to: Dr. Bravein Amalakuhan, MD, Division of Pediatric Critical Care, Division of Pulmonary and Critical Care, and Department of Respiratory Care, University of Texas Health Science Center and the South Texas Veterans Health Care System, 7400 Merton Minter Blvd, San Antonio, TX 78240, United States. [email protected] Telephone: +1-210-5675792 Fax: +1-210-9493006 Received 2017 May 7; Revised 2017 Jun 1; Accepted 2017 Jun 30. Copyright ©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved. Open-Access: This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
    [Show full text]
  • Postural Drainage Fact Sheet 7-28-05
    Consumer Fact Sheet An Introduction to Postural Drainage & Percussion Postural Drainage and Percussion (PD & P), also known why PD & P treatments are effective, and how each lung as chest physical therapy, is a widely accepted technique segment is drained. to help people with cystic fibrosis (CF) breathe with less Draining the Lung Segments difficulty and stay healthy. PD & P uses gravity and per- cussion to loosen the thick, sticky mucus in the lungs so it The goal of PD & P is to clear mucus from each of the five can be removed by coughing. Unclogging the airways is lobes of the lungs by draining mucus into the larger air- critical to reducing the severity of lung infections. ways so that it can be coughed out. The right lung is composed of three lobes: the upper lobe, the middle lobe PD & P is easy to perform using the techniques you will and the lower lobe. The left lung is made up of only two learn here. For the child with CF, PD & P can be lobes: the upper lobe and the lower lobe. performed by physical therapists, respiratory therapists, nurses, parents, siblings and even friends. The lobes are divided into smaller divisions called seg- ments. The upper lobes on the left and right sides are PD & P is sometimes used along with other types of treat- each made up of three segments: apical, posterior and ments, such as inhaled bronchodilators and antibiotics. If anterior. The left upper lobe includes the lingual, which ordered, bronchodilators should be taken before PD & P corresponds to the middle lobe on the right.
    [Show full text]
  • 1St Quarter 2002 Medicare a Bulletin
    In This Issue... ICD-9-CM Coding for Diagnostic Tests Clarification and examples on reporting the appropriate code for these Services .... 5 New Medicare Enrollment Application New Provider Enrollment Application version CMS 855 has been implemented .... 10 Coverage of Sacral Nerve Stimulation Coverage and Billing Guidelines .............................................................................. 12 Inpatient Rehabilitation Facilities Guidelines for the Implementation of Prospective Payment System ......................... 18 End Stage Renal Disease Blood Pricing for 2002.............................................................................................. 23 Final Medical Review Policies 10060, 11600, 29540, 33282, 76075, 78460, 80061, 80162, 82270, 93224, 93350, 94010, 94240, 95115, J0150, J7190, and J9999 ................................................... 25 Respiratory Services under SNF PPS Bulletin Issues Concerning Billing for Respiratory Therapy ................................................. 81 Outpatient Prospective Payment System Clarification of Activity Therapy and Patient Education/Training Services ............ 88 Features he Medicare A Bulletin From the Medical Director 3 Tshould be shared with all Administrative 4 health care practitioners and managerial members of the General Information 5 provider/supplier staff. General Coverage 11 Publications issued after Fraud and Abuse 16 October 1, 1997, are available at no-cost from our provider Hospital Services 17 Web site at End Stage Renal Disease 23 www.floridamedicare.com.
    [Show full text]
  • Posture in Thoracic Surgery by A
    Thorax: first published as 10.1136/thx.3.3.161 on 1 September 1948. Downloaded from Thorax (1948), 3, 161. POSTURE IN THORACIC SURGERY BY A. I. PARRY BROWN From the Thoracic Surgical Unit, Harefield, Middlesex It is important in thoracic surgery to find a pneumonectomy is turned from the lateral to the position upon the operating table which will com- supine position at the end of the operation the bine good surgical access with the minimum pleural pressure on the operation side is also in- interference with respiration. Present practice creased, so that in a well-grown adult it may be favours a postero-lateral approach for most thora- necessary to aspirate 600 to 800 c.cm. of air in cotomies, and for this the patient is placed with the order to produce normal readings and to centralize gobod side of the chest under. The lateral position the mediastinum. These conditions show an is maintained by a pad against the front of the increase in the capacity of the upper hemithorax chest and by pelvic and buttock supports which at the expense of the lower in the lateral position. prevent rolling or slipping if the table is tilted. A Penman (1941), in an investigation of cases who padded wedge or pillow is sometimes placed under had " mediastinal flap," and who were treated by the thorax so as to bow the chest, opening the rib artificial pneumothorax, found the same thing, and spaces on the upper side and so facilitating the in treating mediastinal displacement he used low exposure. Sellors' " chest-rest" combines the pressures and nursed the patients as far as possible wedge and the anterior support in one piece.
    [Show full text]
  • The Short-Term Effect of Breathing Tasks Via an Incentive Spirometer on Lung Function Compared with Autogenic Drainage in Subjects with Cystic Fibrosis
    The Short-Term Effect of Breathing Tasks Via an Incentive Spirometer on Lung Function Compared With Autogenic Drainage in Subjects With Cystic Fibrosis Gil Sokol, Daphna Vilozni PhD, Ran Hakimi, Moran Lavie MD, Ifat Sarouk MD, Bat-El Bar MD, Adi Dagan MD, Miryam Ofek MD, and Ori Efrati MD BACKGROUND: Forced expiration may assist secretion movement by manipulating airway dy- namics in patients with cystic fibrosis (CF). Expiratory resistive breathing via a handheld incentive spirometer has the potential to control the expiratory flow via chosen resistances (1–8 mm) and thereby mobilize secretions and improve lung function. Our objective was to explore the short-term effect of using a resistive-breathing incentive spirometer on lung function in subjects with CF compared with the autogenic drainage technique. METHODS: This was a retrospective study. ؍ Subjects with CF performed 30–45 min of either the resistive-breathing incentive spirometer (n technique on separate days. The spirometer encourages the (32 ؍ or autogenic drainage (n (40 patient to exhale as long as possible while maintaining a low lung volume. The autogenic drainage technique includes repetitive inspiratory and expiratory maneuvers at various tidal breathing magnitudes while exhalation is performed in a sighing manner. Spirometry was performed before and 20–30 min after the therapy. RESULTS: Use of a resistive-breathing incentive spirometer improved FVC and FEV1 by 5–42% in 26 subjects. The forced expiratory flow during the middle half of the FVC maneuver (FEF25-75%) improved by >20% in 9 (22%) subjects. FVC improved the most in subjects with an FEV1 of 40–60% of predicted.
    [Show full text]
  • Facility Reimbursement of Respiratory Therapy Services
    Manual: Reimbursement Policy Policy Title: Facility Reimbursement of Respiratory Therapy Services Section: Facility-Specific Subsection: Inpatient Date of Origin: 4/19/2017 Policy Number: RPM047 Last Updated: 7/12/2021 Last Reviewed: 7/14/2021 Scope This policy applies to all Commercial medical plans, Medicare Advantage plans, and Oregon Medicaid plans. This policy applies to inpatient hospital facilities. For contracted facilities, this policy is effective for dates of service 10/01/2017. For out of network facilities, this policy is effective upon initial publication. Reimbursement Guidelines A. General Policy Statements 1. In the inpatient hospital setting Moda Health will limit reimbursement for Respiratory Services to one unit/charge per date of service for each of the following categories of services: a. Respiratory therapy performed by a Respiratory Therapist(s), regardless of the number of times per day a Respiratory Therapist(s) provides care or therapy services. b. Ventilator (invasive or non-invasive) management, regardless of the number of times a Respiratory Therapist(s) reviews the equipment settings Additional units or charges for the same date of service are not eligible for separate reimbursement, regardless of the description variations, HCPCS codes, or revenue codes used. 2. Any respiratory services performed by a registered nurse (RN), are considered part of room and board, and are not eligible to be separately reported or reimbursed. 3. Inpatient hospitals will not be reimbursed, nor allowed to retain reimbursement for services considered to be non-reimbursable or not eligible for separate reimbursement. B. Documentation requirements: In the inpatient hospital setting, Respiratory Therapy must be supported by the following documentation: 1.
    [Show full text]
  • Cystic Fibrosis: Current Trends in Respiratory Care Jeffrey S Wagener MD and Aree a Headley RRT
    Cystic Fibrosis: Current Trends in Respiratory Care Jeffrey S Wagener MD and Aree A Headley RRT Introduction Cystic Fibrosis Lung Disease Diagnosis Clinical Monitoring Pulmonary Function Monitoring Radiographic Monitoring Aerosol Therapies and Delivery Devices Inhaled Bronchodilators Inhaled Anti-inflammatory Agents Inhaled Mucolytics Inhaled Antibiotics Delivery Devices Airway Clearance Techniques Chest Physiotherapy Active Cycle of Breathing Autogenic Drainage Positive Expiratory Pressure and Flutter Intrapulmonary Percussive Ventilation High-Frequency Chest Compression Exercise Noninvasive Ventilation Summary Cystic fibrosis is a genetic disease that typically produces malnutrition and chronic respiratory infections. Prolonged bronchial obstruction, infection, and inflammation result in bronchiectstasis and permanent lung damage. Most cystic fibrosis patients die because of this progressive respira- tory disease. Thus, in the absence of a cure, effective respiratory therapy is the primary means to extend and improve the quality of life for the cystic fibrosis patient. Aerosol therapy, airway clearance techniques, and noninvasive ventilation can all improve quality of life and possibly extend survival. Close patient monitoring with pulmonary function testing, chest radiography, and induced sputum can result in earlier treatment, potentially reducing permanent lung damage. Earlier diagnosis has prevented serious complications through early initiation of preventive therapies such as improved nutrition. Key words: pediatric, respiratory,
    [Show full text]
  • (HCP): Use of the Airway Dome
    Instructions for Healthcare Provider (HCP): Use of the Airway Dome. The U.S. Food and Drug Administration has issued an Emergency Use Authorization (EUA) for the Airway Dome, for use by healthcare providers (HCP) as an additional layer of barrier protection in addition to personal protective equipment (PPE) to prevent HCP exposure to pathogenic biological airborne particulates by providing isolation of hospitalized patients with suspected or confirmed diagnosis of COVID-19, at the time of definitive airway management, when performing airway-related medical procedures, or during certain transport of such patients during the COVID-19 pandemic. HCP should follow these instructions, as well as procedures at their healthcare facility to use the Airway Dome. Authorized non-transport use of Airway Dome is only for airway management (e.g., intubation, extubation and suctioning airways), or when performing any airway-related medical procedures (e.g., high flow nasal cannula oxygen treatments, nebulizer treatments, manipulation of oxygen mask or CPAP/BiPAP (continuous positive airway pressure/bi-level positive airway pressure) mask use, airway suctioning, percussion and postural drainage). Authorized use of the Airway Dome during patient transport is only within a hospital setting for temporary transfer with direct admission within the hospital in the presence of a registered nurse or physician. The patient should have constant monitoring of vital signs, electrocardiogram (EKG), SpO2% (oxygen saturation), End tidal carbon dioxide (EtCO2) if available throughout transport. For all authorized uses, the patient should always have supplemental oxygen during use of the Airway Dome. The Airway Dome has not been FDA-approved or cleared for this use; The Airway Dome has been authorized only for the duration of the declaration that circumstances exist justifying the authorization of the emergency use of medical devices under section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C.
    [Show full text]