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Respiratory Care in India - Past, Present and Future

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Presentation on theme: "Respiratory Care in India - Past, Present and Future"— Presentation transcript:

1 Respiratory Care in India - Past, Present and Future
Vijay Deshpande, MS, RRT, FAARC Emeritus Professor, Georgia State University Atlanta, Georgia USA Adjunct Visiting Professor Dept. of Respiratory Therapy Dept. of Medical Technology Manipal College of Health Sciences Symbiosis Institute of Health Sciences Manipal , Karnataka Pune , Maharashtra

2 Home Respiratory Therapy
Home Oxygen Therapy Bronchodilator Therapy CPAP BiPAP Trache Care Mome Mechanicl Ventilation

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5 Frequent visits to Physician’s office High Health Care Cost
Susceptibility to infection COPD Patient Co-morbid disorders Frequent Exacerbation Mechanical Ventilation Frequent Hospitalization

6 Medicare or Reimbursement
Primary Care Physicians Medicare or Reimbursement system Pulmonologists COPD Patient Hospitals Home Care Providers Respiratory Care Dept.

7 Medicare or Reimbursement system
Primary Care Physicians Medicare or Reimbursement system Pulmonologists COPD Patient NPPV Manufacturer Hospitals Home Care Providers HMO’s

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9 HOME CARE RESPIRATORY THERAPIST

10 Home Care Nutritionist

11 Home Care Physical Therapist

12 Thank You !

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14 Home Respiratory Therapy
Asthma COPD Chronic CHF Obstructive Sleep Apnea Long Term Mechanical Ventilation

15 COPD- Definition COPD is a disease state characterized by
airflow limitation that is not fully reversible. The airflow limitation is usually both progressive and associated with an abnormal inflammatory response of the lungs to noxious particles or gases Global Initiative for Chronic Obstructive Lung Disease, National Institute of Health and National Heart, Lung and Blood Institute, NIH Publication No. 2701B, April 2001.

16 FIGURE 4-1. Normal lung volumes and capacities
FIGURE Normal lung volumes and capacities. IRV = inspiratory reserve volume; VT = tidal volume; RV = residual volume; ERV = expiratory reserve volume;TLC = total lung capacity; VC = vital capacity; IC = inspiratory capacity; FRC = functional residual capcity.

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18 PULMONARY FUNCTION TESTING
SPIROMETRY FVC SVC IC ERV VT Flowrates

19 Chronic Obstructive Pulmonary Disease
BRONCHITIS EMPHYSEMA BRONCHITIS EMPHYSEMA

20 Advancement in Management of COPD Patients
Oxygen by Nasal Cannula Oxygen via Venturi Mask E Cylinder Small Portable D cylinder Flasks Liquid Oxygen cylinder with cannula Trans-tracheal oxygen (cosmetic) Oxygen Concentrators Long Term Oxygen Therapy

21 Indications for LTOT PaO2 < 55 Hg or SaO2 < 88% on room air
PaO mm Hg and one of the following: Pulmonary hypertension and edema Cor Pulmonale Secondary Polycythemia (56%) Pulmonary restrictive disease with PaO2 < 55 mm Hg Refractory dyspnea associated with cardiac failure

22 Benefits of LTOT Improves survival in patients with
COPD and severe resting hypoxemia Decreases frequency of exacerbation of the disease requiring hospitalization Improves exercise performance

23 COPD and SLEEP Sleep studies performed on COPD patients indicate that compared to normal individuals, the COPD patients: have less hours of sleep have poorer quality of sleep have more arousal's at night

24 Obstructive Sleep Apnea and COPD
Can coexist May lead to: Oxygen desaturation during sleep Decreased ventilation V/Q mismatch ATS statement: Standards for Diagnosis and care of Patients with COPD Respiratory and Critical Care Medicine, Nov.1995, 152:S78-S121.

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26 NPPV (Bilevel Positive Airway Pressure)
20 15 PS CPAP IPAP Pressure 10 5 Time Bi-level Positive Airway Pressure

27 Be nice to your kids. They’ll choose your nursing home.

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31 Management of Advanced COPD
“We cannot add years to their life, but we can add life to their years”. 3

32 NPPV Diagnosis of COPD Need for Bronchodilator Therapy CPAP Therapy
Home Care Management of COPD Patients Diagnosis of COPD NPPV Wheezing, Increased Secretions, Abnormal Breath Sounds, Increased Airway Resistance, Use of accessory muscles Non-responsive to CPAP Therapy, Polysomnography, Identification of Sleep Apnea Need for Bronchodilator Therapy CPAP Therapy Daytime sleepiness, Somnolence, Snoring, Nocturnal Desaturation,

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35 Effect of Hypoxemia on Cardiovascular system

36 Sequence of Blood Flow Through the Heart

37 Hemodynamics and Pulmonary Vasoconstriction

38 Cardiovascular Effects of Hypoxemia
Tachycardia Pulmonary Vasoconstriction Pulmonary Hypertension Systemic Hypertension

39 COPD and Oxygen Economics
Long-term oxygen therapy (LTOT) increases survival and improves the quality of life of hypoxemic patients with chronic obstructive pulmonary disease (COPD) Each year, approximately one million patients receive LTOT through Medicare, at a cost exceeding two billion dollars per year This cost is increasing at an annual rate of nearly 13 percent The economic impact of oxygen therapy on the Medicare Budget resulted in stringent Criteria to use LTOT

40 National Lung Health Education Program, 2006
Long Term Oxygen Therapy (LTOT) History, Scientific Foundations, and Emerging Technologies Thomas L. Petty, M.D. Robert W. McCoy, B.S., RRT Dennis E. Doherty, M.D. 6th Oxygen Consensus Conference Recommendations National Lung Health Education Program, 2006

41 Long Term Oxygen Therapy
LTOT refers to delivery of oxygen therapy for continuous use at home for patients with chronic hypoxemia (PaO2 =/< 55mHg) Oxygen flow rate must be adequate to increase PaO2 above 60 mm Hg while awake. LTOT is likely to be life long LTOT is usually given for at least 15 hours daily, to include night time.

42 Indications for LTOT Chronic Hypoxemia Severe chronic Asthma
Nocturnal Hypoventilation Secondary Polycythemia Primary Pulmonary Hypertension Chronic Heart Failure Pulmonary malignancy

43 LONG TERM MANAGEMENT OF COPD PATIENTS
Absolute Indications for Long-term Oxygen Therapy PaO2 < 55 mm Hg or SaO2 < 88 % PaO2 = mm Hg or SaO2 > 89 % with: Presence of Cor Pulmonale ECG evidence of “P” pulmonale Hematocrit > 55 % Congestive Heart Failure ATS statement: Standards for Diagnosis and care of Patients with COPD Respiratory and Critical Care Medicine, Nov.1995, 152:S78-S121.

44 Physiological indications for long-term oxygen therapy (LTOT)
PaO2 mmHg SpO2 % LTOT indication Qualifying condition __________________________________________________________ ≤55 ≤88 Absolute None Relative with "P" pulmonale, qualifier polycythemia >55% History of odema ≥60 ≥90 None except Exercise desaturation with qualifier Sleep desaturation not corrected by CPAP Lung disease with severe dyspnea responding to O2

45 Oxygen Dose •Continuous flow by a double or single nasal cannulae •By demand system with demonstration of adequate oxygen saturation •Lowest liter flow to raise PO2 to mm Hg or oxygen saturation to 88-94% •Increase baseline liter flow by 1 L during exercise and sleep

46 LTOT may improve outcome measures
other than mortality, including: quality of life, cardiovascular morbidity, depression, cognitive function, exercise capacity, and frequency of hospitalization

47 When appropriately prescribed and correctly used, LTOT has clearly been shown to improve survival in hypoxemic COPD patients. Adherence to LTOT ranges from 45% to 70% and utilization for more than 15 hours per day is widely accepted as efficacious.

48 More Documented Benefits of LTOT
Two landmark studies, the Nocturnal Oxygen Therapy Trial (NOTT) and the British Medical Research Council (MRC) conducted in the late 1970s have explicitly demonstrated that LTOT (when used for more than 15 hours/day) improves survival rates in patients with severe COPD associated with resting hypoxemia [1, 2]. In terms of maximum benefit, continuous oxygen administration (≥15 h/d) is superior to intermittent or nocturnal use [3]. There is also accumulating evidence that LTOT has favourable effects on other outcome measures, including depression, cognitive function, quality of life, exercise capability, and frequency of hospitalization [4–10]. Moreover, it stabilizes and sometimes reverses the progression of pulmonary arterial hypertension and it diminishes as well cardiac arrhythmias and electrocardiographic findings indicative of myocardial ischemia [11, 12].


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