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Introduction
Cigarette smoking is the primary cause of COPD.
In 1990 ,COPD was ranked 12th as burden of disease, by 2020 it is projected to rank 5th
COPD is the only chronic disease that is showing progressive upward trend in both mortality and morbidity
Despite this burden, COPD is a Cinderella condition that receives limited recognition from both patients and physicians
GOLD
Global Initiative For Chronic Obstructive Lungs Diseases
Formed by WHO & US National Heart, Lung & Blood (NHLB) Institute.
GOLD formed
to standardize recommendations for diagnosis and management of COPD worldwide
GOLD
Increase awareness of COPD
Definition. contd
Chronic bronchitis , defined as the presence of cough and sputum production for at least 3 months in each of 2 consecutive years, is not necessarily associated with airflow limitation. Emphysema, defined as destruction of the alveoli, is a pathological term that is sometimes (incorrectly) used clinically and describes only one of several structural abnormalities present in patients with COPD
Symptoms of COPD
Cough Sputum production Dyspnea on exertion
Chronic cough and sputum production often precede the development of airflow limitation by many years, although not all individuals with cough and sputum production go on to develop COPD
Risk is related to the total burden of inhaled particles a person encounters over his lifetime
A Toxic Cocktail
ASTHMA
Allergens
COPD
Cigarette smoke
Ep cells
Mast cell
Eosinophil
Neutrophil
Bronchoconstriction AHR
LUNG INFLAMMATION
Anti-oxidants
Oxidative stress
Anti-proteinases
Proteinases
Repair mechanisms
COPD PATHOLOGY
T Lymphocyte CD8
Neutrophils
Eosinophils
Asthma
Sensitizing agent (mite, dust, Pollen)
COPD
Noxious agent (Smoking)
Diagnosing COPD
Consider COPD, and perform spirometry, if any of these indicators are present in a person over age 40.
Progressive (worsens over time) Usually worse with exercise Persistent (present every day) Described by the patient as an increased effort to breathe, heaviness, air hunger, or gasping.
Chronic Cough:
may be intermittent and may be unproductive
Spirometry
When performing spirometry, measure:
Forced Vital Capacity (FVC), Forced Expiratoory Volume in one second (FEV1) Calculate the FEV1/FVC ratio. Spirometric results are expressed as % predicted using appropriate normal values for the persons sex, age, and height Patients with COPD typically show a decrease in bothFEV1 and FEV1/FVC ratio. Post bronchodilator FEV1 is recommended for the diagnosis and assessment of severity of COPD
At risk
Mild COPD
>0.7
<0.7
>80
>80
Moderate COPD
Severe COPD Very severe COPD
<0.7
<0.7 <0.7
50-80
30-50 <30
SPIROMETRY is not to substitute for clinical judgment in the evaluation of the severity of disease in individual patients.
Physical signs
Large barrel shaped chest (hyperinflation) Prominent accessory respiratory muscles in neck and use of accessory muscle in respiration Low, flat diaphragm Diminished breath sound
Spirometry
Differential diagnosis
Asthma early onset, symptoms vary, family history, allergy, rhinitis, eczema may be present Congestive heart failure
basilar creps, CxR shows dilated heart, pulmonary edema
Bronchiectasis
Large volumes of sputum Clubbing
Tuberculosis
Any age Abnormal CxR
High local prevalence
Obliterative bronchiolitis
Younger age, nonsmoker May have history of RA, fume exposure CT on expiration shows hypodense areas
Diffuse panbronchiolitis
Male and non smokers Almost all have chronic sinusitis CT and chest x-ray shows diffuse small centrilobluar nodular opacities and hyperinflation
Relieve symptoms Prevent progression of disease Improve exercise tolerance Improve health status Prevent and treat complications Prevent and treat exacerbations Reduce mortality Prevent or minimize side effects from treatment Cessation of cigarette smoking should be included as a goal throughout the management program
Education Pharmacologic
Non-pharmacologic
4. Manage exacerbations
COPD is usually a progressive disease. Lung function can be expected to worsen over time, even with the best available care. Symptoms and lung function should be monitored to follow the development of complications, to guide treatment, and to facilitate discussion of management options with the patient. Comorbidities are common and should be actively identified
Initiate oxygen in patients with stage IV: very severe COPD if:
PaO2 is at or below7.3 kPa (55 mm hg) or Sao2 is at or below 88%, with or without hypercapnia or PO2 is between 7.3 kPa (55 mm Hg) and 8.0 kPa (60 mm Hg) or SaO2 is 88%, and if there is evidence of pulmonary hypertension, peripheral edema suggesting CHF, or polycythaemia (HCT >55%)
Surgical treatment
Bullectomy Lung Volume reduction surgery (LVRS)
4. Manage Exacerbations
Acute Exacerbation:
Acute exacerbation of COPD is defined as an event in the natural course of disease characterized by a change in the patients baseline dyspnoea, cough, and/or sputum that is beyond normal day-to-day variations, is acute in onset and may warrant a change in regular medication in a patient with underlying COPD.
Laboratory Parameters
1. 2. 3. 4. 5. Spirometry ABG CXR ECG Others
Clinical Parameters
Symptoms
Increase in
1. 2. 3. 4. 5. 6. Breathlessness Chest tightness Wheeze Cough & sputum with change of color Fever Other nonspecific symptoms
Clinical Parameters
Physical signs
1. 2. 3. 4. 5. 6. 7.
contd..
Signs of hyperinflation of lung Signs of Respiratory failure Signs of infection Signs of cor-pulmonale Paradoxical chest wall movements Haemodinamically instability Reduced alertness
Laboratory Parameters
Spirometry
PEFR < 100 L /min. or FEV1 < 1.00 L -- indicates a severe exacerbation
ABG
PaO2 < 60 mm of Hg and/or SaO2 < 90% when breathing in room air -indicates respiratory failure PaO2 < 50 mm of Hg, PaCO2 > 70 mm of Hg & PH < 7.3 --indicates a life threatening attack
Laboratory Parameters
CXR (P/A & Lateral)
-- to exclude other causes of dyspnoea
contd..
ECG
-- to exclude RVH, arrhythmia, IHD, pulmonary embolism
Spiral CT scan
Management
Home management
Hospital management
a) Management in emergency dept. b) Management in ICU
Home Management
Bronchodilator therapy
a) Increase dose & frequency b) Addition of anti-cholinergics c) Theophylline
Oral Glucocorticoids
40 mg prednisolone for 10 days
Antibiotic treatment
Oral Treatment Alternative treatment Parenteral treatment
Group-A: Patients not No antibiotic for only Co-amoxiclav; needing hospitalization one cardinal Macrolides; (mild COPD) symptom. If indicated Cephalosporins than beta-lactum, tetracycline, trimethprim/ sulfamethoxaole Group-B: Patients admitted to hospital (moderate to severe COPD without risk of P. aeruginosa) Co-amoxiclav Fluoroquinolones Co-amoxiclav; Cephalosporins; Fluoroquinolones
Group-C: Patients admitted to hospital (moderate to severe COPD with risk of P. aeruginosa)
Fluoroquinolone
Hospital Management
Indications for Hospital admission Marked increase in intensity of symptoms specially resting
dyspnea Failure to respond to initial home management Onset of new physical signs, e.g. Cyanosis, Peripheral edema Significant co-morbidities Insufficient home support Newly occurring arrhythmias
therapy repeat ABG after 30 min. Bronchodilations : a) Increase dose & frequency b) Add anticholinergics c) Intravenous methyl xanthines Add Glucocorticoids IV/ oral Antibiotics IV/ oral NIPPV Monitor fluid balance & nutrition Treat associated conditions, e.g.. heart failure / arrhythmias Closely monitor condition of the patient
Hospital Management
contd..
Management in ICU
Previous management of emergency
Room + Ventilatory support
a) Non-invasive (NIPPV) b) Invasive mechanical ventilation
Management in ICU
Selection criteria for NIPPV
(at least 2 should be present)
contd..
a) Moderate to severe dyspnoea with use of accessory muscles & paradoxical abdominal motion b) Moderate to severe acidosis (PH 7.3 7.35) & hypercapnia (PaCO2 45 60 mm of Hg) c) Resp. frequency > 25 breaths /min
Resp. frequency > 35 breaths /min Life threatening hypoxaemia: PaO2 (<40 mm of Hg)
(pH <7.25)
Severe acidosis
& hypercapnic
PaCO2 >60 mm
Resp. arrest Somnolence, impaired mental status. Hypotension, Shock, CHF Other complications (Sepsis, metabolic abnormalities, pneumonia, pulmonary embolism, massive pleural effusion) NIPPV failure
Conclusion
Cornerstones of management of
COPD exacerbation includes --
1. 2. 3. 4.
A timely intervention in acute exacerbation of COPD significantly reduces the morbidity & mortality.
Whats new
Experts believe that patients do best on "triple therapy," taking three different medications: a longacting beta-agonist, an inhaled corticosteroid, and the anticholinergic Spiriva (generic name tiotropium bromide). Pulmonary hypertension, or high blood pressure in the arteries leading to the lungs, is a common complication of COPD. The FDA has approved a new formulation of sildenafil called Revatio that's specifically for pulmonary hypertension.
Replacing oxygen with a mix of helium and oxygen. When 60 percent helium was combined with 40 percent oxygen -- making a mixture known as Heliox -- COPD patients were able to increase their exercise capacity by an average of 245 percent. Because helium is less dense than oxygen, it allows COPD sufferers to empty their damaged lungs more completely. Bronchoscopic surgery - Researchers are experimenting with using a bronchoscope-guided needle to create tiny holes through the airway walls. Miniature tubes called stents are then inserted to connect the smaller, collapsed airways with the healthier, bigger airways.
Roflumilast a new medication, (brand name Daxas) has been approved in Europe and USA for chronic bronchitis type ofCOPD. It targets PDE-4 and inhibits inflammation in COPD patients.
Key Points
COPD is preventable and treatable Encourage smokers to quit at every opportunity Dyspnea, cough, and sputum consider COPD Confirm with spirometry Four (4) components of COPD management Pharmacologic treatment Non-pharmacologic treatment Patient education is very important COPD often associated with exacerbations
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