MODULE 1 ยท GDFM PROGRAMME

Chronic Lung Diseases in Primary Care

๐Ÿ“… ๐Ÿ› College of Family Physicians Singapore

Learning Objectives

  • Understand the indications and interpretation of spirometry in primary care
  • Recognise and manage bronchiectasis and post-TB lung disease (PTLD)
  • Diagnose and manage asthma according to GINA 2024 guidelines
  • Diagnose and manage COPD using the GOLD 2024 ABE framework
  • Identify when to suspect interstitial lung disease (ILD) and initiate referral
  • Apply Singapore MOH ACE 2024 recommendations in clinical practice

Spirometry: Indications in Primary Care

  • Confirming diagnosis of asthma, COPD, or other lung disease
  • Monitoring disease progression and treatment response
  • Pre-operative assessment and occupational health screening
  • ๐Ÿ’Ž Spirometry is the gold standard โ€” PEF monitoring is an alternative if unavailable but is less reliable
  • Validity requires: โ‰ฅ3 technically acceptable manoeuvres, two largest FVC and FEVโ‚ within 150 mL of each other
  • Always perform post-bronchodilator testing when confirming COPD diagnosis
Example spirometry printout: FVC, FEV1, FEV1/FVC with flow-volume loops showing obstructive pattern

Example spirometry printout: FVC, FEV1, FEV1/FVC with flow-volume loops showing obstructive pattern

Lung Volumes & Capacities

  • Tidal Volume (TV): Normal breathing (~500 mL at rest)
  • Inspiratory Reserve Volume (IRV): Extra air inhaled beyond tidal breath
  • Expiratory Reserve Volume (ERV): Extra air exhaled beyond tidal breath
  • Residual Volume (RV): Air remaining after maximal exhalation โ€” NOT measured by spirometry
  • Functional Residual Capacity (FRC) = ERV + RV
  • Total Lung Capacity (TLC) = VC + RV โ€” requires body plethysmography
Diagram of lung volumes and capacities

Diagram of lung volumes and capacities

Flow-Volume Loops: Normal vs Obstructive vs Restrictive

  • Normal: smooth, triangular expiratory limb; symmetric inspiratory limb
  • Obstructive: concave (scooped out) expiratory limb โ€” classic in asthma and COPD
  • Restrictive: preserved shape but reduced volumes (smaller loop)
  • ๐Ÿ’Ž FEVโ‚/FVC < 0.70 (post-BD) = obstruction; FEVโ‚/FVC โ‰ฅ 0.70 with reduced FVC = restriction
  • Variable intrathoracic obstruction (e.g., tracheomalacia): expiratory limb flattened
  • Variable extrathoracic obstruction (e.g., vocal cord palsy): inspiratory limb flattened
Normal, obstructive, and restrictive flow-volume loop patterns

Normal, obstructive, and restrictive flow-volume loop patterns

Spirometry Interpretation Algorithm

  • Step 1: Assess FEVโ‚/FVC ratio โ€” is it < 0.70 (LLN)?
  • Step 2: If obstructive โ€” perform bronchodilator reversibility test
  • Step 3: If FEVโ‚/FVC โ‰ฅ 0.70 โ€” check if FVC is reduced โ†’ restrictive pattern
  • Step 4: Bronchodilator reversibility (โ‰ฅ12% and โ‰ฅ200 mL FEVโ‚ increase) suggests asthma
  • Step 5: Mixed pattern = obstruction + reduced FVC (e.g., severe COPD with air trapping)
  • ๐Ÿ’Ž Always interpret in clinical context โ€” spirometry alone does not make a diagnosis
Clinical algorithm for spirometry interpretation

Clinical algorithm for spirometry interpretation

Bronchodilator Reversibility Testing

  • Administer 200-400 mcg salbutamol via MDI + spacer
  • Withhold SABA โ‰ฅ4h, LABA 24-48h before test for diagnostic accuracy
  • Repeat spirometry 10-15 minutes after bronchodilator
  • Positive (adults): FEVโ‚ or FVC increase โ‰ฅ12% AND โ‰ฅ200 mL
  • Greater confidence: โ‰ฅ15% increase and โ‰ฅ400 mL
  • ๐Ÿ’Ž Positive reversibility suggests asthma but does NOT exclude COPD (or confirm ACO)

Bronchiectasis: Overview

  • Chronic irreversible airway dilatation from recurrent infection/inflammation
  • Presents with: persistent productive cough, purulent sputum, recurrent exacerbations
  • Common causes: post-infectious (TB, pertussis), immune deficiency, primary ciliary dyskinesia, CF
  • ๐Ÿ’Ž Post-TB bronchiectasis is a major cause in Singapore and SE Asia
  • Diagnosis: HRCT chest (shows dilated airways, 'signet ring' sign, mucus plugging)
  • Key complication: haemoptysis โ€” can be life-threatening
Treatable traits in bronchiectasis pathophysiology

Treatable traits in bronchiectasis pathophysiology

Bronchiectasis & PTLD: Management

  • Goals: reduce symptom burden, improve QoL, decrease exacerbations, prevent progression
  • Airway clearance: physiotherapy, huffing/coughing techniques, oscillating PEP devices
  • Long-term macrolides (azithromycin): reduces exacerbation frequency in RCTs
  • Inhaled antibiotics (e.g., tobramycin, colistin): for chronic Pseudomonas colonization
  • Vaccinations: pneumococcal + influenza (essential for all patients)
  • ๐Ÿ’Ž Pulmonary rehabilitation and smoking cessation are key for PTLD management

Asthma: Definition & Phenotypes (GINA 2024)

  • Heterogeneous disease with chronic airway inflammation
  • Defined by: variable respiratory symptoms (wheeze, SOB, chest tightness, cough) + variable expiratory airflow limitation
  • Allergic asthma: most common; childhood onset, atopy, eosinophilic, responds well to ICS
  • Non-allergic asthma: sputum neutrophilic/eosinophilic/paucigranulocytic
  • Adult-onset asthma: often non-allergic; rule out occupational asthma
  • Obesity-associated asthma: prominent symptoms, little eosinophilic inflammation

Asthma: Making the Diagnosis

  • Requires BOTH: (1) characteristic variable symptom pattern AND (2) confirmed variable airflow limitation
  • Symptoms: wheeze, SOB, chest tightness, cough โ€” vary over time and intensity
  • Often worse at night/morning; triggered by exercise, allergens, cold air, viral infections
  • Confirm with spirometry: positive BD reversibility (FEVโ‚ โ‰ฅ12% + โ‰ฅ200 mL) or PEF variability >10%/day
  • If initial tests negative โ€” repeat during symptoms or early morning
  • ๐Ÿ’Ž Do NOT start long-term treatment without objective evidence of variable airflow limitation

Asthma Diagnostic Criteria (GINA 2024)

  • Positive BD reversibility: FEVโ‚ โ‰ฅ12% + โ‰ฅ200 mL (adults); FEVโ‚ โ‰ฅ12% predicted (children)
  • PEF variability >10%/day (adults) or >13%/day (children) over 2 weeks
  • Increase in FEVโ‚ โ‰ฅ12% + โ‰ฅ200 mL after 4 weeks of ICS treatment
  • Positive methacholine challenge: FEVโ‚ fall โ‰ฅ20%
  • Variation in FEVโ‚ โ‰ฅ12% + โ‰ฅ200 mL between visits
  • ๐Ÿ’Ž The more tests are positive and the more often they are positive, the more confident the diagnosis

Asthma: Differential Diagnosis

  • Children 6-11: Upper airway cough syndrome, inhaled foreign body, bronchiectasis, CF, congenital heart disease
  • Adolescents/Adults: Inducible laryngeal obstruction (stridor, not wheeze), hyperventilation
  • All ages: COPD (older smokers), cardiac failure (orthopnoea, PND), ACE inhibitor cough
  • Constitutional symptoms (fever, night sweats, weight loss) โ†’ consider TB
  • ๐Ÿ’Ž Asthma-COPD Overlap (ACO) exists โ€” look for features of both
  • Comorbidities (rhinosinusitis, GERD, obesity, OSA) can coexist AND worsen asthma control

Asthma Assessment: Control & Severity

  • Two domains: (1) Symptom control over past 4 weeks; (2) Future risk of adverse outcomes
  • Symptom control: daytime symptoms, night waking, activity limitation, reliever use
  • ๐Ÿ’Ž Good symptom control does NOT mean no risk โ€” lung function and exacerbation history must be assessed
  • Severe asthma: uncontrolled despite high-dose ICS-LABA OR requiring it to stay controlled
  • Before diagnosing severe asthma: exclude poor technique, poor adherence, wrong diagnosis, comorbidities
  • Spirometry: at diagnosis, 3-6 months after starting treatment, then periodically
BREATHE mnemonic for asthma assessment (MOH Singapore)

BREATHE mnemonic for asthma assessment (MOH Singapore)

Asthma Control Test (ACT)

  • 5 questions covering activity limitation, shortness of breath, night symptoms, reliever use, overall control
  • Scored 1-5 for each question (max 25)
  • Score 20-25: Well-controlled asthma
  • Score 16-19: Not well-controlled asthma โ€” step up treatment
  • Score 5-15: Very poorly controlled asthma โ€” urgent review
  • ๐Ÿ’Ž Use ACT at every follow-up as a standardized objective measure of control
Asthma Control Test (ACT) questionnaire

Asthma Control Test (ACT) questionnaire

Asthma Medications: Key Terminology

  • Controller: ICS-containing medication for regular daily use (targets inflammation AND risk)
  • Reliever: As-needed inhaler for quick symptom relief (salbutamol, ICS-formoterol)
  • Anti-inflammatory Reliever (AIR): Low-dose ICS + rapid-acting BD (budesonide-formoterol)
  • MART (Maintenance-And-Reliever Therapy): ICS-formoterol for BOTH maintenance AND relief
  • ๐Ÿ’Ž Only specific ICS-formoterol combinations can be used as MART (NOT salmeterol, vilanterol etc.)
  • LTRA (e.g., montelukast): Alternative add-on controller; less effective than ICS for exacerbation prevention

ICS Dose Equivalencies (GINA 2024)

  • Low dose ICS: Budesonide 200-400 mcg/day; Beclometasone 200-500 mcg/day; Fluticasone propionate 100-250 mcg/day
  • Medium dose: Budesonide 400-800 mcg/day; Beclometasone 500-1000 mcg; Fluticasone prop 250-500 mcg
  • High dose: Budesonide >800 mcg/day; Beclometasone >1000 mcg; Fluticasone prop >500 mcg
  • Children (6-11 yr): doses approximately halved; always use lowest effective dose
  • Extrafine particle formulations (e.g., Qvar) achieve deeper lung deposition at lower doses
  • ๐Ÿ’Ž Doubling the ICS dose for exacerbations has limited evidence; ICS-formoterol MART is preferred strategy
ICS dose equivalency table โ€” adults/adolescents and children

ICS dose equivalency table โ€” adults/adolescents and children

GINA 2024: Two-Track Treatment Approach

  • Track 1 (Preferred): As-needed low-dose ICS-formoterol as reliever AT ALL STEPS
  • Track 2 (Alternative): As-needed SABA reliever + separate daily controller
  • ๐Ÿšจ SABA-only treatment (no ICS) is NO LONGER recommended โ€” associated with increased exacerbation risk and death
  • Track 1 advantage: every reliever puff delivers anti-inflammatory protection
  • MART strategy: budesonide-formoterol OR beclometasone-formoterol for maintenance AND relief
  • ๐Ÿ’Ž Track 1 reduces severe exacerbations by ~60-70% compared to SABA-only in clinical trials
GINA 2024 two-track initial asthma treatment flowchart

GINA 2024 two-track initial asthma treatment flowchart

Stepwise Asthma Treatment (Adults โ‰ฅ12 years)

  • Step 1: As-needed low-dose ICS-formoterol (Track 1) OR low-dose ICS when SABA taken (Track 2)
  • Step 2: As-needed low-dose ICS-formoterol (Track 1) OR daily low-dose ICS + as-needed SABA
  • Step 3: Low-dose ICS-formoterol MART (Track 1) OR daily low-dose ICS-LABA + SABA
  • Step 4: Medium-dose ICS-formoterol MART (Track 1) OR medium/high-dose ICS-LABA + SABA
  • Step 5: High-dose ICS-LABA ยฑ LAMA; investigate severe asthma; consider biologics
  • ๐Ÿ’Ž Step up if uncontrolled for โ‰ฅ3 months (after checking technique, adherence, triggers)
MOH Singapore ACE stepwise pharmacological treatment for asthma

MOH Singapore ACE stepwise pharmacological treatment for asthma

GINA 2024 Management Cycle

  • Cycle: Assess โ†’ Adjust treatment โ†’ Review response
  • Assess: symptom control, risk factors, inhaler technique, adherence, comorbidities
  • Adjust: step up or down based on response; address modifiable risk factors
  • Review: 1-3 months after starting/changing treatment; 3-6 monthly in stable patients
  • Non-pharmacological: smoking cessation, allergen avoidance, exercise, obesity management
  • ๐Ÿ’Ž Personalise treatment โ€” consider patient preferences, cost, device availability
GINA 2024 Assess-Start-Review management cycle

GINA 2024 Assess-Start-Review management cycle

Inhaler Technique: Pearls

  • Poor inhaler technique is a leading cause of uncontrolled asthma
  • MDI: shake โ†’ breathe out fully โ†’ slow deep breath in while pressing โ†’ hold 10 sec
  • DPI (Turbuhaler/Accuhaler): fast forceful inhalation required; do NOT exhale into device
  • Spacer: increases lung deposition from MDI by 2-3x; essential for children and patients with poor coordination
  • ๐Ÿ’Ž Always demonstrate technique AND ask patient to show you back ('teach-back')
  • Reassess technique at EVERY consultation โ€” errors recur even after correct initial training

Written Asthma Action Plan (WAAP)

  • Essential for all patients โ€” reduces emergency visits and hospitalisations
  • Three zones: Green (controlled), Yellow (worsening), Red (emergency)
  • Green: continue regular medications as prescribed
  • Yellow: increase reliever, start/increase preventer, consider OCS if not improving in 24-48h
  • Red: call ambulance / go to A&E immediately if too breathless to speak
  • ๐Ÿ’Ž Personalise to patient's medications; review and update at every visit
Written Asthma Action Plan (WAAP) example with traffic light zones

Written Asthma Action Plan (WAAP) example with traffic light zones

Preventer Medications in Singapore

  • ICS alone: Budesonide (Pulmicort), Fluticasone propionate (Flixotide), Beclometasone (Qvar)
  • ICS-LABA combinations: Budesonide-formoterol (Symbicort/Pulmicort Turbuhaler), Fluticasone-salmeterol (Seretide), Fluticasone-vilanterol (Relvar)
  • LAMA add-on (Step 5): Tiotropium (Spiriva Respimat) โ€” for adult asthma
  • Biologics (severe asthma, Step 5): Omalizumab (anti-IgE), Dupilumab (anti-IL-4/13), Benralizumab (anti-IL-5Rฮฑ)
  • LTRA: Montelukast โ€” adjunct, less effective for exacerbation prevention than ICS
  • ๐Ÿ’Ž For MART: Only budesonide-formoterol or beclometasone-formoterol are approved
Preventer medications for asthma registered in Singapore (MOH ACE 2020)

Preventer medications for asthma registered in Singapore (MOH ACE 2020)

Acute Asthma: Severity Classification

๐Ÿšจ Emergency โ€” Act Now
๐Ÿšจ
  • Mild: dyspnoea only with activity; PEF/FEVโ‚ >70% predicted/personal best
  • Moderate: dyspnoea limits usual activity; PEF/FEVโ‚ 40-69%
  • Severe: dyspnoea at rest; interferes with conversation; PEF/FEVโ‚ <40%
  • Life-threatening: too dyspnoeic to speak; perspiring, drowsy, confused; PEF/FEVโ‚ <25%
  • ๐Ÿšจ Life-threatening features: silent chest, cyanosis, poor respiratory effort, altered consciousness โ†’ IMMEDIATE ambulance transfer
  • ๐Ÿ’Ž Document initial SpOโ‚‚ and PEF/FEVโ‚ โ€” essential for severity grading and monitoring response

Acute Asthma: Primary Care Management

๐Ÿšจ Emergency โ€” Act Now
๐Ÿšจ
  • Mild-Moderate: Salbutamol 4-8 puffs via MDI+spacer q20min ร— 3; SpOโ‚‚ target โ‰ฅ95%; reassess in 1h
  • Severe: Salbutamol + ipratropium bromide q20min ร— 3; Prednisolone 40-50 mg orally; Oxygen to SpOโ‚‚ โ‰ฅ95%
  • No response or deterioration โ†’ CALL AMBULANCE; continue bronchodilators while awaiting
  • ๐Ÿšจ IV magnesium sulphate 2g over 20 min if no response in secondary care
  • Discharge criteria (mild-moderate): PEF/FEVโ‚ >60-70%, symptoms resolved, able to self-manage
  • All patients after exacerbation: review within 2-7 days; update WAAP; check inhaler technique

Acute Asthma: ED Management

๐Ÿšจ Emergency โ€” Act Now
๐Ÿšจ
  • Initial rapid assessment: vital signs, SpOโ‚‚, PEF/FEVโ‚, clinical severity
  • Immediate: oxygen (SpOโ‚‚ โ‰ฅ95%), salbutamol + ipratropium nebs q20min, systemic corticosteroids
  • Severe: IV magnesium sulphate 2g over 20 min (reduces hospitalisation risk)
  • Reassess 1h: good response (PEF >60%) โ†’ may discharge with close follow-up
  • Poor response or life-threatening โ†’ ICU; consider IV salbutamol, intubation as last resort
  • ๐Ÿšจ Avoid sedatives/opioids in acute asthma โ€” suppress respiratory drive

Asthma in Children โ‰ค5 Years: Diagnosis

  • Challenging โ€” episodic wheeze and cough common in this age group
  • More likely asthma if: recurrent symptoms, worse at night, triggered by exercise/allergens/viral URTI
  • Trial of treatment: response to short-term low-dose ICS supports diagnosis
  • Differential: recurrent viral wheeze (no atopy, well between episodes), GERD, foreign body, pertussis, bronchiectasis
  • ๐Ÿ’Ž Consider referral to paediatrician if: <1 year old, atypical symptoms, poor treatment response
  • Do NOT use peak flow meters in children <5 years (cannot reliably perform manoeuvre)

Asthma in Children โ‰ค5 Years: Management

  • Reliever: Salbutamol 200-400 mcg via MDI+spacer (with mask if <4 years) q20min for acute episodes
  • Step 1: As-needed SABA only for infrequent wheeze
  • Step 2: Daily low-dose ICS (budesonide 200 mcg/day) OR daily montelukast if ICS not feasible
  • Step 3: Increase ICS dose OR add montelukast; consider specialist referral
  • Step 4: Specialist referral for further evaluation and management
  • ๐Ÿ’Ž MDI + spacer + face mask is the preferred delivery device for children under 4 years

Paediatric Inhaler Technique & ICS Dosing

  • Always use spacer with MDI for children โ€” face mask for <4 years, mouthpiece for โ‰ฅ4 years
  • Low-dose ICS in children: Budesonide 100-200 mcg/day; BDP 100-200 mcg; FP 50-100 mcg
  • Wash and air-dry spacer weekly โ€” detergent reduces electrostatic charge improving drug delivery
  • Counsel parents: ICS at appropriate doses do NOT stunt growth significantly when benefits outweigh risks
  • ๐Ÿ’Ž Demonstrate pMDI + spacer + mask technique to both parent AND child at every visit
  • Video resources: National Asthma Council Australia website has age-specific inhaler technique guides

COPD: Definition & Risk Factors

  • Heterogeneous lung condition โ€” persistent airflow obstruction from airway (bronchitis/bronchiolitis) and/or alveolar (emphysema) abnormalities
  • Key symptoms: chronic dyspnoea (especially exertional), cough, sputum production
  • Leading global cause of morbidity and mortality; often underdiagnosed
  • Risk factors: TOBACCO SMOKE (most important), household/outdoor air pollution, occupational dusts/chemicals
  • Alpha-1-antitrypsin deficiency: rare genetic cause โ€” suspect in non-smokers or early-onset COPD
  • Early life events: prematurity, low birth weight, childhood respiratory infections also contribute

COPD: Diagnosis (GOLD 2024)

  • ALL THREE required: (1) typical symptoms + (2) risk factor exposure + (3) spirometry confirmation
  • Spirometry: Post-bronchodilator FEVโ‚/FVC < 0.70 confirms airflow obstruction
  • Do NOT diagnose COPD without spirometry โ€” clinical features alone are insufficient
  • ๐Ÿ’Ž Spirometry is essential: many patients have 'silent' disease until spirometry reveals significant obstruction
  • Exclude other diagnoses: asthma, cardiac failure, bronchiectasis, TB
  • Screen proactively: any patient >35 years with smoking history AND symptoms
Spirometry in COPD: obstructive pattern (FEV1/FVC = 0.56)

Spirometry in COPD: obstructive pattern (FEV1/FVC = 0.56)

COPD vs Asthma: Key Differences

  • COPD: usually โ‰ฅ40 years; persistent/progressive dyspnoea; significant smoking/exposure history
  • Asthma: any age; variable episodic symptoms; personal/family history of atopy; triggers
  • COPD: persistent post-BD obstruction (FEVโ‚/FVC <0.70); minimal reversibility
  • Asthma: often normal lung function between episodes; significant reversibility (โ‰ฅ12% + โ‰ฅ200 mL)
  • ๐Ÿ’Ž Asthma-COPD Overlap (ACO): features of both; eosinophilia + BD reversibility; treat with ICS + LABD
  • Chest X-ray: COPD may show hyperinflation, flat diaphragms; asthma usually normal

COPD Assessment Tools: mMRC & CAT

  • mMRC Grade 0: Breathless only with strenuous exercise
  • mMRC Grade 1: Short of breath when hurrying or walking up a slight hill
  • mMRC Grade 2: Walks slower than others due to breathlessness, or stops to rest
  • mMRC Grade 3: Stops for breath after ~100m on flat ground
  • mMRC Grade 4: Too breathless to leave house; breathless when dressing/undressing
  • ๐Ÿ’Ž CAT score โ‰ฅ10 = significant symptom burden; use CAT for more comprehensive assessment

GOLD ABE Classification (Current Standard)

  • Replaced the old ABCD tool from 2023 โ€” spirometry severity (GOLD 1-4) no longer drives initial therapy choice
  • Group A: Low symptoms (mMRC 0-1 OR CAT <10) AND 0-1 moderate exacerbations (not hospitalised)
  • Group B: High symptoms (mMRC โ‰ฅ2 OR CAT โ‰ฅ10) AND 0-1 moderate exacerbations
  • Group E: โ‰ฅ2 moderate exacerbations OR โ‰ฅ1 severe exacerbation (hospitalisation in past year)
  • ๐Ÿ’Ž Exacerbation history is the single best predictor of future exacerbations โ€” ask at EVERY visit
  • Still measure FEVโ‚ for grading severity (GOLD 1-4) and guiding some add-on therapy decisions
GOLD 2023+ ABE assessment framework

GOLD 2023+ ABE assessment framework

COPD Clinical Phenotypes

  • ACO (Asthma-COPD Overlap): High eosinophils, BD reversibility โ€” ICS is essential
  • Frequent Exacerbator: โ‰ฅ2 moderate or โ‰ฅ1 severe/year โ€” LABA+LAMA ยฑ ICS; consider roflumilast/azithromycin
  • Emphysema-predominant: CT emphysema, hyperinflation, low BMI โ€” consider lung volume reduction
  • Chronic Bronchitis: Productive cough โ‰ฅ3 months ร— 2 years โ€” mucolytics, roflumilast
  • Physical Frailty (gait speed <0.8 m/s): Pulmonary rehab with strength training
  • ๐Ÿ’Ž Identify predominant phenotype to guide personalised management beyond ABE grouping

COPD Management Cycle

  • Diagnose โ†’ Initial assessment (ABE group, symptoms, comorbidities) โ†’ Implement initial management
  • Review: symptom control, exacerbation frequency, side effects, inhaler technique
  • Adjust: escalate or de-escalate pharmacotherapy; add non-pharmacological interventions
  • ๐Ÿ’Ž Reassess blood eosinophil count to guide ICS use โ€” high eosinophils (โ‰ฅ300) favour ICS
  • Check: inhaler technique and adherence at EVERY visit
  • Address comorbidities: cardiovascular disease, depression, osteoporosis, lung cancer screening
GOLD COPD management cycle diagram

GOLD COPD management cycle diagram

COPD: Initial Pharmacotherapy (GOLD ABE)

  • Group A: ONE long-acting bronchodilator โ€” LAMA (preferred) or LABA
  • Group B: DUAL bronchodilator โ€” LAMA + LABA (superior to monotherapy for symptom relief)
  • Group E: LAMA + LABA; if eosinophils โ‰ฅ300 cells/ฮผL โ†’ start LAMA + LABA + ICS (triple therapy)
  • ๐Ÿ’Ž ICS should NOT be used as initial monotherapy in COPD โ€” only appropriate in triple therapy or ACO
  • All patients: short-acting bronchodilator (SABA or SAMA) for breakthrough symptoms
  • Reassess at 3 months for symptom response and exacerbation reduction
GOLD 2024 initial pharmacotherapy by ABE group

GOLD 2024 initial pharmacotherapy by ABE group

COPD: Follow-up Pharmacotherapy Algorithm

  • Persistent DYSPNOEA on monotherapy โ†’ escalate to LAMA+LABA; if already on dual โ†’ check technique/switch
  • Persistent EXACERBATIONS on LAMA+LABA: check blood eosinophils to guide next step
  • Eosinophils โ‰ฅ300: add ICS โ†’ triple therapy (LAMA+LABA+ICS)
  • Eosinophils 100-300: consider adding ICS if still exacerbating
  • Eosinophils <100: ICS unlikely effective; consider ROFLUMILAST (FEVโ‚ <50%, chronic bronchitis) or AZITHROMYCIN (ex-smokers)
  • ๐Ÿ’Ž ICS overuse increases risk of pneumonia in COPD โ€” reserve for those with high eosinophils or frequent exacerbations
COPD follow-up pharmacotherapy algorithm โ€” dyspnoea vs exacerbation pathway

COPD follow-up pharmacotherapy algorithm โ€” dyspnoea vs exacerbation pathway

COPD: Non-Pharmacological Management

  • ๐Ÿšจ SMOKING CESSATION: single most effective intervention โ€” slows FEVโ‚ decline, reduces mortality
  • Vaccinations: Influenza (annual), Pneumococcal (PCV20 or PCV13+PPSV23), COVID-19, Tdap, RSV
  • Pulmonary Rehabilitation (PR): essential for Group B and E โ€” improves dyspnoea, exercise capacity, QoL
  • Physical Activity: encourage daily walking; even moderate activity improves outcomes
  • Long-Term Oxygen Therapy (LTOT): indicated if PaOโ‚‚ โ‰ค55 mmHg or SaOโ‚‚ โ‰ค88% at rest โ€” improves survival
  • ๐Ÿ’Ž Palliative care referral early: severe COPD has a poor prognosis; advance care planning is essential
Non-pharmacological COPD management by patient group (GOLD 2024)

Non-pharmacological COPD management by patient group (GOLD 2024)

๐Ÿšจ COPD Exacerbations: Classification & Management

  • Mild: treat with SABDs (SABA ยฑ SAMA) alone; no antibiotic or OCS required
  • Moderate: SABDs + antibiotics AND/OR oral corticosteroids (prednisolone 40 mg ร— 5 days)
  • Severe: hospitalisation required; IV bronchodilators, controlled oxygen (SpOโ‚‚ 88-92%), NIV
  • Antibiotics indicated if: increased dyspnoea + increased sputum volume + increased purulence (all 3 cardinal signs)
  • ๐Ÿšจ NIV is first-line for hypercapnic respiratory failure in COPD โ€” reduces intubation and mortality
  • ๐Ÿ’Ž Post-exacerbation: review within 4 weeks; optimise maintenance therapy; cardiac cause?
COPD exacerbation severity algorithm and differential diagnosis

COPD exacerbation severity algorithm and differential diagnosis

Singapore MOH ACE: COPD Diagnosis (2024)

  • Suspect COPD: any patient โ‰ฅ40 years with dyspnoea, chronic cough/sputum, and risk factor exposure
  • Confirm with post-bronchodilator spirometry: FEVโ‚/FVC < 0.70
  • Assess: symptoms (CAT/mMRC), exacerbation history, blood eosinophil count
  • Exclude: asthma, cardiac failure, bronchiectasis, TB
  • Refer if: uncertain diagnosis, rapid decline, severe disease (FEVโ‚ <30%), suspected lung cancer
  • ๐Ÿ’Ž Many COPD patients in Singapore are underdiagnosed โ€” proactive case-finding in at-risk individuals is recommended
Singapore MOH ACE COPD diagnostic algorithm (June 2024)

Singapore MOH ACE COPD diagnostic algorithm (June 2024)

Singapore MOH ACE: COPD Management (2024)

  • Strong recommendation: smoking cessation counselling at every visit
  • Dual LABD (LAMA+LABA) preferred for patients with significant symptoms or exacerbation risk
  • Triple therapy (LAMA+LABA+ICS) for frequent exacerbators with eosinophils โ‰ฅ300 cells/ฮผL
  • Assess inhaler technique and adherence at every visit โ€” use the 'show me how' approach
  • Refer for pulmonary rehabilitation: for Group B and E patients
  • ๐Ÿ’Ž ICS de-escalation: consider withdrawing ICS if eosinophils <100 and not exacerbating โ€” reduces pneumonia risk
Singapore MOH ACE COPD management flowchart (June 2024)

Singapore MOH ACE COPD management flowchart (June 2024)

COPD Inhalers Available in Singapore

  • SABA: Salbutamol (Ventolin), Terbutaline (Bricanyl) โ€” short-acting, for rescue
  • SAMA: Ipratropium (Atrovent) โ€” short-acting antimuscarinic, useful in acute exacerbations
  • LAMA: Tiotropium (Spiriva HandiHaler/Respimat), Umeclidinium (Incruse), Glycopyrronium (Seebri)
  • LAMA+LABA: Umeclidinium-vilanterol (Anoro), Tiotropium-olodaterol (Spiolto), Glycopyrronium-formoterol (Bevespi)
  • LABA+ICS or LAMA+LABA+ICS: e.g., Fluticasone-salmeterol (Seretide), Fluticasone furoate-vilanterol-umeclidinium (Trelegy)
  • ๐Ÿ’Ž Do NOT combine two inhalers from the same drug class (e.g., two LAMAs) โ€” no added benefit, increased risk

COPD: Comorbidities

  • Cardiovascular disease: most common comorbidity; increases mortality independently
  • ๐Ÿ’Ž Beta-blockers are NOT contraindicated in COPD โ€” use for appropriate cardiac indications (heart failure, post-MI)
  • Lung cancer: 4-6x increased risk in COPD; low-dose CT screening for heavy smokers (โ‰ฅ30 pack-years, โ‰ฅ50 years)
  • Osteoporosis: screen and treat; ICS and smoking both increase fracture risk
  • Depression and anxiety: highly prevalent; screen with PHQ-2 and GAD-2; treat if positive
  • GERD: common; can trigger exacerbations; treat symptomatically

Interstitial Lung Disease (ILD): Overview

  • Large, heterogeneous group of conditions โ€” inflammation and/or fibrosis of lung interstitium
  • Impaired gas exchange โ†’ progressive dyspnoea, dry cough, fatigue, chest discomfort
  • Restrictive physiology on PFTs: reduced TLC, FVC; normal or elevated FEVโ‚/FVC ratio
  • Key categories: idiopathic (IPF), autoimmune-related, exposure-related, sarcoidosis, others
  • Epidemiology: IPF incidence increasing; prognosis poor (median survival ~3-5 years from diagnosis)
  • ๐Ÿ’Ž ILD is often underdiagnosed โ€” progressive unexplained dyspnoea with bibasilar crackles should prompt investigation
Classification of interstitial lung diseases

Classification of interstitial lung diseases

IPF: Pathophysiology

  • Idiopathic Pulmonary Fibrosis (IPF): most common idiopathic IIP; progressive, irreversible fibrosis
  • Repeated microinjuries to alveolar epithelium โ†’ abnormal wound healing โ†’ fibroblast activation โ†’ fibrosis
  • Gross: honeycombing (subpleural, basal-predominant) on HRCT
  • Loss of gas exchange surface โ†’ hypoxaemia, especially on exertion
  • Risk factors: male sex, older age (>60), cigarette smoking, environmental exposures
  • ๐Ÿ’Ž IPF has no truly effective cure โ€” anti-fibrotics slow progression but do not reverse fibrosis
Healthy lung vs IPF: alveolar fibrosis and gas exchange impairment

Healthy lung vs IPF: alveolar fibrosis and gas exchange impairment

When to Suspect ILD: Primary Care Red Flags

  • Persistent unexplained DRY COUGH โ€” not productive, not responding to common treatments
  • Progressive EXERTIONAL DYSPNOEA โ€” insidious onset, worsening over months/years
  • Fine inspiratory VELCRO-LIKE CRACKLES at lung bases โ€” highly characteristic of fibrotic ILD
  • Finger clubbing โ€” present in ~50% of IPF cases; not seen in sarcoidosis
  • ๐Ÿ’Ž Take thorough exposure history: birds, mold, feather pillows, organic dusts, silica, asbestos exposure
  • Systemic features (joint pain, rash, Raynaud's, myalgia) suggest connective tissue disease-associated ILD

ILD: Initial Investigations & Referral

  • Chest X-ray: reticular/nodular opacities, lower zone predominance; can be NORMAL in early disease
  • Spirometry: restrictive pattern (reduced FVC, normal or elevated FEVโ‚/FVC; reduced TLC on plethysmography)
  • Reduced DLCO (diffusing capacity): sensitive early indicator of gas exchange impairment
  • Blood tests: FBC, ESR, CRP, ANA, anti-dsDNA, anti-Scl70, anti-Ro/La, RF โ€” screen for connective tissue disease
  • ๐Ÿšจ REFER to respiratory specialist for HRCT chest + MDT discussion โ€” do NOT delay referral
  • ๐Ÿ’Ž Do NOT start empirical immunosuppression in primary care โ€” accurate diagnosis essential before treatment

ILD: HRCT Patterns

  • UIP (Usual Interstitial Pneumonia): subpleural, basal honeycombing ยฑ traction bronchiectasis โ†’ IPF
  • NSIP (Non-Specific Interstitial Pneumonia): bilateral ground glass ยฑ reticulation; autoimmune-related
  • Hypersensitivity Pneumonitis: centrilobular nodules, ground glass, mosaic attenuation
  • Sarcoidosis: perilymphatic nodules, hilar/mediastinal lymphadenopathy
  • Organising Pneumonia: consolidation, often peribronchial or subpleural โ€” can mimic pneumonia
  • ๐Ÿ’Ž HRCT pattern guides MDT diagnosis and determines management approach
CT patterns in ILDs: IPF, NSIP, HP, sarcoidosis, organising pneumonia

CT patterns in ILDs: IPF, NSIP, HP, sarcoidosis, organising pneumonia

ILD: Management Principles

  • Gold standard: MDT evaluation (pulmonologist, radiologist, pathologist) โ€” improves diagnostic accuracy
  • Anti-fibrotics (IPF): Pirfenidone or Nintedanib โ€” slows FVC decline by ~50%; does not reverse fibrosis
  • Immunosuppression (connective tissue disease-ILD, HP): corticosteroids ยฑ steroid-sparing agents
  • Remove exposure: critical for hypersensitivity pneumonitis โ€” identify and eliminate causative antigen
  • Non-pharmacological: Pulmonary rehabilitation; supplemental oxygen for hypoxaemia; handheld fan for breathlessness
  • ๐Ÿ’Ž Advance care planning: integrate palliative care early; IPF is progressive and often fatal

Key Summary: Spirometry & Bronchiectasis

Key Point
๐Ÿ’Ž Spirometry is essential for diagnosing and monitoring obstructive and restrictive lung disease
Key Point
FEVโ‚/FVC <0.70 (post-BD) = obstruction; reduced FVC with normal ratio = restriction
Key Point
Positive BD reversibility (โ‰ฅ12% + โ‰ฅ200 mL) suggests asthma but does not exclude COPD
Key Point
Bronchiectasis: irreversible airway dilatation; manage with airway clearance, macrolides, vaccinations
Key Point
Post-TB lung disease is a major cause of morbidity in Singapore โ€” proactive management needed
Key Point
Spirometry is indicated for any patient with unexplained dyspnoea, chronic cough, or respiratory risk factors

Key Summary: Asthma

Key Point
Diagnosis requires BOTH variable symptoms AND confirmed variable airflow limitation โ€” do not treat empirically without evidence
Key Point
๐Ÿ’Ž GINA 2024 strongly prefers Track 1: ICS-formoterol as reliever at ALL steps โ€” reduces severe exacerbations by ~60-70%
Key Point
๐Ÿšจ SABA-only treatment is no longer recommended โ€” every patient should have an ICS-containing controller
Key Point
MART (budesonide-formoterol or beclometasone-formoterol): maintenance AND reliever in one inhaler
Key Point
Check inhaler technique and adherence at EVERY visit โ€” poor technique is the most common cause of poor control
Key Point
All patients should have a Written Asthma Action Plan (WAAP)

Key Summary: COPD

Key Point
Diagnosis requires symptoms + risk factor exposure + post-BD FEVโ‚/FVC <0.70 โ€” never diagnose without spirometry
Key Point
GOLD ABE framework (not ABCD): Group A โ†’ 1 LABD; Group B โ†’ LAMA+LABA; Group E โ†’ LAMA+LABA ยฑ ICS
Key Point
Blood eosinophil count guides ICS use: โ‰ฅ300 โ†’ add ICS; <100 โ†’ ICS unlikely effective
Key Point
๐Ÿ’Ž Smoking cessation is the MOST effective intervention โ€” reduces FEVโ‚ decline rate
Key Point
Vaccinations, pulmonary rehabilitation, and physical activity are essential non-pharmacological pillars
Key Point
๐Ÿšจ COPD exacerbation: SABDs + OCS (5 days) + antibiotics if all 3 cardinal signs present

Key Summary: ILD

Key Point
Suspect ILD in: progressive exertional dyspnoea + dry cough + bibasilar velcro crackles
Key Point
Restrictive spirometry + reduced DLCO โ†’ refer for HRCT and respiratory specialist MDT evaluation
Key Point
๐Ÿ’Ž Do NOT start empirical treatment in primary care โ€” accurate diagnosis via MDT is essential
Key Point
IPF: anti-fibrotics (pirfenidone/nintedanib) slow progression; no cure
Key Point
Connective tissue disease-ILD: immunosuppression; Hypersensitivity pneumonitis: remove causative antigen
Key Point
Integrate palliative care early โ€” progressive ILD has significant symptom burden and poor prognosis

References