Pulmonary Clinical Suitev2.0

GOLD 2025/2026 & GINA Guidelines Decision Engine
πŸŽ™οΈ Ambient Voice Scribe (In-Browser β€’ Zero Cloud Transmission)
πŸ“± iPhone / Mobile Voice Tip: Tap the box below and tap the πŸŽ™οΈ microphone icon on your iPhone keyboard (bottom right) to speak. When finished, tap ✨ Parse & Sync to auto-fill the algorithm.
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πŸ›οΈ Athena EHR & Prior VistA Fax Baseline Intake
Glance at your faxed VistA PDF in Athena's Document Tray and confirm baseline historical diagnostics below (zero patient name or MRN needed):
πŸ“ Active Problems to Pull into Unified Note:
1 Active
πŸ”€ Layout Approach:
Selections Made:
1 Treatment Status
START HERE
πŸ’Š Current Maintenance Inhalers (Select up to 3) Trelegy Ellipta (Triple)
SABA OVERUSE ⚠️
⚠️ Beta-Agonist Reliance Flag: Using SABA β‰₯2–3 days/week down-regulates ββ‚‚-receptors and increases acute exacerbation risk. Verify inhaler technique and prioritize daily maintenance controller.
↓
2 Airflow Severity (Post-BD FEV₁)
FEV₁/FVC < 0.70
↓
3 Symptom Burden (mMRC / CAT)
↓
4 Exacerbations & Blood Eosinophils
↓
5 Phenotypes, Smoking & Traits
Active Modifiers
🚬 Smoking History & LCS (USPSTF) Non-Screened
Total Burden: 30 Pack-Years 🎯 USPSTF LDCT Indicated
GOLD Grade 2 β€’ Group B
FEV₁ 50–79% β€’ BEC < 100 cells/Β΅L
GROUP B
πŸ’Š Inhaler Regimen
GOLD Evidence A
Dual LABA + LAMA Backbone
β€’ Umeclidinium / Vilanterol 62.5/25 mcg DPI QD
β€’ Tiotropium / Olodaterol 5/5 mcg SMI QD
β€’ Glycopyrrolate / Formoterol 18/9.6 mcg MDI BID
🚨 Acute COPD Exacerbation (Flare-Up)?
Open dedicated AECOPD Flare Tab for REDUCE 5-day steroid vs 12-day taper, Anthonisen antibiotics & BiPAP
⚑ Trait Escalation Pathways
Persistent Breathlessness:
1. Add Inhaled Ensifentrine 3 mg BID nebulized.
2. Pulmonary Rehabilitation (Evidence A).
3. Screen for Endobronchial Valves (BLVR) if severe hyperinflation.
1. Spirometry: GOLD Grade 2
2. Staging: Group B
3. Backbone: Dual LABA + LAMA
πŸ”€ Layout Approach:
Selections Made:
1 Treatment Track & Phase
↓
2 Daytime Symptoms & Night Waking
↓
3 Exacerbations & Biomarkers
↓
4 Phenotypes & Allergy Profiling
Active Modifiers
Track 1 MART β€’ GINA Step 1–2
Low-Dose ICS-Formoterol Reliever Alone
Step 1–2
🩺 Inhaler Regimen
GINA Evidence A
As-Needed Low-Dose ICS-Formoterol (Step 1–2)
β€’ Budesonide / Formoterol 160/4.5 mcg DPI: 1 inhalation PRN for relief. No daily controller.
🧬 Precision Biologic Selection
Matched to Patient
πŸ“‹ View Alternative / Other Biologics for Consideration β–Ύ
1. Strategy: Track 1 MART
2. Staging: GINA Step 1–2
AECOPD Protocol β€’ REDUCE 5-Day Steroid + Anthonisen Abx
Prednisone 40 mg PO daily x 5d β€’ DuoNeb QID β€’ Target SpOβ‚‚ 88–92%
ACUTE FLARE
1 Corticosteroid Regimen
2 Anthonisen Cardinal Symptoms & Antibiotics
3 Respiratory Support & Acuity
πŸ“‹ Generated AECOPD Flare Plan
Idiopathic Pulmonary Fibrosis (IPF) β€’ Ofev (Nintedanib)
150 mg PO BID with food
IPF ANTIFIBROTIC
1 Interstitial Lung Disease Subtype
2 Pharmacotherapy & Titration Protocol
πŸ“‹ Generated ILD / IPF Assessment & Plan
Mycobacterium Avium Complex (MAC) β€’ 3x/Week Regimen
Azithromycin 500mg + Ethambutol 1200mg + Rifampin 600mg TIW x 18 mo
MAC / NTM
1 Select Infectious / Mycobacterial Protocol
Auto-calculates Rifampin (10mg/kg), INH (10mg/kg), PZA (30mg/kg), Ethambutol (15mg/kg)
πŸ“‹ Generated Mycobacterial / Fungal Plan
WHO Group 1 Pulmonary Arterial Hypertension (PAH)
Upfront Ambrisentan + Tadalafil β€’ Consider Add-On Sotatercept
PULM HTN
1 Select Pulmonary Hypertension Pathway
πŸ“‹ Generated Pulmonary Hypertension Plan
Alpha-1 Antitrypsin Deficiency (AATD) β€’ Pi*ZZ Severe Deficiency
Serum AAT < 11 Β΅mol/L (<57 mg/dL) β€’ Prolastin-C 60 mg/kg IV Weekly
ALPHA-1 (AATD)
1 Alpha-1 Genotype & Clinical Scenario
πŸ“‹ Generated Alpha-1 Antitrypsin Plan
Smoking Cessation Protocol β€’ ATS 2020 & USPSTF Guideline Standard
First-Line Varenicline (Chantix) OR Combination NRT β€’ 5 A's Counseling β€’ CPT 99406 / 99407
Active Smoker
1 Tobacco & Nicotine Product Profile
Cigarettes Per Day:
Years Smoked:
Calculated Exposure: 30.0 Pack-Years
🎯 USPSTF Criteria Met: β‰₯ 20 Pack-Years. Eligible for Annual Low-Dose CT (LDCT) Lung Cancer Screening if age 50–80.
2 Readiness to Quit & Target Quit Date (5 A's Model)
3 Comorbidities & Pharmacotherapy Safety Screen
πŸ’Š Guideline-Recommended Pharmacotherapy (ATS 2020 & USPSTF)
πŸ—£οΈ Evidence-Based Behavioral Counseling Protocol
πŸ“‹ Athena / EMR Tobacco Cessation Note (CPT 99406 / 99407)
Master Pulmonary Medication Formulary & Trial Dosing Audit
Common Clinic Doses Verified Against Landmark Evidence β€’ Trial-Discrepant Dosing Highlighted
Formulary Audit
Drug Class Brand & Molecule Common Clinic Dosing (Formulary) Landmark Trial Protocol & Evidence Evidence Concordance Status
Systemic Steroid (AECOPD) Prednisone Oral Tablet
Acute COPD Flare Protocol
⚠️ Common 12-Day Taper (#30 tabs 10mg):
β€’ 40 mg daily x 3 days
β€’ 30 mg daily x 3 days
β€’ 20 mg daily x 3 days
β€’ 10 mg daily x 3 days (Total: 300 mg)
REDUCE Trial (JAMA 2013; PMID 23695200 β†—):
Prednisone 40 mg PO daily for 5 DAYS MAX (Total: 200 mg) was strictly non-inferior to 14 days (HR 0.95). Prolonged courses deliver zero relapse benefit and significantly increase infection, hyperglycemia, and adverse events.
⚠️ TRIAL DISCREPANT
GOLD 2025/2026 mandates 5 days max. Avoid unnecessary 12-day tapers.
Mucolytic Agent N-Acetylcysteine (NAC)
Oral Capsule
⚠️ Low-Dose / OTC Regimen:
600 mg PO Once Daily or 500 mg OTC daily
PANTHEON Trial (Lancet RM 2014; PMID 24621680 β†—):
High-Dose NAC 600 mg PO BID (1200 mg/day total) is mandatory for clinical efficacy; reduced annual exacerbations by 22% (NNT 7.4). Low-dose 600 mg/day showed no significant exacerbation benefit in BRONCUS trial.
⚠️ DOSE DISCREPANT
Must prescribe 600 mg BID (1200 mg/d) to match Phase 3 evidence.
Single-Inhaler Triple (DPI) Trelegy Ellipta
FF/UMEC/VI
100/62.5/25 mcg 1 puff PO once daily (COPD); 200/62.5/25 mcg QD (Asthma Step 5) IMPACT Trial (NEJM 2018; PMID 29668352 β†—) & CAPTAIN (Lancet RM 2020): Slashes exacerbations by 25% and all-cause mortality (NNT 105–147). βœ“ TRIAL CONCORDANT
Single-Inhaler Triple (MDI) Breztri Aerosphere
BGF MDI
160/9/4.8 mcg 2 puffs PO BID (Total daily: 320/18/9.6 mcg) ETHOS Trial (NEJM 2020; PMID 32579807 β†—): 24% exacerbation reduction and 46% mortality reduction (NNT 110–140). βœ“ TRIAL CONCORDANT
Dual LABA/LAMA Anoro Ellipta
UMEC/VI
62.5/25 mcg 1 puff PO once daily Superior to monotherapies and LABA/ICS in lung function and flare prevention. Core backbone for GOLD Groups B & E with BEC < 300. βœ“ TRIAL CONCORDANT
Inhaled Dual PDE3/4 Ohtuvayre
Ensifentrine Inhalation
3 mg / 3 mL unit-dose vial nebulized BID via standard jet nebulizer ENHANCE-1 & 2 Trials (AJRCCM 2023; PMID 37364283 β†—): Non-steroidal dual bronchodilator + anti-inflammatory; slashes flares by 36–42% (NNT 5–6). βœ“ TRIAL CONCORDANT
Biologic (Anti-IL4RΞ±) Dupixent
Dupilumab SC Pen
300 mg SC every 2 weeks (First FDA-approved biologic in COPD) BOREAS (NEJM 2023; PMID 37272521 β†—) & NOTUS (NEJM 2024; PMID 38767614 β†—): Slashes COPD exacerbations by 30–34% (NNT 2.7) in BEC β‰₯ 300 + CB. βœ“ TRIAL CONCORDANT
Biologic (Anti-IL5RΞ±) Fasenra
Benralizumab SC Pen
30 mg SC q4w x 3 doses, then every 8 weeks SIROCCO (Lancet 2016; PMID 27609408 β†—) & ZONDA (NEJM 2017; PMID 28530840 β†—): 51% flare reduction; 75% median oral steroid reduction (NNT 3.7). βœ“ TRIAL CONCORDANT
Biologic (Anti-TSLP) Tezspire
Tezepelumab SC Pen
210 mg SC every 4 weeks NAVIGATOR (NEJM 2021; PMID 33979488 β†—): 56% overall exacerbation reduction across all biomarker strata (Type 2-High and Type 2-Low). βœ“ TRIAL CONCORDANT
Oral PDE4 Inhibitor Daliresp
Roflumilast Tablet
500 mcg PO daily (Initiate at 250 mcg QD x 4 weeks to avoid GI discontinuation) REACT (Lancet 2015; PMID 25684586 β†—) & RE2SPOND (AJRCCM 2016; PMID 27585384 β†—): Reduces hospitalizations by 24% in chronic bronchitis with FEV1 < 50%. βœ“ TRIAL CONCORDANT
Macrolide Prophylaxis Azithromycin Tablet
Oral Antibiotic
250 mg PO daily OR 500 mg PO 3x/week (Monday, Wednesday, Friday) Albert et al. (NEJM 2011; PMID 21864166 β†—) & COLUMBUS (Lancet RM 2014; PMID 24746000 β†—): Both daily 250mg and TIW 500mg verified. Mandatory baseline ECG and sputum AFB. βœ“ TRIAL CONCORDANT
Smoking Cessation Chantix
Varenicline Tartrate
Days 1–3: 0.5 mg QD; Days 4–7: 0.5 mg BID; Day 8–12 wks: 1.0 mg PO BID with food/water EAGLES Trial (Lancet 2016; PMID 27116918 β†—): Continuous abstinence 21.8% vs 9.4% placebo (NNT 4–5). Neuropsychiatric safety proven in 8,144 patients. βœ“ TRIAL CONCORDANT
πŸ”¬ Landmark Clinical Trials & Number Needed to Treat (NNT) Library
Filter Trials by Disease Domain: 10 Categories β€’ Fully Verified PubMed Citations
🫁 COPD Landmark Phase 3 Clinical Trials & NNTGOLD 2025/2026 Evidence Standard
Trial & Citation Regimen / Molecules Patient Population Sample Exac NNT Secondary Endpoints & Mortality NNT Guideline Impact & Clinical Takeaway
IMPACT
NEJM 2018 [PMID 29668352 β†—]
FF/UMEC/VI 100/62.5/25 QD vs Dual LABA/LAMA vs LABA/ICS Symptomatic COPD with β‰₯1 moderate/severe exacerbation 10,355 3–4 (BEC β‰₯ 100) All-Cause Mortality NNT: 105–147 (HR 0.72 vs LABA/LAMA; P=0.011) Landmark trial establishing single-inhaler triple therapy superiority in reducing exacerbations and extending survival in exacerbators.
ETHOS
NEJM 2020 [PMID 32579807 β†—]
BGF 320/18/9.6 MDI BID vs Dual G/F vs B/F Moderate-to-very severe COPD with β‰₯1 exacerbation in prior year 8,509 3.2 All-Cause Mortality NNT: 110–140 (HR 0.54 for high-dose ICS vs G/F; P=0.01) Second landmark Phase 3 trial confirming all-cause mortality reduction and 24% exacerbation suppression with triple therapy.
BOREAS & NOTUS
NEJM 2023 / 2024
[BOREAS: 37272521 β†—] [NOTUS: 38767614 β†—]
Dupilumab 300 mg SC q2w vs Placebo on maximal Triple COPD with chronic bronchitis, FEV₁ < 70%, and BEC β‰₯ 300 cells/Β΅L 1,874 2.7 Pre-BD FEV₁ improvement: +160 mL vs +77 mL (P<0.001); SGRQ -3.4 pts First FDA-approved biologic in COPD (GOLD 2025): delivers 30–34% reduction in annualized exacerbations in Type 2 COPD.
ENHANCE-1 & 2
AJRCCM 2023 [PMID 37364283 β†—]
Ensifentrine 3 mg nebulized BID vs Placebo Moderate-to-severe symptomatic COPD on background bronchodilators 1,549 5–6 FEV₁ AUC0–12h increase +87 to +94 mL (P<0.001); E-RS dyspnea reduction First-in-class inhaled dual PDE3/PDE4 inhibitor approved in 2024; non-steroidal bronchodilator & anti-inflammatory without GI toxicity.
FLAME
NEJM 2016 [PMID 27181606 β†—]
Indacaterol/Glycopyrronium (LABA/LAMA) vs Salmeterol/Fluticasone (LABA/ICS) COPD with β‰₯1 exacerbation in prior year 3,362 16–18 (vs LABA/ICS) Dual LABA/LAMA reduced exacerbations by 11% (P=0.003); lower pneumonia (3.2% vs 4.8%) Established dual LABA/LAMA as preferred core backbone over LABA/ICS, avoiding steroid-induced bacterial pneumonia.
REDUCE
JAMA 2013 [PMID 23695200 β†—]
Prednisone 40 mg PO daily for 5 days vs 14 days Acute exacerbations presenting to emergency department 314 Non-inferior Hazard ratio for next exacerbation: 0.95 (90% CI 0.70–1.29); slashes steroid dose Defines global GOLD standard: Prednisone 40 mg PO daily for 5 days max. Prolonged steroid courses cause harm without benefit.
Albert et al. / COLUMBUS
NEJM 2011 / Lancet RM 2014
[Albert: 21864166 β†—] [COLUMBUS: 24746000 β†—]
Azithromycin 250 mg QD or 500 mg 3x/wk vs Placebo Exacerbation-prone COPD on maintenance therapy (former smokers) 1,234 3–4 Prolonged median time to first exacerbation (266 vs 174 days; HR 0.73, P<0.001) Recommended for former smokers on maximal triple therapy. Mandatory baseline ECG (QTc), audiogram, and sputum AFB culture.
REACT & RE2SPOND
Lancet 2015 / Lancet RM 2016
[REACT: 25684586 β†—] [RE2SPOND: 27585384 β†—]
Roflumilast 500 mcg PO daily vs Placebo Severe COPD (FEV₁ < 50%), chronic bronchitis, and prior hospitalization 3,273 5–7 13.2% exacerbation reduction; 24.3% reduction in hospitalizations Oral PDE4 inhibitor for chronic bronchitis phenotype with severe obstruction. Requires monitoring of GI tolerance and body weight.
PANTHEON & PEACE
Lancet RM 2014 / Lancet 2008
[PANTHEON: 24621680 β†—] [PEACE: 18555912 β†—]
N-acetylcysteine 600 mg PO BID or Carbocisteine 500 mg PO TID vs Placebo COPD with chronic bronchitis and recurrent exacerbations 2,013 6–7.4 High-dose NAC 600mg BID reduces flares by 22%; Carbocisteine reduces flares by 24.5% Guideline-endorsed mucolytics for sputum hypersecretion; thins tenacious mucus and prevents seasonal flare-ups.
🫁 COPD Landmark Phase 3 Clinical Trials & NNTGOLD 2025/2026 Evidence Standard
IMPACT (NEJM 2018) [PMID 29668352 β†—]
Triple Therapy
EXAC NNT3–4
SAMPLE10,355
MORTALITY NNT105–147
Regimen: FF/UMEC/VI 100/62.5/25 QD vs Dual LABA/LAMA vs LABA/ICS.
Landmark Impact: Landmark trial establishing single-inhaler triple therapy superiority in reducing exacerbations and extending survival in exacerbators.
ETHOS (NEJM 2020) [PMID 32579807 β†—]
Triple MDI
EXAC NNT3.2
SAMPLE8,509
MORTALITY NNT110–140
Regimen: BGF 320/18/9.6 MDI BID vs Dual G/F vs B/F.
Landmark Impact: Second landmark Phase 3 trial confirming all-cause mortality reduction and 24% exacerbation suppression with triple therapy.
BOREAS & NOTUS (NEJM 2023/24) [PMID 37272521 β†—]
Anti-IL-4RΞ± Biologic
EXAC NNT2.7
SAMPLE1,874
FEV₁ GAIN+160 mL
Regimen: Dupilumab 300 mg SC q2w vs Placebo on maximal Triple.
Landmark Impact: First FDA-approved biologic in COPD (GOLD 2025): delivers 30–34% reduction in annualized exacerbations in Type 2 COPD.
ENHANCE-1 & 2 (AJRCCM 2023) [PMID 37364283 β†—]
PDE3/4 Inhaled
EXAC NNT5–6
SAMPLE1,549
FEV₁ GAIN+94 mL
Regimen: Ensifentrine 3 mg nebulized BID vs Placebo.
Landmark Impact: First-in-class inhaled dual PDE3/PDE4 inhibitor approved in 2024; non-steroidal bronchodilator & anti-inflammatory without GI toxicity.
FLAME (NEJM 2016) [PMID 27181606 β†—]
Dual Bronchodilator
EXAC NNT16–18
SAMPLE3,362
PRIMARY EFFECT16–18 (vs LABA/ICS)
Regimen: Indacaterol/Glycopyrronium (LABA/LAMA) vs Salmeterol/Fluticasone (LABA/ICS).
Landmark Impact: Established dual LABA/LAMA as preferred core backbone over LABA/ICS, avoiding steroid-induced bacterial pneumonia.
REDUCE (JAMA 2013) [PMID 23695200 β†—]
Steroid Stewardship
EXAC NNTNon-inferior
SAMPLE314
PRIMARY EFFECTNon-inferior
Regimen: Prednisone 40 mg PO daily for 5 days vs 14 days.
Landmark Impact: Defines global GOLD standard: Prednisone 40 mg PO daily for 5 days max. Prolonged steroid courses cause harm without benefit.
Albert et al. / COLUMBUS (NEJM 2011 / Lancet 2016) [PMID 21864166 β†—]
Macrolide Prophylaxis
EXAC NNT3–4
SAMPLE1,234
PRIMARY EFFECT3–4
Regimen: Azithromycin 250 mg QD or 500 mg 3x/wk vs Placebo.
Landmark Impact: Recommended for former smokers on maximal triple therapy. Mandatory baseline ECG (QTc), audiogram, and sputum AFB culture.
REACT & RE2SPOND (Lancet 2015) [PMID 25684586 β†—]
Oral PDE4
EXAC NNT5–7
SAMPLE3,273
PRIMARY EFFECT5–7
Regimen: Roflumilast 500 mcg PO daily vs Placebo.
Landmark Impact: Oral PDE4 inhibitor for chronic bronchitis phenotype with severe obstruction. Requires monitoring of GI tolerance and body weight.
PANTHEON & PEACE (Lancet RM 2014 / Lancet 2008) [PMID 24621680 β†—]
Mucolytics / Antioxidant
EXAC NNT6–7.4
SAMPLE2,013
PRIMARY EFFECT6–7.4
Regimen: N-acetylcysteine 600 mg PO BID or Carbocisteine 500 mg PO TID vs Placebo.
Landmark Impact: Guideline-endorsed mucolytics for sputum hypersecretion; thins tenacious mucus and prevents seasonal flare-ups.
Home Nocturnal NIV (Owens / Lincare)
Persistent PaCOβ‚‚ > 53 post-flare
AVAPS NIV
πŸ›Œ Epworth Sleepiness Scale (ESS)
Score: 0/24
Rate chance of dozing (0 = would never, 1 = slight, 2 = moderate, 3 = high):
πŸ“Š Sleep Study Order Generator
Diagnostic Plan
⚑ Non-Invasive Mechanical Ventilation (NIV / AVAPS)
DME Qualification
πŸ“‹ Exact Word-for-Word DME Qualification Text:
Arozullah Class II (1.8% Failure) β€’ Canet Intermediate (13.3%)
Intraoperative 6 mL/kg Lung Protection
INTERMEDIATE
1 Planned Surgical Procedure
2 Patient Risk Factors
πŸ“ Pre-Op Pulmonary Consultation Output
Solid Nodule 6–8 mm β€’ High Risk
Fleischner 2024 Protocol: CT Chest at 6–12 months, then CT at 18–24 months
CT 6-12M
1 Nodule Morphology & Multiplicity
2 Size & Patient Risk
πŸ“‹ Fleischner Society 2024 Management Recommendation