Asthma–COPD Overlap (ACO) — GINA/GOLD 2026 ICS-foundation
Encounter flow
12/12 authoredCanonical 12-phase frame with authored status for this dossier.
Frame
Confirm PERSISTENT airflow limitation (post-BD FEV1/FVC <0.70) PLUS features of BOTH asthma and COPD — ACO is a clinical description, not a single disease (GINA 2026 / GOLD 2026 joint ACO chapter)
Fixed obstruction confirmed AND mixed asthma+COPD features documented
Patient inputs (15)
Age of asthma onset (<40 supports asthma component) + biologic eligibility; GINA/GOLD 2026 syndromic criteria
Prior physician diagnosis of asthma (esp. <40 yr) is the single most reliable ACO criterion (Barrecheguren PMID 25405671; Caillaud PMID 27501862)
Personal/family atopy, allergic rhinitis, IgE sensitisation — minor ACO criterion (Cataldo PMID 28243078; OR hay-fever 5.50 PMID 27501862)
Noxious-exposure burden (≥10 pack-years) establishes the COPD component; smoking blunts ICS response (GOLD 2026; Cataldo PMID 28243078)
Variable symptoms (diurnal/nocturnal, episodic) favour an asthma component vs the slowly-progressive COPD pattern (GINA 2026 Box 1-2)
ACO carries a higher exacerbation burden than COPD alone (IRR 1.65, Jo/Rhee PMID 31953230); drives escalation
Symptom burden tracking (mMRC/CAT) — drives review cadence and escalation (GOLD 2026 Assessment; CHAIN PMID 27684372)
Detect SABA-only or LABA-LAMA-WITHOUT-ICS — both AVOIDED when an asthma component is present (the key ACO safety teaching point; GINA/GOLD 2026)
Acute exacerbation severity + LTOT eligibility in the COPD component (GOLD 2026)
Post-BD FEV1/FVC <0.70 (fixed, COPD) WITH bronchodilator reversibility ≥12% AND ≥200 mL (asthma) — the defining objective ACO dyad (Cataldo PMID 28243078; GINA/GOLD 2026)
Eosinophilic-COPD treatable trait: ≥300 cells/µL predicts ICS-response in ACO (Jo/Rhee IRR 0.52 PMID 31953230) + biologic eligibility (BOREAS PMID 37272521); the eosinophil pivot is FOR ICS here, not against it
DLCO preserved/normal favours asthma component; markedly reduced + restriction favours ILD mimic (differential discriminator)
FeNO marks T2 inflammation; supports asthma component + predicts ICS/dupilumab response (GINA 2026 Box 3-4; Cataldo minor criterion PMID 28243078)
IgE sensitisation supports the atopic asthma component; omalizumab eligibility in severe-T2 ACO (Sposato PMID 30043557)
Exclude bronchiectasis/ILD/cancer mimics; HRCT signet-ring vs UIP vs emphysema discriminates (research bundle §3)
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Severity triggers (5)
- informationalsevereaco_severe_exacerbationAcute severe ACO exacerbation — behaves like the WORSE of asthma and COPD (higher exacerbation burden than COPD alone, IRR 1.65, Jo/Rhee PMID 31953230): severe airflow obstruction + hypoxia, OR life-threatening asthma-like features (silent chest, exhaustion), OR type-II respiratory failure (COPD component)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderateaco_frequent_exacerbator≥2 moderate exacerbations OR ≥1 hospitalisation in 12 months despite triple ICS/LABA/LAMA with verified technique — refractory ACO (GINA 2026 Step 5; ATS/ERS 2024)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderateics_containing_foundation_mandatoryACO confirmed (fixed post-BD FEV1/FVC <0.70 + asthma component) — an ICS-CONTAINING regimen is the FLOOR. SABA-only and LABA-LAMA-WITHOUT-ICS are CONTRAINDICATED while an asthma component is present (the defining ACO teaching point — the INVERSE of eos-gated COPD)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderateeosinophil_feno_ics_biologic_decisionBlood eosinophils + FeNO drive the ICS/biologic decision chain — but in the INVERSE direction to COPD: eos ≥300 (or sputum eos ≥2.5%) → STRONG ICS-responder (reinforces the ICS floor) AND biologic-eligible if refractory; sputum eos ≥2.5% test characteristic 82.4% sens / 84.8% spec for ICS-responsive overlap (Kitaguchi PMID 22589579; Jo/Rhee PMID 31953230)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderatediscriminate_asthma_vs_copd_vs_aco§5.5.2 discrimination-as-data — the CORE of this engine. Is it pure ASTHMA, pure COPD, or ACO? Syndromic-feature score with test characteristics: post-BD FEV1/FVC <0.70 fixed (present in COPD AND ACO; ABSENT in pure asthma) + bronchodilator reversibility ≥12% AND ≥200 mL or FEV1 variability ≥400 mL (present in asthma AND ACO; minimal in pure COPD) + asthma diagnosis <40 yr (strong asthma/ACO criterion) + atopy/IgE + eos/FeNO↑ + ≥10 pk-yr smoking (COPD/ACO). ACO = fixed obstruction AND large reversibility/variability AND asthma-history/eosinophilia/atopy (Cataldo Belgian consensus PMID 28243078; Barrecheguren PMID 25405671)Trigger could not be auto-evaluated — needs clinician judgement.
Workflow calculators
Run this disease's risk and dosing calculators inline.
Recommended regimen
ACO ICS-containing foundation — ICS/LABA → triple ICS/LABA/LAMA (GINA/GOLD 2026 joint)- budesonide-formoterolfirst lineICS_LABA160/4.5 µg 2 puffs BID (or per asthma-component severity) • inhaled • BID (MART possible for the asthma component)triggers: aco_confirmed, asthma_component_presentICS-containing foundation per GINA/GOLD 2026 joint ACO description — ICS treats the eosinophilic/asthma component; budesonide-formoterol also supports a MART reliever strategy. RxCUI 19831 = budesonide IN (combination — NEEDS_RXNAV_VALIDATION for SCD/SBD; not hand-authored)rxcui 1246304
- fluticasone furoate-vilanterolfirst lineICS_LABA100/25 µg or 200/25 µg Ellipta 1 inhalation daily • inhaled • once dailytriggers: aco_confirmed, once_daily_preferenceAlternative once-daily ICS/LABA foundation (GINA/GOLD 2026). RxCUI 41126 = combination base-ingredient code — NEEDS_RXNAV_VALIDATION for SCD/SBDrxcui 1424889
outpatient playbook — drug actions (4)
- 1. ICS/LABA foundationBudesonide-formoterol 160/4.5 µg 2 puffs BID OR fluticasone furoate-vilanterol 100-200/25 µg daily • inhaled • BID / once dailytrigger: ACO confirmed (asthma component present)ICS-containing FLOOR per GINA/GOLD 2026 — never SABA-only/LABA-LAMA-without-ICS
- 2. Triple ICS/LABA/LAMAFluticasone furoate-umeclidinium-vilanterol 100-200/62.5/25 µg Ellipta daily OR budesonide-glycopyrrolate-formoterol 160/9/4.8 µg MDI 2 puffs BID • inhaled • once daily / BIDtrigger: Persistent symptoms or ≥1 exacerbation on ICS/LABAAdd LAMA — ICS retained as the foundation (GINA/GOLD 2026)
- 3. Severe-T2 biologicDupilumab 200-300 mg SC q2w; omalizumab per IgE/weight q2-4w; mepolizumab 100 mg SC q4w; tezepelumab 210 mg SC q4w • SC • q2-4 weekstrigger: Persistent exacerbations on triple + T2 trait (eos/FeNO/IgE)QUEST/BOREAS/Sposato/NAVIGATOR — phenotype-gated biologic
- 4. Smoking-cessation pharmacotherapyVarenicline 0.5 mg → 1 mg BID; bupropion SR 150 mg BID; NRT patch + lozenge • PO/transdermal • per agenttrigger: Active smokerHighest-impact intervention — smoking blunts ICS response (GOLD 2026 Follow-up & Prevention)
Auto-drafted A&P note
outpatientSubjective
- Possible entry pathways: Persistent airflow limitation WITH features of both asthma and COPD (variable + persistent obstruction, smoking + atopy) — GINA 2026 / GOLD 2026 joint ACO description; Post-BD FEV1/FVC <0.70 (fixed, COPD-like) AND large bronchodilator reversibility (≥12% AND ≥200 mL, or FEV1 variability ≥400 mL — asthma-like) (Cataldo PMID 28243078); Established COPD with a documented physician diagnosis of asthma before age 40 (Caillaud/Roche INITIATIVES BPCO PMID 27501862).
Objective
- No vitals, labs, or imaging entered for this encounter.
Assessment
**Asthma–COPD Overlap (ACO) — GINA/GOLD 2026 ICS-foundation** (pulm.aco.v1). Phenotype framing: §5.5.2 discrimination-as-data — the CORE of this engine: ASTHMA (early onset, fully reversible, non-smoker, no fixed obstruction) vs COPD (≥10 pk-yr, fixed obstruction, eos-gated ICS, minimal reversibility) vs ACO (BOTH — fixed post-BD FEV1/FVC <0.70 AND large BDR/variability AND eosinophilia/atopy/asthma-history). Syndromic-feature score: major = high BDR (>200 mL & ≥12%) + asthma dx <40; minor = atopy/IgE, eos/FeNO↑, symptom variability (Cataldo PMID 28243078). Sputum eos ≥2.5% predicts ICS response (82.4% sens / 84.8% spec, Kitaguchi PMID 22589579) Scope: Confirm PERSISTENT airflow limitation (post-BD FEV1/FVC <0.70) PLUS features of BOTH asthma and COPD — ACO is a clinical description, not a single disease (GINA 2026 / GOLD 2026 joint ACO chapter) No severity triggers fired against current inputs.
Plan
Regimen axis: **ACO ICS-containing foundation — ICS/LABA → triple ICS/LABA/LAMA (GINA/GOLD 2026 joint)** — step "Tier 1 — ICS/LABA foundation (NEVER SABA-only, NEVER LABA-LAMA-without-ICS)". 1. budesonide-formoterol 160/4.5 µg 2 puffs BID (or per asthma-component severity) inhaled BID (MART possible for the asthma component) (ICS_LABA, first line) — ICS-containing foundation per GINA/GOLD 2026 joint ACO description — ICS treats the eosinophilic/asthma component; budesonide-formoterol also supports a MART reliever strategy. RxCUI 19831 = budesonide IN (combination — NEEDS_RXNAV_VALIDATION for SCD/SBD; not hand-authored) 2. fluticasone furoate-vilanterol 100/25 µg or 200/25 µg Ellipta 1 inhalation daily inhaled once daily (ICS_LABA, first line) — Alternative once-daily ICS/LABA foundation (GINA/GOLD 2026). RxCUI 41126 = combination base-ingredient code — NEEDS_RXNAV_VALIDATION for SCD/SBD Setting playbook (outpatient) — Confirm ACO (discriminate from pure asthma / pure COPD), establish and maintain an ICS-CONTAINING regimen as the foundation, reduce the (higher-than-COPD) exacerbation burden, and refer severe-T2 refractory disease for biologic assessment (GINA/GOLD 2026) 3. ICS/LABA foundation Budesonide-formoterol 160/4.5 µg 2 puffs BID OR fluticasone furoate-vilanterol 100-200/25 µg daily inhaled BID / once daily — ACO confirmed (asthma component present) (ICS-containing FLOOR per GINA/GOLD 2026 — never SABA-only/LABA-LAMA-without-ICS) 4. Triple ICS/LABA/LAMA Fluticasone furoate-umeclidinium-vilanterol 100-200/62.5/25 µg Ellipta daily OR budesonide-glycopyrrolate-formoterol 160/9/4.8 µg MDI 2 puffs BID inhaled once daily / BID — Persistent symptoms or ≥1 exacerbation on ICS/LABA (Add LAMA — ICS retained as the foundation (GINA/GOLD 2026)) 5. Severe-T2 biologic Dupilumab 200-300 mg SC q2w; omalizumab per IgE/weight q2-4w; mepolizumab 100 mg SC q4w; tezepelumab 210 mg SC q4w SC q2-4 weeks — Persistent exacerbations on triple + T2 trait (eos/FeNO/IgE) (QUEST/BOREAS/Sposato/NAVIGATOR — phenotype-gated biologic) 6. Smoking-cessation pharmacotherapy Varenicline 0.5 mg → 1 mg BID; bupropion SR 150 mg BID; NRT patch + lozenge PO/transdermal per agent — Active smoker (Highest-impact intervention — smoking blunts ICS response (GOLD 2026 Follow-up & Prevention)) Non-pharmacologic actions: - Pulmonary rehabilitation referral — especially after any exacerbation; within 3 weeks - Allergen / trigger avoidance counselling (asthma component) - Annual influenza, PCV20 (or PCV15+PPSV23), RSV (≥60), COVID, Tdap - Lung cancer screening — annual LDCT if 50-80 yr, ≥20 pack-years, current or quit ≤15 yr (USPSTF 2021) - Written ACO action plan (green/yellow/red) incorporating both components - Weight management / OSA + GERD optimisation (obesity over-represented in ACO — PMID 27501862) AVOID / contraindication checks: - ACO_never_SABA_only_maintenance_ICS_containing_regimen_mandatory (GINA 2026 §5 ACO; GOLD 2026 joint description) - ACO_avoid_LABA_LAMA_without_ICS_when_asthma_component_present (GINA/GOLD 2026 — the defining ACO contraindication; inverse of COPD eos gated ICS) - ACO_do_not_apply_COPD_ICS_withdrawal_WISDOM_logic_while_asthma_component_persists (WISDOM PMID 25196117 logic is COPD only — does NOT transfer to the asthma component of ACO) - ICS_pneumonia_risk_acknowledged_but_outweighed_by_asthma_component_benefit_in_ACO (FLAME pneumonia 4.8% vs 3.2% P=0.02 PMID 27181606 — risk noted; ICS still foundational in ACO unlike eos low pure COPD) - Beta_blocker_avoid_nonselective_cardioselective_OK_if_strong_CV_indication (GINA 2026 §3; GOLD 2026 Multimorbidity) - Pregnancy_continue_ICS_containing_regimen_uncontrolled_disease_worse_than_drug_avoid_roflumilast (GINA 2026 §3 pregnancy; GOLD 2026) - Smoking_cessation_highest_impact_intervention_smoking_blunts_ICS_response (GOLD 2026 Follow up & Prevention; Cataldo PMID 28243078) - Biologic_eligibility_gate_by_T2_phenotype_eos_FeNO_IgE_before_initiation (ATS/ERS 2024; GINA 2026 Step 5; Sposato PMID 30043557)
Monitoring
Regimen monitoring: - annual spirometry track fixed obstruction and reversibility (GINA/GOLD 2026) - blood eos and FeNO to track T2 trait and biologic candidacy (eos >=300 = strong ICS-responder, Jo/Rhee IRR 0.52 PMID 31953230) - mMRC or CAT q visit symptom burden (GOLD 2026 Assessment; CHAIN PMID 27684372) - ACT q visit for the asthma component (<20 = uncontrolled step-up trigger; GINA 2026 Box 2-2) - exacerbation diary ACO burden exceeds COPD alone (IRR 1.65, Jo/Rhee PMID 31953230) - inhaler technique and adherence q visit BEFORE any step up (GINA 2026 §3) - biologic response at 4 months >=50pct exac reduction = responder (ATS/ERS 2024) - lung function decline may be slower than pure COPD when treated (-13.9 vs -29.3 mL/yr, Park/Sin KOLD PMID 29499758 — appropriate ICS-containing therapy matters) - NEVER withdraw ICS while asthma component persists (inverse of COPD ICS-deprescribing — GINA/GOLD 2026) Setting (outpatient) monitoring: - Spirometry annually (track fixed obstruction + reversibility) - Blood eos + FeNO to track the T2 trait and biologic candidacy - mMRC + CAT + ACT each visit - Inhaler technique + adherence each visit BEFORE step-up - Exacerbation diary (burden exceeds COPD alone) Follow-up plan: Written action plan, vaccinations (influenza, pneumococcal PCV20 or PCV15+PPSV23, RSV, COVID, Tdap), smoking-cessation reinforcement, pulmonary rehab within 3 weeks of any exacerbation, allergen/trigger control, 1-week post-exacerbation follow-up, advance-care planning in advanced disease (GINA/GOLD 2026) - Close-out criterion: Prevention bundle + rehab referral + follow-up complete Monitoring phase: Annual spirometry, exacerbation diary, inhaler technique audit (BEFORE any step-up), mMRC/CAT each visit, blood eos + FeNO to track the T2 trait and biologic candidacy, biologic response at 4 months; never withdraw ICS while the asthma component persists (the inverse of COPD ICS-deprescribing) (GINA/GOLD 2026; ATS/ERS 2024)
Disposition
Current setting: outpatient — Confirm ACO (discriminate from pure asthma / pure COPD), establish and maintain an ICS-CONTAINING regimen as the foundation, reduce the (higher-than-COPD) exacerbation burden, and refer severe-T2 refractory disease for biologic assessment (GINA/GOLD 2026) Disposition criteria: - Continue ICS-containing regimen if controlled; step up if exacerbation pattern worsens - Reclassify to pulm.asthma.core.v1 or pulm.copd.core.v1 if discrimination shows a single dominant disease (do NOT keep on the ACO pathway if criteria are not met) - Refer for biologic assessment if severe-T2 refractory on triple Escalation triggers (move to higher acuity): - Acute severe exacerbation with O2 requirement / life-threatening features → ED (treat as worse-of-both physiology) - Persistent uncontrolled on triple with ≥2 exacerbations/yr → severe-asthma/ACO specialty clinic for biologic assessment (ATS/ERS 2024) - Diagnostic uncertainty (is it pure asthma, pure COPD, bronchiectasis, IPF?) → re-route via the discrimination workup
Earlier-Return Triggers
Return-precaution thresholds (watch for): - [SEVERE] Acute severe ACO exacerbation — behaves like the WORSE of asthma and COPD (higher exacerbation burden than COPD alone, IRR 1.65, Jo/Rhee PMID 31953230): severe airflow obstruction + hypoxia, OR life-threatening asthma-like features (silent chest, exhaustion), OR type-II respiratory failure (COPD component) - [MODERATE] ≥2 moderate exacerbations OR ≥1 hospitalisation in 12 months despite triple ICS/LABA/LAMA with verified technique — refractory ACO (GINA 2026 Step 5; ATS/ERS 2024) - [MODERATE] ACO confirmed (fixed post-BD FEV1/FVC <0.70 + asthma component) — an ICS-CONTAINING regimen is the FLOOR. SABA-only and LABA-LAMA-WITHOUT-ICS are CONTRAINDICATED while an asthma component is present (the defining ACO teaching point — the INVERSE of eos-gated COPD)
Citations
- GINA 2026 Strategy Report (released May 2026) + GOLD 2026 Report — JOINT asthma–COPD overlap (ACO) description (ACO is a clinical description, not a single disease; ICS-containing therapy foundational) [PMID:33209021](https://pubmed.ncbi.nlm.nih.gov/33209021/) - Cited evidence (PMID 27501862) [PMID:27501862](https://pubmed.ncbi.nlm.nih.gov/27501862/) - Cited evidence (PMID 27684372) [PMID:27684372](https://pubmed.ncbi.nlm.nih.gov/27684372/) - Cited evidence (PMID 31953230) [PMID:31953230](https://pubmed.ncbi.nlm.nih.gov/31953230/) - Cited evidence (PMID 22589579) [PMID:22589579](https://pubmed.ncbi.nlm.nih.gov/22589579/) Last reconciled with current guidelines: 2026-05-25.
- GINA 2026 Strategy Report (released May 2026) + GOLD 2026 Report — JOINT asthma–COPD overlap (ACO) description (ACO is a clinical description, not a single disease; ICS-containing therapy foundational) — PMID:33209021
- Cited evidence (PMID 27501862) — PMID:27501862
- Cited evidence (PMID 27684372) — PMID:27684372
- Cited evidence (PMID 31953230) — PMID:31953230
- Cited evidence (PMID 22589579) — PMID:22589579