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COPD Management: 8 Essential Steps for GOLD-Based Therapy

Clinical Practice Update — GOLD-Based Inhaler Selection, Exacerbation Prevention, and the Role of Eosinophils

This is an original clinical education article informed by current guidelines and evidence. See References below for source documents.

MDA-COPD-2026·14 min read
Clinical Focus
Translating recent COPD updates into a usable clinic workflow for adults with stable disease
Target Audience
Primary care physicians, internal medicine, residents, respiratory nurses, clinical pharmacists
Setting
Primary care, general internal medicine outpatient, post-hospital follow-up
Source Evidence
  • GOLD 2024 Report — Global Strategy for COPD Diagnosis, Management and Prevention
  • NICE Guideline NG115 — COPD in over 16s: diagnosis and management (2019, updated 2024)
  • ETHOS Trial — Triple Inhaled Therapy at Two Doses in COPD (NEJM, 2020)
  • IMPACT Trial — Once-Daily Single-Inhaler Triple vs Dual Therapy (NEJM, 2018)
  • LOTT Trial — Long-Term Oxygen Treatment Trial (NEJM, 2016)

Key Clinical Takeaways

Modern COPD management hinges on three repeatable clinic decisions: assess symptoms and exacerbation risk, choose and escalate inhalers in a structured way, and layer in the non-pharmacological pillars (vaccination, pulmonary rehabilitation, oxygen). The takeaways below condense the practical core of effective COPD management into moves you can make at every visit.

Clinical workflow for COPD management showing GOLD-based inhaler selection eosinophil-guided therapy and exacerbation prevention
Practical clinic workflow for COPD management: assess, classify, prescribe, prevent, refer.
  • 1Confirm COPD with post-bronchodilator spirometry (FEV1/FVC < 0.70) before any long-term inhaler is started.
  • 2Classify every patient with GOLD ABE: A = low symptoms / low risk, B = high symptoms / low risk, E = any high-risk exacerbator.
  • 3Start LABA + LAMA dual therapy as the default in Group B and Group E, not LABA monotherapy.
  • 4Add inhaled corticosteroid (triple therapy) when blood eosinophils ≥ 300 cells/µL or exacerbations continue on LABA + LAMA.
  • 5Avoid ICS-containing regimens when eosinophils are below 100 cells/µL — pneumonia risk outweighs benefit.
  • 6Offer annual influenza, age-appropriate pneumococcal vaccination, updated COVID-19 dose, RSV (≥ 60), and a one-off Tdap.
  • 7Refer every symptomatic patient (mMRC ≥ 2) and every patient discharged from an exacerbation to pulmonary rehabilitation within 4 weeks.
  • 8Prescribe long-term oxygen only for severe resting hypoxaemia (PaO&sub2; ≤ 55 mmHg or SpO&sub2; ≤ 88%); moderate desaturation alone is not an indication.
  • 9Reassess inhaler technique, adherence, and ongoing tobacco use at every visit before escalating therapy.
  • 10Smoking cessation and pulmonary rehabilitation remain the only interventions, alongside oxygen in selected patients, that change mortality.

Assessing Symptoms and Exacerbation Risk in COPD Management

Effective COPD management starts with a structured assessment at every visit. Two questions drive the rest of the plan: How symptomatic is the patient today, and how many exacerbations have they had in the last year? The answers map cleanly to the GOLD ABE groups, which replaced the older ABCD framework in 2023 and remain the basis for inhaler choice in 2024.

Before any pharmacological change, always check the foundation: confirmed spirometry, ongoing smoking cessation support if the patient still smokes, inhaler technique, and adherence. Escalating therapy on top of poor technique only increases cost and side effects.

1

Confirm a post-bronchodilator FEV1/FVC ratio below 0.70 on spirometry before labelling any patient with COPD or starting maintenance inhalers.

Strong Rec High Evidence GOLD 2024 NICE NG115
2

Quantify symptoms at every visit using either the CAT score (8 items, score 0–40) or the mMRC dyspnoea scale (0–4). Cut-offs of CAT ≥ 10 or mMRC ≥ 2 indicate “high symptoms” for ABE classification.

Strong Rec Moderate Evidence GOLD 2024
3

Document exacerbation history over the last 12 months. Two or more moderate exacerbations, or any single exacerbation requiring hospital admission, places the patient in Group E regardless of symptom score.

Strong Rec High Evidence GOLD 2024
4

Check a blood eosinophil count at diagnosis and before any escalation that involves inhaled corticosteroid. The result is one of the strongest predictors of ICS response in COPD management.

Moderate Rec Moderate Evidence GOLD 2024
5

Screen for the major comorbidities that change prognosis and treatment: cardiovascular disease, anxiety and depression, osteoporosis, sleep-disordered breathing, and lung cancer in eligible smokers.

Moderate Rec Low Evidence GOLD 2024
Clinical Pearl: A patient with mMRC = 1 and one mild exacerbation can still be Group A — but ask about “cold chest infections that needed antibiotics or steroids”. Many patients underreport exacerbations because they were managed at home.

Initial Inhaler Selection in COPD Management

First-line inhaler choice in COPD management is driven by the GOLD ABE group, not by FEV1 percent predicted. The 2024 update keeps three simple starting points: monotherapy for the least symptomatic, dual bronchodilation for most, and selective use of inhaled corticosteroid for patients with a strong exacerbation or eosinophil phenotype.

6

For Group A (low symptoms, low risk), start a single long-acting bronchodilator — either a LAMA (e.g., tiotropium 18 µg daily) or LABA. LAMA is preferred for its slightly stronger exacerbation reduction.

Strong Rec High Evidence GOLD 2024
7

For Group B (high symptoms, low risk), start LABA + LAMA in a single combination inhaler. Dual bronchodilation outperforms either component alone on dyspnoea, lung function, and quality of life.

Strong Rec High Evidence GOLD 2024
8

For Group E (any high-risk exacerbator), start LABA + LAMA. Add an ICS up front (i.e., triple therapy) when blood eosinophils ≥ 300 cells/µL or there is a coexisting asthma phenotype.

Strong Rec High Evidence GOLD 2024
9

Do not start LABA + ICS (without LAMA) as first-line COPD therapy. The combination has been superseded by LABA + LAMA and by triple therapy where ICS is indicated.

Against Moderate Evidence GOLD 2024
10

Match the inhaler device to the patient. Soft-mist or dry-powder devices need different inspiratory flow rates from metered-dose inhalers; a poor match wastes the prescription.

Strong Rec Moderate Evidence NICE NG115

GOLD ABE Groups at a Glance

Group A: 0–1 moderate exacerbation/year, CAT < 10 or mMRC 0–1. Group B: 0–1 moderate exacerbation/year, CAT ≥ 10 or mMRC ≥ 2. Group E: ≥ 2 moderate exacerbations/year OR any exacerbation requiring hospitalisation (symptom level does not change the group).

Stepwise Inhaler Escalation in COPD Management

Escalation in COPD management is a follow-up decision, not the first decision. Two follow-up tracks matter: persistent dyspnoea despite treatment, and persistent exacerbations despite treatment. The route up the ladder is different for each.

11

For persistent dyspnoea on a single bronchodilator, escalate to LABA + LAMA before adding ICS. Most breathlessness responds to dual bronchodilation alone.

Strong Rec High Evidence GOLD 2024
12

For continued exacerbations on LABA + LAMA, escalate to single-inhaler triple therapy (LABA + LAMA + ICS) when eosinophils ≥ 100 cells/µL, and especially when ≥ 300 cells/µL.

Strong Rec High Evidence ETHOS 2020 IMPACT 2018
13

Prefer a single-inhaler triple over three separate inhalers when available. Single-device regimens improve adherence and may reduce all-cause mortality compared with dual therapy in patients with frequent exacerbations.

Moderate Rec Moderate Evidence ETHOS 2020
14

Consider stepping down ICS in patients on triple therapy who have had no exacerbations for 12 months and whose eosinophils are below 300 cells/µL. Watch for symptom rebound over the next 3 months.

Conditional Rec Moderate Evidence GOLD 2024
15

Before escalating any patient, recheck three things: confirmed COPD diagnosis on spirometry, inhaler technique observed in clinic, and adherence over the prior 3 months. Most “treatment failure” is one of those.

Strong Rec Low Evidence NICE NG115
Warning
Inhaled corticosteroid in COPD increases pneumonia risk, particularly in older patients, those with low BMI, and those with severe airflow limitation. Use ICS only where the exacerbation or eosinophil signal justifies it.
Clinical Pearl: If a patient on triple therapy still exacerbates, the next step is rarely a different inhaler — it is pulmonary rehabilitation, vaccination review, and consideration of roflumilast or azithromycin.

Eosinophil-Guided Therapy: Who Benefits From ICS

The most clinically useful biomarker in routine COPD management is the blood eosinophil count from a standard CBC. Higher counts predict a larger exacerbation reduction from inhaled corticosteroid and a smaller increase in pneumonia risk relative to that benefit. Lower counts predict the opposite.

Use blood eosinophils as a continuous variable rather than a binary switch. The relationship between eosinophil count and ICS response is gradient: more eosinophils, more benefit. Confirm the result on a stable visit (not during an exacerbation) and ideally on more than one occasion.

16

Initiate or continue ICS-containing therapy when blood eosinophils ≥ 300 cells/µL in any patient with a history of exacerbations.

Strong Rec High Evidence GOLD 2024
17

Consider ICS-containing therapy when eosinophils are 100–299 cells/µL in patients who continue to exacerbate on LABA + LAMA.

Conditional Rec Moderate Evidence GOLD 2024
18

Avoid ICS in patients with eosinophils persistently below 100 cells/µL. The number needed to harm for pneumonia approaches or exceeds the number needed to treat for exacerbation prevention.

Against Moderate Evidence GOLD 2024

Exacerbation Prevention: Beyond Inhalers

Two add-on oral therapies remain useful in selected patients who continue to exacerbate despite optimal triple therapy. Each has a narrow indication and meaningful side effects, so they belong to a specific COPD management phenotype rather than to everyone.

19

Consider roflumilast 500 µg once daily in patients with FEV1 < 50% predicted, chronic bronchitis phenotype, and frequent exacerbations on triple therapy. Start at 250 µg daily for the first 4 weeks to reduce nausea and weight loss.

Conditional Rec Moderate Evidence GOLD 2024
20

Consider chronic azithromycin (250 mg daily or 500 mg three times weekly) in former smokers with persistent exacerbations on optimised inhaler therapy. Screen for baseline QT prolongation, hearing loss, and atypical mycobacteria before starting.

Conditional Rec Moderate Evidence GOLD 2024
21

Provide every patient with a written self-management action plan that identifies their personal early-warning signs and includes a short course of prednisolone and an appropriate antibiotic for use if those signs occur.

Moderate Rec Moderate Evidence NICE NG115
22

Offer tobacco cessation support at every visit to every patient who still smokes — brief counselling, varenicline, nicotine replacement, or bupropion. Quitting remains the single most important intervention to slow lung function decline.

Strong Rec High Evidence GOLD 2024 NICE NG115

Vaccination in COPD: A Short Annual Checklist

Vaccination is one of the cheapest, highest-impact interventions in routine COPD management. Most exacerbations are triggered by respiratory infection, so prevention pays off. The current panel is broader than influenza alone.

23

Administer the seasonal influenza vaccine every year. Influenza vaccination reduces exacerbations and hospital admissions in people with COPD.

Strong Rec High Evidence GOLD 2024
24

Offer age-appropriate pneumococcal vaccination — in most regions, PCV20 alone, or PCV15 followed by PPSV23 at least one year later, for adults with COPD.

Strong Rec Moderate Evidence GOLD 2024
25

Ensure the patient has an up-to-date COVID-19 vaccine appropriate for the current season and local public health schedule.

Strong Rec Moderate Evidence GOLD 2024
26

Offer a single dose of RSV vaccine to adults aged 60 and older with COPD, in line with current local immunisation recommendations.

Moderate Rec Moderate Evidence GOLD 2024
27

Ensure a one-off adult Tdap is on record for every patient with COPD who has not previously received it. Pertussis can precipitate severe exacerbations.

Moderate Rec Low Evidence GOLD 2024

Pulmonary Rehabilitation: The Most Under-Used Intervention

Pulmonary rehabilitation is one of the few interventions in COPD that improves exercise capacity, dyspnoea, and quality of life across all severity levels, and it reduces 12-month readmission after an exacerbation. It is also one of the most consistently under-referred treatments in routine practice.

28

Refer every patient with symptomatic COPD (mMRC ≥ 2 or CAT ≥ 10) to a structured pulmonary rehabilitation programme of at least 6–8 weeks, with supervised exercise plus disease education.

Strong Rec High Evidence GOLD 2024 NICE NG115
29

Initiate pulmonary rehabilitation within 4 weeks of discharge for any patient hospitalised with an exacerbation. Early rehabilitation reduces 1-year readmission rates.

Strong Rec High Evidence GOLD 2024
30

Provide a maintenance plan after the formal programme ends — home exercise prescription, community walking group, or repeat course at 12 months — otherwise gains fade by 12 months.

Moderate Rec Moderate Evidence NICE NG115
Clinical Pearl: The clinic that asks “Have you been referred to pulmonary rehab?” at every COPD visit converts more patients than the clinic that asks once. Make the referral a default, not an option.

Long-Term Oxygen Therapy: Strict Criteria, Real Mortality Benefit

Long-term oxygen therapy (LTOT) is the only pharmacological intervention apart from smoking cessation that improves survival in COPD — but only when the criteria are met. The LOTT trial established that patients with isolated moderate exertional desaturation do not benefit, narrowing the indication considerably.

31

Prescribe LTOT (target ≥ 15 hours daily) for patients with stable COPD and a resting PaO&sub2; ≤ 55 mmHg (7.3 kPa), or SpO&sub2; ≤ 88% confirmed on at least two occasions over 3 weeks.

Strong Rec High Evidence GOLD 2024
32

Extend LTOT eligibility to patients with PaO&sub2; 56–59 mmHg (or SpO&sub2; 89%) when accompanied by polycythaemia (haematocrit > 55%), peripheral oedema, or cor pulmonale.

Strong Rec Moderate Evidence GOLD 2024
33

Do not prescribe LTOT for moderate resting hypoxaemia alone (SpO&sub2; 89–93%) or for isolated exertional desaturation. The LOTT trial showed no benefit on mortality or first hospitalisation in this group.

Against High Evidence LOTT 2016
34

Consider ambulatory oxygen for selected patients with significant exertional desaturation who improve exercise tolerance with supplemental O&sub2; on a formal walk test — the indication is symptomatic, not mortality-based.

Conditional Rec Moderate Evidence NICE NG115
35

Counsel every patient on LTOT against smoking on home oxygen and arrange written fire-safety information. Active smokers on home oxygen carry a real risk of facial and airway burns.

Strong Rec Low Evidence NICE NG115
Clinical Pearl: Always reassess LTOT eligibility after a patient stops smoking, completes pulmonary rehabilitation, and is on optimised inhalers. Hypoxaemia sometimes improves enough to come off oxygen.

Clinical Decision Pathway

A practical, question-based pathway for a routine COPD review visit. Run through it in order.

Routine COPD Management Review: 6 Questions
Question 1: Is the diagnosis confirmed?
If no documented post-bronchodilator FEV1/FVC < 0.70 → arrange spirometry before any maintenance inhaler.
Question 2: What is the GOLD ABE group today?
Score CAT or mMRC + count exacerbations over the last 12 months.
Group A → LAMA (or LABA) monotherapy. Group B → LABA + LAMA. Group E → LABA + LAMA ± ICS based on eosinophils.
Question 3: Does this patient need ICS?
Eosinophils ≥ 300 cells/µL → yes, add ICS (triple therapy).
Eosinophils 100–299 cells/µL with ongoing exacerbations on LABA + LAMA → consider ICS.
Eosinophils < 100 cells/µL → avoid ICS; pneumonia risk outweighs benefit.
Question 4: Are the non-inhaler pillars in place?
Smoking status checked, cessation support offered if relevant.
Influenza, pneumococcal, COVID-19, RSV (≥ 60), Tdap all up to date.
Pulmonary rehabilitation referred if mMRC ≥ 2 or recent exacerbation.
Question 5: Is the patient still exacerbating despite triple therapy?
Recheck technique, adherence, and diagnosis first.
If genuinely refractory → consider roflumilast (FEV1 < 50%, chronic bronchitis) or chronic azithromycin (former smokers).
Question 6: Is oxygen indicated?
Resting SpO&sub2; ≤ 88% (or PaO&sub2; ≤ 55 mmHg) confirmed twice → LTOT, ≥ 15 h/day.
Resting SpO&sub2; 89% with cor pulmonale or polycythaemia → LTOT.
Moderate desaturation only (SpO&sub2; 89–93%) → no LTOT; consider ambulatory oxygen if symptomatic on testing.

Practical Reference Tables

Two reference tables for fast clinic use: inhaler classes organised by drug rather than by severity, and an eosinophil-based ICS decision grid.

Inhaler Classes in COPD Management: A Drug-by-Drug Guide

ClassExample Drug & DoseBest Used InPractical Tips
SABA (rescue)Salbutamol 100 µg, 1–2 puffs as neededAll patients, rescue onlyUse with a spacer when possible; rising frequency of use signals worsening control.
LAMATiotropium 18 µg once dailyGroup A monotherapy; component of LABA + LAMAAvoid in narrow-angle glaucoma; rinse mouth and watch for dry mouth.
LABAFormoterol 12 µg twice dailyAlternative monotherapy; component of LABA + LAMAWatch for tremor and tachycardia; reassess if palpitations.
LABA + LAMASingle-inhaler combination, once or twice dailyGroup B and Group E first lineSingle inhaler beats two separate devices for adherence.
Triple (LABA + LAMA + ICS)Once or twice daily depending on productGroup E with eosinophils ≥ 300 or ongoing exacerbationsMonitor for pneumonia, oral candidiasis; rinse mouth after use.
Roflumilast250 µg daily × 4 weeks, then 500 µg dailyFEV1 < 50%, chronic bronchitis, frequent exacerbationsCommon: nausea, diarrhoea, weight loss, mood change.
Chronic azithromycin250 mg daily or 500 mg 3×/weekFormer smokers with persistent exacerbationsBaseline ECG and audiometry; review at 12 months.

Eosinophil-Based ICS Decision Grid

Blood EosinophilsExacerbation HistoryICS RecommendationPractical Consideration
≥ 300 cells/µLAny (especially ≥ 1 mod or 1 hosp)Add ICS (triple therapy)Largest exacerbation reduction signal; benefit clearly outweighs pneumonia risk.
100–299 cells/µL≥ 2 moderate or 1 severeConsider ICSDiscuss trade-off; reassess at 6–12 months.
100–299 cells/µLNo exacerbationsDo not add ICSStay on LABA + LAMA; review annually.
< 100 cells/µLAnyAvoid ICSPneumonia risk likely outweighs any small exacerbation benefit.

Monitoring and Follow-Up

A simple schedule keeps long-term COPD management on track and catches problems before they become exacerbations.

ParameterWhen to CheckWhat to DoCommon Pitfalls
CAT or mMRC scoreEvery routine visitUse to reclassify ABE group and guide escalationForgetting to repeat — one-off scores miss trends
Exacerbation historyEvery routine visitCount moderate (oral steroids/antibiotics) and severe (admission)Under-reporting of home-managed exacerbations
Inhaler techniqueAt every visit and before any escalationObserve the patient using the device; correct technique on the spotAsking instead of watching — self-report overestimates skill
Blood eosinophilsAt diagnosis, before ICS decisions, after major status changeUse a stable-state value, ideally on > 1 occasionDrawing during an exacerbation or oral steroid course
SpO&sub2; at restEvery routine visit; before any oxygen decisionIf ≤ 92%, arrange formal ABG and reassessmentPrescribing LTOT off a single low reading without ABG confirmation
Vaccination statusAnnual reviewUpdate influenza, COVID-19; check pneumococcal, RSV, TdapAssuming hospital teams or pharmacies caught everything
Smoking statusEvery visitOffer cessation support; document attemptAsking once and not revisiting

Evidence in Context

What the trials show and where the major frameworks agree or differ.

Where GOLD 2024 and NICE NG115 Agree

Both frameworks agree on confirming COPD with post-bronchodilator spirometry, on a structured symptom plus exacerbation assessment at every visit, on smoking cessation as the highest-yield intervention, on routine influenza and pneumococcal vaccination, and on pulmonary rehabilitation for symptomatic patients and post-exacerbation. Both also support LABA + LAMA over LABA + ICS for most patients without an eosinophilic phenotype.

Where GOLD 2024 and NICE NG115 Differ

ABE classification: GOLD uses the ABE framework directly; NICE leans more on symptom burden plus exacerbation history without formally adopting ABE letters.

ICS decision: GOLD makes blood eosinophils a central, quantitative variable in the ICS decision; NICE places more weight on a history of asthma features or eosinophilia rather than thresholding strictly on a count.

Most everyday decisions converge despite the framing differences.

Triple Therapy: What the ETHOS and IMPACT Trials Showed

Both trials found that single-inhaler triple therapy reduced moderate-to-severe exacerbations compared with LABA + LAMA in patients with a history of exacerbations. Both signalled a mortality benefit that strengthened as eosinophil count rose, reinforcing the eosinophil-guided approach to ICS in COPD management.

Pneumonia rates were higher with ICS-containing arms, which underlines why ICS should be reserved for patients with the right phenotype rather than used routinely.

LOTT: Why Moderate Hypoxaemia Is No Longer an Oxygen Indication

The Long-Term Oxygen Treatment Trial randomised patients with stable COPD and moderate resting hypoxaemia (SpO&sub2; 89–93%) or isolated exertional desaturation to supplemental oxygen versus no oxygen. There was no difference in time to death or first hospitalisation. The trial reframed LTOT as a narrow intervention for severe resting hypoxaemia, not a generic add-on for marginal saturations.

Eosinophils: A Continuous Biomarker, Not a Switch

The 100 and 300 cells/µL cut-offs are pragmatic, not mechanistic. Pooled trial data show a smooth gradient: every step up in eosinophil count corresponds to a larger ICS-related exacerbation reduction. Treat the count as a guide to direction and magnitude of effect, not a binary on/off switch.

References

  1. 1.Global Initiative for Chronic Obstructive Lung Disease. Global Strategy for the Diagnosis, Management, and Prevention of Chronic Obstructive Pulmonary Disease — 2024 Report. Available at: goldcopd.org/2024-gold-report
  2. 2.National Institute for Health and Care Excellence. Chronic obstructive pulmonary disease in over 16s: diagnosis and management. NICE Guideline NG115. Last updated 2024. Available at: nice.org.uk/guidance/ng115
  3. 3.Rabe KF, Martinez FJ, Ferguson GT, et al. Triple Inhaled Therapy at Two Glucocorticoid Doses in Moderate-to-Very-Severe COPD. N Engl J Med. 2020;383(1):35–48. doi:10.1056/NEJMoa1916046
  4. 4.Lipson DA, Barnhart F, Brealey N, et al. Once-Daily Single-Inhaler Triple versus Dual Therapy in Patients with COPD. N Engl J Med. 2018;378(18):1671–1680. doi:10.1056/NEJMoa1713901
  5. 5.Long-Term Oxygen Treatment Trial Research Group. A Randomized Trial of Long-Term Oxygen for COPD with Moderate Desaturation. N Engl J Med. 2016;375(17):1617–1627. doi:10.1056/NEJMoa1604344
  6. 6.Singh D, Bafadhel M, Brightling CE, et al. Blood Eosinophil Counts in COPD: A Biomarker of Inflammation and Treatment Response. Lancet Respir Med. 2018;6(2):117–126. doi:10.1016/S2213-2600(18)30298-X

How to Read the Evidence Tags

Every recommendation in this article carries simplified Medaptly tags for recommendation strength, evidence quality, and source — intended as a fast read at the bedside, not as a substitute for the original source classification.

Recommendation Strength

TagWhat It Means
Strong RecHigh-quality evidence broadly supports this action.
Moderate RecThe weight of evidence favours this action.
Conditional RecBenefit is less certain — individualise.
AgainstEvidence shows no benefit or potential harm.

Evidence Quality

TagWhat It Means
High EvidenceMultiple well-designed RCTs or high-quality meta-analyses.
Moderate EvidenceSingle RCT or large observational studies.
Low EvidenceExpert consensus or small studies.

Article Information

For Educational Purposes Only. This is original clinical education content informed by current published guidelines and clinical evidence on COPD management. It does not constitute medical advice, is not endorsed by any guideline body, and does not replace individualised clinical judgement or local formulary guidance. Drug dosages and oxygen prescribing criteria should always be verified against current product information and local protocols before any clinical decision. Readers are encouraged to consult the original source guidelines listed in References.

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