Aspergillosis Research Highlights — Week in Review (Last 7 Days: Week 50)
Seven key publications: pathogenicity, diagnostics, resistance, treatment, maxillofacial disease, and ABPA in COPD.
1. Comparative Overview of A. fumigatus, A. flavus, and A. niger
Rafique et al., J Infect Public Health, 2025
DOI: 10.1016/j.jiph.2025.103070
What this adds
-
A major comparative review (2000–2025) of the three most clinically relevant Aspergillus species.
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Highlights broad clinical spectrum: allergy → chronic disease → invasive aspergillosis.
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Identifies species-specific concerns:
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A. fumigatus: globally dominant, rapidly evolving triazole resistance.
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A. flavus: important in warmer climates; high aflatoxin relevance.
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A. niger: relatively lower virulence but significant in sinus disease.
-
-
Public health message: surveillance gaps persist, especially for non-fumigatus species.
Why it matters
A strong reference paper supporting the WHO prioritisation of Aspergillus, and reinforcing the need for:
-
Better diagnostics
-
Species-level identification
-
Environmental resistance monitoring
2. GFP Fusion Protein Proteolysis in A. fumigatus
Paul & Moye-Rowley, G3 (Bethesda), 2025
DOI: 10.1093/g3journal/jkaf295
What this adds
-
Fundamental molecular biology study revealing regulated degradation pathways of green fluorescent protein (GFP) fusion proteins inside A. fumigatus.
-
Demonstrates how the fungus controls protein turnover under stress conditions.
Why it matters
-
Advances tools for fungal cell biology.
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Supports drug development by clarifying pathways involved in stress response and antifungal tolerance.
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Reinforces WHO’s classification of A. fumigatus as one of the four most critical fungi to study.
3. ABPA in COPD: Case Series + Review
Ren et al., BMC Pulmonary Medicine, 2025
DOI: 10.1186/s12890-025-04027-8
What this adds
-
11 COPD cases with confirmed Allergic Bronchopulmonary Aspergillosis — highlighting:
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Under-recognition in COPD
-
Overlap with chronic bronchitis/bronchiectasis symptoms
-
Frequent misdiagnosis as recurrent infections or COPD exacerbations
-
-
Provides diagnostic guidance and a literature synthesis.
Why it matters
-
Significant implications for case finding across the UK.
-
Supports NAC messaging: ABPA is not only an asthma disease.
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Reinforces need for:
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IgE/IgG screening
-
Early CT imaging
-
Awareness among COPD teams and primary care
-
4. EL219: Next-Generation Polyene Antifungal
Youssef et al., AAC, 2025
DOI: 10.1128/aac.01400-25
What this adds
-
Animal model evidence that EL219, a modern polyene, is effective against:
-
Triazole-susceptible A. fumigatus
-
Azole-resistant isolates
-
Difficult species (A. lentulus, A. calidoustus)
-
Why it matters
-
Highly relevant to rising global antifungal resistance.
-
Early indication that EL219 may fill a clinical gap similar to (or complementary to) olorofim and fosmanogepix.
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Suggests strong activity even in immunosuppressed models.
5. Misidentification & Triazole Resistance in Aspergillus tubingensis
Wang et al., JAMA Network Open, 2025
DOI: 10.1001/jamanetworkopen.2025.43630
What this adds
-
Large Southern California population study showing:
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Frequent misidentification of A. tubingensis as A. niger.
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Notable azole resistance rates in correctly identified isolates.
-
-
Stresses need for genomic sequencing or MALDI-TOF with updated libraries.
Why it matters
-
Strong evidence that misidentification leads to:
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Inappropriate antifungal therapy
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Poor outcomes
-
-
Supports calls for expanded diagnostic reference services such as MRCM.
6. 50-Year Review of Oral Fungal Infections in Thailand
Kosanwat et al., Clinical Oral Investigations, 2025
DOI: 10.1007/s00784-025-06685-8
What this adds
-
Longitudinal study: 29% of deep infections involved aspergillosis.
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Mean age 62 → older adults most affected.
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Many cases were mucormycosis, histoplasmosis, or aspergillosis presenting late.
Why it matters
-
Shows that oral/maxillofacial fungal disease remains under-recognised globally.
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Relevant to dental teams → better imaging + biopsy protocols needed.
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May help NAC/CARES identify referral pathways from dental medicine.
7. Management of Maxillary Sinus Aspergillosis with Implants
Khoury et al., Int J Oral Implantol, 2025
What this adds
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Real-world 3–10 year follow-up of 11 patients.
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Standardised approach:
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Surgical clearance
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Antifungal therapy
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Successful implant-prosthetic rehabilitation
-
Why it matters
-
Demonstrates excellent long-term outcomes when sinus aspergillosis is properly treated.
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Practical implications for:
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ENT surgeons
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Oral surgeons
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Implant dentistry
-
-
Supports inclusion of aspergillosis in sinus disease differential diagnosis.
Cross-Cutting Themes Emerging This Week
1. Under-recognition and misidentification
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ABPA in COPD
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Misidentified A. tubingensis
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Asymptomatic sinus disease
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Oral/maxillofacial deep fungal infections
→ Key NAC message: We are missing cases in primary care, COPD clinics, ENT, and dentistry.
2. Antifungal resistance remains a central threat
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Contemporary reviews of species-specific resistance patterns
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EL219’s promise against resistant species
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Misidentification leading to incorrect susceptibility assumptions
3. Need for better diagnostics and reference centres
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Species-level identification is essential
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Supports arguments for expansion of MRCM-style national services
4. The clinical spectrum is broad
From allergy (ABPA in COPD) → chronic sinus disease → deep oral infections → invasive pulmonary aspergillosis.
This reinforces the message: aspergillosis is multi-specialty, not confined to respiratory medicine.
Weekly NAC/MRCM Take-Home Messages
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COPD teams should screen for ABPA more frequently—especially in patients with recurrent “infective exacerbations.”
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Species-level identification is increasingly important; misidentification contributes to treatment failure.
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New antifungals like EL219 show promise against resistant strains including A. lentulus.
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Dental and ENT teams need better awareness: sinus and oral fungal infections remain overlooked but treatable.
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Global reviews show growing public health significance of Aspergillus species—aligning with WHO priorities.
⭐ Severe Asthma with Fungal Sensitisation (SAFS): The Hidden Burden Behind Difficult Asthma
Estimated prevalence: 15–30% of severe asthma patients show fungal sensitisation.
Severe Asthma with Fungal Sensitisation (SAFS) describes a group of patients with severe asthma who show sensitisation (allergy) to Aspergillus or other environmental moulds but do not meet criteria for ABPA. These patients often experience persistent inflammation, breathlessness, mucus production, and exacerbations that are not adequately controlled by standard asthma therapies.
Although SAFS is common in severe asthma clinics, it remains poorly recognised, frequently mislabelled, and rarely discussed in routine practice. Yet identifying SAFS is crucial because it opens the door to specific interventions — including antifungals or targeted biologics — that can improve symptoms and reduce hospital admissions.
⭐ How Common Is SAFS?
SAFS is more common than ABPA and CPA combined in asthma services.
| Population | Estimated prevalence |
|---|---|
| Moderate asthma | ~5% |
| Severe asthma | 15–30% |
| Patients with frequent exacerbations | up to 40% |
| ABPA-negative patients with mucus plugging | high likelihood |
Across the UK, this represents tens of thousands of people.
⭐ Why SAFS Is Missed
1. The diagnosis is not widely understood
Unlike ABPA or CPA, SAFS lacks:
-
universally agreed diagnostic criteria
-
clear imaging features
-
a single confirmatory test
This leads to variability in thinking and detection.
2. Symptoms mimic uncontrolled asthma
SAFS patients typically experience:
-
severe breathlessness
-
wheeze
-
mucus production
-
airway plugging
-
poor response to inhalers
-
frequent steroid courses
These appear indistinguishable from “difficult” or “type 2–high” asthma.
3. IgE and eosinophils may be normal
Unlike ABPA:
-
total IgE may be modest
-
Aspergillus IgE may be borderline
-
eosinophils may fluctuate, especially with steroids or biologics
Clinicians are often looking for very high IgE levels — but SAFS patients usually don’t show them.
4. Sputum and CT scans appear non-specific
Typical imaging:
-
mucus plugging
-
small-airway thickening
-
variable, patchy inflammation
-
bronchiectasis may or may not be present
Radiologists often report these changes as:
-
“consistent with asthma”
-
“post-infective”
-
“non-specific inflammatory pattern”
5. The fungal link is overlooked
Many clinicians are unfamiliar with:
-
the role of mould exposure
-
sensitisation thresholds
-
the overlap between environmental allergy and airway disease
-
when antifungals are appropriate
This leads to delays in recognising fungal-driven asthma.
⭐ Who Is at Highest Risk?
1. Severe asthma patients unresponsive to maximal inhaled treatment
Particularly those with:
-
frequent exacerbations
-
nocturnal symptoms
-
long-term steroid use
-
persistently low lung function
-
mucus plugging events
2. Patients sensitised to Aspergillus or multiple moulds
Positive skin tests or specific IgE indicate airway allergy that can drive symptoms.
3. Patients with damp or mould exposure at home or work
An important environmental factor often overlooked.
4. ABPA-negative asthma patients with mucus plugging
A large proportion of these patients fit the SAFS profile.
5. Those with co-existing bronchiectasis
Bronchiectasis amplifies the inflammatory response to fungal exposure.
⭐ Specialties That Need Greater Awareness
-
Severe asthma services & biologics clinics
(primary diagnostic opportunity) -
General respiratory clinics
-
Primary care & urgent care
(patients seen frequently with “persistent asthma symptoms”) -
Radiology
(important for identifying mucus plugging) -
Allergy/Immunology
(mould sensitisation is central to diagnosis) -
Environmental health teams
(exposure to mould and dampness often perpetuates symptoms)
The National Aspergillosis Centre can provide specialist input when diagnosis is unclear or response to treatment is suboptimal.
⭐ Red Flags Suggesting SAFS
1. Severe asthma poorly controlled despite maximal inhalers
Including biologics (omalizumab, mepolizumab, benralizumab, dupilumab, tezepelumab).
2. Sensitisation to Aspergillus fumigatus or multiple moulds
3. Repeated mucus plugging episodes
(or “sticky mucus” symptoms)
4. More than 2–3 steroid-treated exacerbations per year
5. Asthma + bronchiectasis
Even mild bronchiectasis increases fungal risk.
6. Symptoms triggered by damp/mould exposure
7. Persistent airway inflammation despite correct inhaler technique
⭐ Misdiagnoses That Delay Recognition
-
“Difficult asthma”
-
“Brittle asthma”
-
“Post-viral inflammation”
-
“Poor adherence to inhalers”
-
“Asthma–COPD overlap”
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“Psychogenic dyspnoea”
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“Recurrent chest infections”
SAFS is a diagnosis hiding in these labels.
⭐ The Cost of Missed SAFS Diagnosis
For patients:
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persistent symptoms
-
steroid dependence
-
increased risk of ABPA
-
progressive airway damage
-
hospital admissions
-
poor quality of life
-
possible career and lifestyle impact
For healthcare systems:
-
repeated A&E visits
-
asthma admissions
-
high biologic usage without adequate response
-
unnecessary antibiotics
-
escalating steroid toxicity
-
missed environmental interventions
⭐ Conclusion
SAFS is one of the most common — yet least recognised — fungal-related lung conditions. Although it lacks the dramatic imaging changes of ABPA or CPA, its impact on patients is profound.
Recognising mould sensitisation in severe asthma, understanding the role of fungal allergens, and considering targeted therapies can transform disease control. For complex cases or when the diagnosis is uncertain, referral to the National Aspergillosis Centre is recommended.
Early identification and appropriate treatment reduce steroid use, exacerbations, and long-term airway damage.
⭐ Aspergillus Bronchitis: The Overlooked Condition Hiding in Plain Sight
Estimated prevalence 1–2% in bronchiectasis and chronic airway disease clinics.
Aspergillus Bronchitis (AB) is a chronic, symptomatic infection of the airways caused by Aspergillus species in people with underlying lung disease. It sits between simple colonisation and chronic pulmonary aspergillosis (CPA), and is frequently overlooked or mislabelled as “recurrent infection,” “post-viral symptoms,” or uncontrolled bronchiectasis.
Unlike CPA, Aspergillus Bronchitis does not require cavities or major structural destruction — which makes it both easier to miss and surprisingly common among people with chronic airway disease.
When recognised and treated (usually with antifungal therapy for several months), symptoms often improve significantly. But because awareness remains low, most patients cycle through unnecessary antibiotics, repeated exacerbations, and worsening airway disease before the real cause is identified.
⭐ What Exactly Is Aspergillus Bronchitis?
Aspergillus Bronchitis is defined by:
-
chronic productive cough
-
sputum growing Aspergillus species repeatedly
-
airway inflammation
-
symptoms lasting over 3 months
-
underlying airway disease (bronchiectasis, CF, COPD, prior TB, ABPA)
-
response to antifungal therapy
Unlike ABPA:
-
there is no allergic response,
-
IgE is usually normal,
-
eosinophils are normal or mildly elevated.
Unlike CPA:
-
there are no cavities on imaging,
-
IgG may be normal or only slightly elevated,
-
disease is confined to the airways, not lung tissue.
This places AB in a “grey zone” — often invisible unless specifically looked for.
⭐ Why Aspergillus Bronchitis Is Missed
1. Symptoms mimic common chronic airway disease
Typical AB symptoms include:
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daily productive cough
-
worsening sputum thickness
-
breathlessness
-
fatigue
-
repeated “chest infections”
-
slow-to-clear mucus
-
crackles or wheeze
These resemble:
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bronchiectasis exacerbations
-
COPD flare-ups
-
chronic infection with Pseudomonas or NTM
-
post-viral cough
-
uncontrolled asthma
Without fungal awareness, clinicians default to bacterial explanations.
2. Sputum grows multiple organisms — Aspergillus is dismissed
In bronchiectasis, sputum frequently grows:
-
Haemophilus
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Pseudomonas
-
Staphylococcus
-
Streptococcus
-
NTM
When Aspergillus appears, it’s often labelled:
-
“colonisation”
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“contaminant”
-
“not clinically relevant”
But repeated isolation with persistent symptoms is highly suggestive of AB.
3. IgE/IgG results may be normal
Many clinicians expect high IgE or IgG to “confirm Aspergillus disease.”
But in Aspergillus Bronchitis:
-
IgE is usually normal
-
IgG can be normal or borderline
This leads to false reassurance.
4. Radiology rarely shows overt features
CT scans in AB may show:
-
mucus plugging
-
mild bronchial wall thickening
-
small nodules
-
progression of bronchiectasis
But they do not show the cavities of CPA or classic features of ABPA.
Therefore radiologists often report scans as “no significant change” or “stable bronchiectasis.”
5. Antibiotics appear to help — temporarily
Patients often improve slightly with:
-
amoxicillin
-
doxycycline
-
macrolides
-
ciprofloxacin
This gives clinicians the impression of bacterial disease, but symptoms soon return.
6. Lack of awareness
Many specialists (even in respiratory clinics) are unaware that Aspergillus Bronchitis:
-
exists as a distinct clinical entity
-
can be disabling
-
responds to antifungals
-
predicts progression to CPA if untreated
This leads to significant diagnostic delay.
⭐ Who Is at Highest Risk?
1. Bronchiectasis
The largest risk group.
Aspergillus Bronchitis may account for 1–2% of all bronchiectasis patients, and up to 5–10% in severe or frequent exacerbator groups.
2. Cystic Fibrosis (CF)
These patients frequently grow Aspergillus but not all have ABPA — some have Aspergillus Bronchitis.
3. COPD and chronic productive cough
Especially those with:
-
frequent mucus plugging
-
repeated “infective exacerbations”
-
progressive sputum production
4. Post-TB airway damage
Chronic airway deformity, scarring, and bronchiectasis from old TB predispose to fungal infection.
5. Post-COVID structural disease
A new and growing risk group, especially after prolonged ICU ventilation.
6. ABPA patients
Some patients develop Aspergillus Bronchitis during steroid-dominated treatment or after stopping antifungals.
⭐ Which Specialities Need Greater Awareness?
-
Respiratory medicine
(especially bronchiectasis clinicians and severe asthma teams) -
Infectious Diseases
(frequent respiratory presentations with chronic airway infection) -
Radiology
(to recognise subtle but progressive airway changes) -
Primary care
(“recurrent chest infection” or “persistent cough” patients) -
Physiotherapy & airway clearance teams
(excessive sputum with fungal elements) -
Cystic Fibrosis services
The National Aspergillosis Centre is the ideal referral destination when diagnosis is uncertain or symptoms persist despite typical management.
⭐ Red Flags Suggesting Aspergillus Bronchitis
1. Chronic (>3 months) productive cough + repeated Aspergillus in sputum
Even 2 positive sputums in the right clinical context should raise suspicion.
2. Bronchiectasis patient not improving on repeated antibiotics
3. Thick, tenacious mucus with black, grey, or brown plugs
4. Worsening CT bronchiectasis or mucus plugging
5. Absence of features typical for ABPA (normal IgE, no fleeting infiltrates)
6. Asthma or COPD patient with new persistent sputum
7. Partial response to antibiotics but rapid relapse
8. Unexplained fatigue and breathlessness in someone with airway disease
⭐ The Cost of Missed Aspergillus Bronchitis
If AB is not recognised early, consequences include:
-
repeated exacerbations
-
accelerating bronchiectasis
-
long-term airway damage
-
chronic inflammation
-
steroid overuse
-
unnecessary antibiotics
-
repeated hospitalisations
-
progression to CPA in some patients
For health systems, missed diagnosis leads to:
-
higher admission rates
-
inappropriate long-term antibiotic use
-
avoidable CT scans and investigations
-
greater long-term burden of CPA
But antifungal therapy — when appropriately used — can offer marked symptom improvement and reduce exacerbation frequency.
⭐ Conclusion
Aspergillus Bronchitis is a distinct, treatable form of chronic airway disease seen in people with bronchiectasis, asthma, COPD, CF, and post-TB lung damage. Yet lack of awareness means many patients are repeatedly misdiagnosed with bacterial infections or unexplained chronic cough.
Recognising red flags, reviewing sputum results carefully, and considering antifungal therapy can dramatically improve outcomes. Early referral to specialist centres such as the National Aspergillosis Centre is recommended for complex cases or uncertain diagnosis.
Early identification prevents airway deterioration — and reduces the likelihood of progression to CPA.
⭐ Allergic Bronchopulmonary Aspergillosis (ABPA): Why Diagnosis Is Missed and Who Needs to Be More Aware
With estimated prevalence of 1–2% in asthma clinics and up to 10% in severe asthma services.
Allergic Bronchopulmonary Aspergillosis (ABPA) is a chronic immune reaction to Aspergillus that affects people with asthma or cystic fibrosis. It causes airway inflammation, mucus plugging, recurrent exacerbations, and bronchiectasis if untreated.
Despite being treatable, ABPA remains heavily underdiagnosed, even in countries with advanced respiratory services. Many people are told for years that they have “difficult asthma” or “recurrent chest infections,” only for ABPA to be diagnosed much later, often with significant lung damage already present.
The UK National Aspergillosis Centre (NAC) provides specialist expertise, yet only a small proportion of expected ABPA cases reach specialist review.
This article explains why ABPA is missed, which patients are at risk, which specialities need to be more alert, and the red flags that should prompt testing or referral.
⭐ How Common Is ABPA?
ABPA is more common than most clinicians realise:
| Population | Estimated prevalence |
|---|---|
| General asthma | 1–2% |
| Severe asthma clinics | 3–10% |
| Cystic fibrosis | 5–15% |
| Bronchiectasis (non-CF) | 1–4% |
Across the UK, this equates to an estimated 15,000–25,000 people living with ABPA — but only a small minority ever receive the correct diagnosis.
⭐ Why ABPA Is Often Missed
1. ABPA looks like “difficult asthma”
Typical symptoms — wheeze, cough, mucus, breathlessness — mimic:
-
severe asthma
-
eosinophilic asthma
-
uncontrolled asthma despite treatment
Patients may be repeatedly stepped up through inhalers, oral steroids, and biologics before ABPA is even considered.
2. Exacerbations are mistaken for infections
Many ABPA flare-ups are treated as:
-
pneumonia
-
viral infection
-
“chest infection”
-
post-viral asthma worsening
Without fungal-specific thinking, the diagnosis is rarely made.
3. IgE and eosinophils fluctuate
IgE is a cornerstone of ABPA diagnosis, but:
-
systemic steroids suppress IgE
-
biologics (benralizumab, mepolizumab, dupilumab) reduce eosinophils
-
flare-ups produce temporary spikes
-
baseline ranges vary between labs
Clinicians often overlook ABPA in patients on biologics because eosinophils are normal — despite the underlying fungal allergy still being active.
4. Radiology findings get mislabelled
ABPA causes:
-
mucus plugging
-
“tram lines” and bronchial thickening
-
fleeting infiltrates
-
upper lobe bronchiectasis
These are often:
-
labelled “infection”
-
attributed to asthma airway remodelling
-
not compared across time
-
missed on CT unless specifically looked for
5. Inconsistent awareness across specialities
Some clinicians are unfamiliar with:
-
ISHAM diagnostic criteria
-
interpreting IgE/IgG results
-
the relationship between asthma and fungal allergy
-
the overlap between ABPA and bronchiectasis
This leads to diagnostic delay or misdiagnosis.
6. ABPA evolves into chronic disease if untreated
Repeated inflammation → mucus plugging → bronchiectasis → fibrosis.
By the time a diagnosis is made, airway damage can be permanent.
⭐ Who Is at Highest Risk?
1. Asthma patients with repeated exacerbations
Especially those who:
-
fail maximal inhaler therapy
-
require multiple steroid courses
-
have sudden, dramatic mucus plugging events
-
experience episodic “flares” with no clear cause
2. Severe asthma clinic patients
Prevalence is up to 10%, especially those with:
-
high IgE
-
eosinophilia
-
sensitisation to multiple allergens
-
steroid dependence
3. Bronchiectasis patients
Bronchiectasis often coexists with ABPA and can worsen flares.
4. Patients with mucus plugging (“finger-in-glove” signs)
These striking CT appearances strongly suggest ABPA but are often misattributed to infection.
5. People with CF (Cystic Fibrosis)
5–15% develop ABPA at some stage.
⭐ Which Specialities Need Greater Awareness?
-
Severe asthma services & biologics clinics
(highest yield group for ABPA detection) -
Respiratory medicine
(diagnosis often falls here but is highly variable) -
General practice
(sees frequent “exacerbations”) -
Emergency departments & acute medical units
(manage acute mucus plugging, chest tightness) -
Paediatric respiratory medicine
(early recognition prevents chronic damage) -
Cystic Fibrosis services
-
Radiology
(fleeting infiltrates and mucus plugging often give the earliest clues)
The National Aspergillosis Centre should be the referral point for complex or uncertain cases.
⭐ Red Flags Suggesting ABPA
1. Asthma with repeated, unexplained exacerbations
Especially if poorly responsive to normal treatment.
2. High total IgE (>500–1000 IU/mL)
Or rising IgE over time.
3. Eosinophilia (unless suppressed by treatment)
4. Positive Aspergillus sensitisation
(Skin prick test or specific IgE)
5. Bronchiectasis, particularly central or upper lobe
6. Fleeting pulmonary infiltrates
7. Mucus plugging on CT (“finger-in-glove” appearance)
8. ABPA flare triggered by stopping antifungals
9. Asthma + Aspergillus in sputum
⭐ The Cost of Missed ABPA Diagnosis
Failure to diagnose ABPA leads to:
-
progressive airway damage
-
permanent bronchiectasis
-
steroid dependence
-
hospital admissions
-
repeated infections
-
respiratory failure in advanced stages
-
reduced quality of life
-
avoidable healthcare expenditure
Delayed diagnosis increases the risk of progression to CPA, a far more serious chronic fungal infection requiring long-term antifungal therapy.
Early recognition, correct treatment, and referral to specialist centres like the National Aspergillosis Centre dramatically improve long-term outcomes.
⭐ Conclusion
ABPA is not rare — especially within severe asthma clinics, bronchiectasis services, and CF units. Yet it remains significantly underdiagnosed because its symptoms mirror those of common respiratory conditions, and because key investigations like IgE, IgG, and CT interpretation are inconsistently used.
A structured approach — recognising red flags, performing appropriate testing, and referring complex cases to the National Aspergillosis Centre — can reduce the burden of avoidable airway damage and improve the lives of thousands of patients.
⭐ Chronic Pulmonary Aspergillosis: Why Diagnosis Is Missed and Who Needs to Be More Aware
With estimated prevalence of 3–4 cases per 100,000 population, and far higher rates in high-risk groups.
Chronic Pulmonary Aspergillosis (CPA) is a slowly progressive fungal lung disease affecting an estimated 3–4 per 100,000 people in the UK, with higher estimates in global settings with greater TB prevalence. Despite this, many clinicians will go through entire careers without confidently recognising it — not because it is extremely rare, but because it almost always hides inside other long-term lung diseases.
The UK is unusual in having a nationally commissioned specialist service — the National Aspergillosis Centre (NAC), based at Wythenshawe Hospital, Manchester — offering funded diagnostics, multidisciplinary review, and long-term antifungal management. But only a fraction of expected CPA cases are ever referred. Most are simply never diagnosed.
This article explains why diagnoses are missed, who is at highest risk, which specialities need to be more alert, and the red flags that should trigger testing or referral.
⭐ How Common Is CPA? The Numbers Behind the Problem
The UK prevalence is estimated at 3–4 per 100,000 people — approximately 2,000–2,500 people with CPA at any given time.
But the risk is far higher in specific groups:
| Risk Group | Estimated CPA prevalence |
|---|---|
| Post-TB lung disease | 6–10% in those with residual cavities |
| Severe COPD (GOLD III–IV) | 1–3% |
| Bronchiectasis | 1–3% |
| NTM disease | 3–10% |
| Sarcoidosis with fibrosis | 1–2% |
| Immunosuppression (steroids/biologics) | Unknown, but rising |
Using these figures, the true UK caseload could exceed 4,000–6,000 individuals, yet NAC receives ~500–1,000 referrals, highlighting a large diagnostic gap.
⭐ Why CPA Is So Often Missed
1. Symptoms mimic common chronic lung diseases
CPA presents with:
-
Persistent cough
-
Breathlessness
-
Fatigue
-
Weight loss
-
Recurrent “chest infections”
-
Haemoptysis
These overlap almost perfectly with:
-
COPD
-
bronchiectasis
-
post-TB changes
-
long COVID
-
NTM infection
-
repeatedly “slow to clear” pneumonia
Because symptoms are non-specific, clinicians rarely think fungal.
2. Interpretation of imaging is inconsistent
CPA shows:
-
one or more cavities
-
pleural thickening
-
nodules
-
progressive changes over months
-
fungal balls
Common reporting pitfalls:
-
labelled “post-infective scarring”
-
misinterpreted as malignancy
-
seen but not compared longitudinally
-
incidental CT findings not acted upon
Radiology is one of the biggest missed opportunities for early detection.
3. IgG testing is not routinely requested
Aspergillus IgG is the key diagnostic biomarker — but it is:
-
often confused with IgE
-
not available in some hospitals
-
omitted from workups for recurrent infection
-
unfamiliar to non-respiratory clinicians
Without IgG, CPA is rarely diagnosed.
4. Short-term improvement with antibiotics is misleading
Patients with CPA may temporarily feel better after:
-
broad-spectrum antibiotics
-
steroids
-
physiotherapy
This transient improvement creates false reassurance.
5. CPA spans multiple specialisms — and no one owns it
Diagnosis requires combined expertise across:
-
respiratory medicine
-
infectious diseases
-
radiology
-
microbiology
-
immunology
When no one speciality takes responsibility, patients get lost.
⭐ Which Patients Are at High Risk?
CPA almost always develops on a background of existing lung damage.
1. Post-TB lung disease (PTLD)
Globally the largest CPA population.
Residual cavities are the strongest predictor.
Specialities needing awareness:
-
TB teams
-
ID physicians
-
Radiologists
-
Community TB nurses
-
Public health TB programmes
2. COPD (especially severe / emphysema)
Millions of people are potentially at risk.
Recurrent infections + bullae/cavities = fertile ground for CPA.
Specialities:
-
COPD clinics
-
Pulmonary rehab
-
Acute medicine (frequent admissions)
3. Bronchiectasis
Damaged airways enable persistent Aspergillus colonisation and inflammation.
Specialities:
-
Bronchiectasis MDTs
-
Severe asthma & NTM clinics
-
Respiratory physiotherapy
4. Sarcoidosis and ILD
Fibrosis and traction bronchiectasis develop cavities over time.
5. Post-COVID or post-influenza structural disease
Emerging risk group, especially in patients with:
-
ventilatory lung injury
-
persistent CT abnormalities
-
chronic steroid exposure
6. Chronic steroid or immunomodulator use
While invasive aspergillosis is linked to profound immunosuppression, CPA often affects those with milder, chronic immune dysfunction:
-
systemic steroids
-
high-dose inhaled steroids
-
biologics affecting eosinophils
-
poorly controlled diabetes
-
chronic kidney disease
-
malnutrition
⭐ Which Specialities Need to Be More Alert?
-
Respiratory Medicine – primary detection, but awareness varies greatly
-
Infectious Diseases – especially post-TB and persistent infection clinics
-
Radiology – key to spotting early changes
-
Primary Care – sees patients repeatedly with “ongoing chest infections”
-
Emergency & acute medicine – haemoptysis presentations
-
Bronchiectasis and NTM services – strong overlap
-
Severe asthma and biologics teams – ABPA → CPA evolution
-
TB clinics – highest prevalence globally, often least recognised
The National Aspergillosis Centre should be the referral point for any complex or uncertain case.
⭐ Red Flags: When to Suspect CPA
1. Cavities on CT (thin-, thick-walled, evolving, or multiple)
Especially with pleural thickening.
2. Haemoptysis
CPA is one of the most common causes of haemoptysis in people with cavities.
3. Symptoms lasting >3 months
Chronic cough, fatigue, weight loss, breathlessness.
4. “Recurrent infections” that never fully resolve
5. Post-TB patient with any new or worsening symptoms
6. Bronchiectasis patient with new cavity or Aspergillus culture
7. High or rising Aspergillus IgG
8. ABPA patient who deteriorates off antifungals
⭐ The Cost of Missed Diagnoses
When CPA is not recognised early, the consequences are severe:
-
irreversible lung damage
-
repeated hospitalisations
-
emergency haemoptysis events
-
prolonged antifungal therapy with more toxicity
-
reduced quality of life
-
avoidable deaths
For systems like the NHS, late diagnosis increases costs:
-
unplanned admissions
-
repeated CT imaging
-
prolonged antibiotics
-
intensive care during haemoptysis
-
complex surgery (lobectomy/pneumonectomy)
Early referral to specialist centres like the National Aspergillosis Centre prevents many of these harms.
⭐ Conclusion
CPA is not rare within the populations most likely to develop it.
Missed diagnoses are common, predictable, and preventable.
By increasing awareness across Respiratory, Infectious Diseases, Radiology, Primary Care, TB services, and severe asthma pathways — and by using simple tools such as Aspergillus IgG and careful CT interpretation — clinicians can dramatically reduce the diagnostic delay that damages lungs, quality of life, and survival.
The UK is fortunate to have the National Aspergillosis Centre as a nationally commissioned referral service. Recognising CPA early and referring appropriately has the power to save lives, reduce system costs, and improve long-term outcomes.
🌐 Promoting the NHS National Aspergillosis Centre (NAC)
Nationally Commissioned Service • Specialist Advice • Remote MDT • Patient Support
Chronic and allergic aspergillosis remain significantly under-recognised across the UK — despite their substantial burden on respiratory, infectious disease, and immunology services.
As the NHS England–commissioned National Aspergillosis Centre (NAC), based at Wythenshawe Hospital (Manchester University NHS Foundation Trust), we provide national expertise, remote support, and shared-care pathways for clinicians managing these complex conditions.
📊 Why This Matters
Chronic pulmonary aspergillosis (CPA) affects an estimated 3–4 per 100,000 people in the UK, with far higher rates in those with:
-
Previous tuberculosis
-
COPD
-
Non-tuberculous mycobacterial (NTM) lung disease
-
Sarcoidosis
-
Bronchiectasis
Allergic bronchopulmonary aspergillosis (ABPA) may affect:
-
2.5% of adult asthmatics
-
Up to 15% of people with cystic fibrosis
Yet both conditions are frequently undiagnosed or misdiagnosed, leading to delayed treatment and avoidable morbidity.
🏥 How NAC Supports Clinicians Across the UK
As the nationally commissioned centre for chronic aspergillosis, we offer:
🩺 Specialist clinical care
Face-to-face and remote clinics with structured long-term follow-up in partnership with local teams.
👥 National Aspergillosis MDT via Teams Remote Communication
A dedicated MDT where clinicians can refer and discuss complex diagnostic or therapeutic cases.
📧 Consultant-led advice & guidance
Available via phone & email, including:
-
Diagnostic support
-
Interpretation of IgE/IgG and fungal microbiology
-
Antifungal prescribing advice
-
Case planning for ABPA, CPA, SAFS and Aspergillus bronchitis
🔬 Access to advanced diagnostics
Including Aspergillus-specific IgE/IgG, culture, imaging, and molecular testing (e.g. antifungal resistance).
💬 Patient support & education (NAC CARES)
Moderated online groups, weekly patient meetings, webinars, and comprehensive educational resources — helping patients understand their condition and remain safely supported close to home.
🤝 We Welcome Collaboration
We’d be pleased to connect with respiratory, ID, immunology, and internal medicine teams to discuss:
-
Shared-care pathways
-
Diagnostic support
-
Service guidance
-
Virtual or in-person educational sessions
-
Case-specific MDT referrals
📄 Further information
Referral pathways, service scope and patient resources:
👉 https://mft.nhs.uk/wythenshawe/services/infectious-diseases/national-aspergillosis-centre/
Dr Chris Kosmidis
Clinical Lead, NHS National Aspergillosis Centre
Manchester University NHS Foundation Trust
**Adrenal Insufficiency & Steroid Tapering:
A Complete Patient Guide**
People taking long-term steroids (prednisolone, methylprednisolone, hydrocortisone, dexamethasone) can develop adrenal insufficiency because their adrenal glands “go to sleep” and stop making cortisol.
During tapering, the body must slowly “wake up” again — and this needs careful monitoring.
This guide explains the symptoms, tests, warning signs, and emergency precautions to keep you safe.
⭐ 1. Why adrenal insufficiency happens
Long-term steroid use suppresses the HPA axis (hypothalamus–pituitary–adrenal system).
When daily steroid doses are reduced, your body must produce more of its own cortisol. This takes time.
If the steroid reduction is too quick, or the body is under stress, low cortisol symptoms appear.
⭐ 2. Symptoms to watch for during steroid tapering
These are early signs that your body may not be keeping up with the reduction.
✔ Early, mild symptoms
-
Fatigue / sudden exhaustion
-
Muscle weakness
-
Dizziness when standing
-
Nausea or reduced appetite
-
Flu-like aching
-
Low mood, anxiety, irritability
-
Brain fog
-
Feeling unusually cold
-
Worsening joint or muscle pain
These often improve if the taper is slowed or paused.
⭐ 3. More serious symptoms of low cortisol
These symptoms suggest steroid levels are too low and the taper needs urgent review:
-
Vomiting
-
Persistent dizziness
-
Very low blood pressure
-
Severe fatigue (unable to function normally)
-
Salt cravings
-
Ongoing nausea preventing eating
-
Faintness or near-collapse
These require medical advice (same day).
⭐ 4. Emergency symptoms — possible adrenal crisis
Call 999 or go to A&E immediately if you develop:
-
Severe vomiting or diarrhoea
-
Collapse or inability to stand
-
Severe dehydration
-
Confusion
-
Sudden severe abdominal or back pain
-
Pale, clammy skin
-
Rapid breathing
-
Loss of consciousness
This is a medical emergency.
Patients normally receive 100 mg hydrocortisone IM/IV, but patients allergic to hydrocortisone require a pre-agreed emergency alternative — your endocrinologist must document this clearly.
⭐ 5. Symptoms that mean you may need a temporary “stress dose” of steroids
Your cortisol requirement increases during physical stress.
If you have adrenal suppression, your body cannot produce this extra cortisol.
You may need a temporary increase in dose if you have:
✔ Illness
-
Fever
-
Chest infection
-
Flu-like illness
-
COVID
-
Urinary infection
-
Gastroenteritis
-
Diarrhoea
-
Persistent nausea
✔ Physical stress
-
Injury
-
Significant fall
-
Severe pain
-
Dental surgery
-
Medical or surgical procedures
✔ Emotional stress
-
Bereavement
-
Panic attacks
-
Trauma
If vomiting prevents taking steroids → seek emergency help immediately.
⭐ 6. Tests used to monitor adrenal function during tapering
Doctors rely on a combination of symptoms and laboratory tests.
✔ Morning cortisol (8–9 am)
A key test to assess recovery.
Typical interpretation:
-
> 400–500 nmol/L → likely normal function
-
150–350 nmol/L → recovering / borderline
-
< 100 nmol/L → adrenal insufficiency
(Exact thresholds vary.)
✔ ACTH level
Shows whether the pituitary is trying to stimulate the adrenals.
-
Low ACTH → still suppressed
-
High ACTH → trying to wake adrenals
-
Normal ACTH + low cortisol → gland slow to respond
✔ Short Synacthen Test (SST)
Gold standard.
A small ACTH injection tests whether your adrenal glands can produce cortisol.
Used when:
-
taper reaches low doses
-
symptoms appear
-
deciding if steroids can be stopped
✔ Electrolytes (U&Es)
Low cortisol may cause:
-
Low sodium
-
High potassium (less common in steroid-induced insufficiency)
✔ Blood pressure monitoring
Low cortisol → low BP, dizziness, faintness.
✔ Glucose levels
Low-normal glucose and shakiness may occur during withdrawal.
✔ Clinical symptom review
Symptoms are sometimes more sensitive than tests.
Doctors track:
-
fatigue
-
appetite
-
dizziness
-
illness triggers
-
salt cravings
-
mental state
-
recovery after small dose increases
⭐ 7. How tapering decisions are made
Tapering depends on:
-
how long steroids have been taken
-
current dose
-
symptoms
-
test results
-
presence of illness
-
rate at which symptoms develop
-
allergy restrictions (pred/hydrocortisone allergy requires specialist handling)
General principles (not schedules):
-
Higher doses can reduce more quickly.
-
Taper slows dramatically near physiological levels
(~4–6 mg pred-equivalent). -
If symptoms appear → pause, slightly increase, or slow taper.
-
SST is used near the end to confirm recovery.
⭐ 8. When to contact your medical team
Same day advice needed
-
worsening dizziness
-
persistent nausea
-
new vomiting
-
symptoms appear with each taper step
-
fainting
-
new severe fatigue
-
any infection (urinary, chest, flu)
Urgent / A&E
-
collapse
-
severe vomiting/diarrhoea
-
confusion
-
severe abdominal pain
-
unable to take oral steroids
-
suspected adrenal crisis
⭐ 9. What patients should do to stay safe
-
Carry a Steroid Emergency Card at all times
-
Keep emergency instructions from your endocrinologist
-
Know your Sick Day Rules
-
Ensure A&E or ambulance crews know about corticosteroid allergy
-
Keep a written record of tapering plan
-
Never stop steroids suddenly
-
Be cautious during illness
-
Know your emergency steroid plan (alternative if allergic to hydrocortisone)
⭐ Final reassurance
Adrenal insufficiency during tapering is common, manageable, and often reversible.
By monitoring symptoms, using regular blood tests, and following specialist guidance, tapering can be done safely.
You are not alone — your endocrine team will guide every step, especially if allergies (to prednisolone or hydrocortisone) make your case more complex.
With careful observation and a clear emergency plan, serious complications are rare and preventable.
❤️ Thinking About Donating Blood After Aspergillosis or Lung Treatment?
A supportive message for people living with ABPA, CPA, SAFS, and related lung conditions
When you live with aspergillosis or a long-term lung condition, you know what it means to go through difficult treatments, long recoveries, and moments of uncertainty.
So when someone says, “Once I’m well, I’d like to donate blood to help others,” it is an incredibly generous and hopeful act.
Many people in our community wonder whether blood donation is possible after lung surgery, long-term inhalers, antifungals, or biologics. The reassuring answer is:
👉 Yes — some aspergillosis patients can donate blood once fully recovered, but it depends on individual treatments and health status.
And even if you can’t donate, the spirit behind the idea is powerful and meaningful.
🌱 1. Recovery comes first — your health is the priority
Whether you’ve had:
-
ABPA flare-ups
-
CPA treatment
-
bronchoscopy
-
long-term antifungals
-
biologics
-
a lobectomy or wedge resection
…the NHS will want you to be:
-
fully healed
-
breathing comfortably
-
stable in your lung condition
-
free from infection
-
strong enough to safely donate
For major surgery like a lobectomy, this often means several months of recovery before you can even be reviewed for donation.
This protects your health, not just the receiver’s.
💊 2. Medications commonly used for aspergillosis can affect eligibility
NHS Blood and Transplant will look closely at what you’re taking.
Here’s a simple guide:
Often NOT permitted
-
Biologics (e.g., mepolizumab, benralizumab, dupilumab)
-
Long-term immunosuppressants
-
Regular systemic steroids
May require a delay after stopping
-
Itraconazole / voriconazole / posaconazole
-
Recent antibiotic courses
-
Short steroid bursts
Usually fine
-
Inhalers
-
Nebulised saline
-
Montelukast
-
Airway clearance treatments
-
Most pain medicines
Every case is assessed individually — there is no automatic “yes” or “no” for all aspergillosis patients.
🫁 3. Your lung condition does not automatically exclude you
Having ABPA, CPA, bronchiectasis, or SAFS does not automatically prevent blood donation.
What matters is:
-
your condition is stable
-
your oxygen levels are good
-
you are not prone to sudden flare-ups
-
you feel well and strong
Many people with asthma or mild-to-moderate bronchiectasis still donate safely.
🩸 4. Your blood type is always valuable
Whether you’re a universal donor type (O-negative) or any other type, your blood can help save lives.
Even wanting to donate is something to be proud of — especially after everything you’ve been through.
🌟 5. The intention to donate speaks volumes about your strength
People living with aspergillosis know:
-
what it means to struggle for breath
-
how it feels to wait for test results
-
the exhaustion of flare-ups
-
the courage needed for surgery
-
the patience required for long-term treatment
So when someone in this community says:
“If I recover well, I want to donate blood to help someone else.”
…it’s a truly inspiring message of recovery and generosity.
🌈 6. Even if you can’t donate — your kindness still matters
Because of medications or long-term conditions, some people with aspergillosis will be told they can’t donate blood. This is completely normal.
You can still help others by:
-
encouraging friends or family to donate
-
sharing your story to raise awareness
-
supporting patient groups, campaigns, and research
-
simply being there for someone newly diagnosed
Your contribution to the world is not measured by a needle — it’s measured by your compassion.
❤️ Takeaway message
If you want to donate blood after aspergillosis treatment or lung surgery, that’s a beautiful intention. When you’re fully recovered, the NHS can review your health and medications. Whether you can donate or not, the willingness to help others already makes a real difference.
Why Join the Aspergillosis Patient Advisory Group (PAG)?
Supported by the European Lung Foundation (ELF), NAC CARES, and the European Respiratory Society (ERS).
Living with aspergillosis — CPA, ABPA, SAFS, Aspergillus bronchitis or sinus disease — can be overwhelming. Many people feel isolated, struggle to find clear information, or feel unsure how to influence the care they receive.
That is exactly why the Aspergillosis Patient Advisory Group (PAG) exists.
The PAG is supported by the European Lung Foundation (ELF) — based in Sheffield — and by NAC CARES, the patient engagement and support team at the UK National Aspergillosis Centre (NAC) in Manchester. Together, ELF, NAC CARES and the PAG work closely with the European Respiratory Society (ERS) to make sure the patient voice shapes research, education, and clinical practice across Europe and the UK.
What ELF Does
ELF brings together patients, carers, researchers and professionals from across Europe including the UK. It:
-
Provides clear, trustworthy patient information
-
Organises and hosts patient advisory groups
-
Ensures patient voices are included in ERS guidelines and research
-
Supports patient–professional workshops, surveys and consultations
-
Helps patients shape respiratory policy and awareness campaigns
Because ELF is UK-based, participation is easy for UK patients.
What NAC CARES Does
NAC CARES is the patient-facing team at the National Aspergillosis Centre in Manchester.
They:
-
Support UK patients to join the PAG
-
Help connect lived experience from UK clinics to the wider European PAG
-
Share updates, resources, and educational material
-
Bring PAG priorities back into NAC’s clinical and research work
-
Ensure UK patients feel included, represented and supported within ELF and ERS structures
NAC CARES acts as a bridge between UK clinical expertise and European patient involvement.
What the Aspergillosis PAG Does
The PAG ensures that people living with aspergillosis have a direct say in:
-
Research design
-
European Respiratory Society guidelines
-
New diagnostic and treatment pathways
-
Patient-friendly information materials
-
Awareness projects and health campaigns
-
Surveys that drive change in policy and clinical practice
Your lived experience is treated as meaningful expertise.
Why Join the PAG? Why Spend Your Energy?
Many people with aspergillosis have limited energy.
Here is why members say it is worth it:
1. You receive clear, reliable information
Updates on research, antifungals, biologics, trials and guidelines — written for patients, not scientists.
2. Your voice shapes real decisions
ERS guideline committees and research teams listen.
Your input changes how care is delivered.
3. You feel less alone
Aspergillosis is rare.
The PAG connects you with people across Europe and the UK who truly understand.
4. You choose how involved you want to be
You can simply receive updates — or you can complete the occasional survey, join a focus group, or help shape a guideline.
No pressure, no obligation.
5. It improves care for everyone — including you
Your experience helps highlight what really matters:
-
Delayed diagnosis
-
Side-effects
-
Treatment access
-
Fatigue and breathlessness
-
Impact on quality of life
This evidence influences clinicians, researchers and policymakers.
6. It is free, inclusive and easy to join
No travel.
No cost.
All online.
Europe includes the UK, and ELF is based in Sheffield.
Who Can Join?
Anyone affected by aspergillosis:
-
Patients with CPA, ABPA, SAFS, Aspergillus bronchitis or sinus disease
-
People with fungal allergy in asthma or bronchiectasis
-
Family members and carers
No medical background needed.
How to Join
You can join in a few minutes:
👉 https://europeanlung.org/en/patient-advisory-groups/
Choose “Aspergillosis”.
You’ll then receive updates and invitations to take part — always at your own pace.
In One Line:
The PAG gives you good information, a real voice in shaping aspergillosis care, and a supportive community — with full backing from ELF, ERS and NAC CARES.
🌿 Why We All Need to Advocate for Ourselves as the NHS Faces Change and Pressure
A patient-friendly guide to staying safe and getting the care you need
The NHS is going through one of the most challenging periods in its history. Services are under pressure, staff are stretched, and backlogs remain high across nearly every speciality. None of this is the fault of patients or staff — it’s the reality of a system trying to do too much with too little.
In times like this, one thing becomes more important than ever:
⭐ Advocating for your own health.
Advocacy simply means speaking up when you need help, asking questions, and making sure your concerns are heard. It’s not about complaining or demanding; it’s about ensuring you get the support, information, and care you deserve.
Here’s why it matters — and how to do it safely and confidently.
🔍 1. Some things no longer happen automatically
With so many clinics running over capacity, routine tasks can be delayed or missed:
-
Follow-up appointments don’t always get booked
-
Test results aren’t always communicated quickly
-
Reviews may slip off the system
-
New medications sometimes aren’t monitored as closely as they should be
This isn’t because your team doesn’t care.
It’s because the system is stretched.
Advocating for yourself helps fill the gaps.
💬 2. Asking questions keeps you safer
If something is unclear — a result, a new medication, a change in symptoms, or a delay — asking for clarification is not only reasonable, it’s sensible.
Good questions to ask:
-
“When should my next review be?”
-
“Who do I contact if I have a problem?”
-
“What symptoms should I watch for?”
-
“Is there a plan for monitoring?”
Healthcare teams want patients to feel informed.
They would rather you ask than worry in silence.
📞 3. The NHS wants patients to raise concerns early
Early contact helps prevent:
-
deteriorations
-
emergency admissions
-
medication complications
-
worsening long-term conditions
Services rely on patients saying, “Something isn’t right.”
It’s an essential part of safe care, not an inconvenience.
🧭 4. The NHS is changing — and patients play a role in shaping care
Integrated Care Systems (ICS), value-based care, and new digital pathways are all evolving.
These changes aim to make care:
-
more personalised
-
more consistent
-
more focused on real outcomes
But during transitions, there are bumps in the road.
Patient feedback — including when something hasn’t worked — helps services identify where improvements are needed.
You are part of shaping that improvement.
❤️ 5. You deserve to be heard
Many patients worry about “bothering” the NHS.
But advocating for yourself is:
-
responsible
-
appropriate
-
encouraged
-
part of keeping long-term conditions well-managed
You are not asking for anything unreasonable.
You are simply making sure your health is looked after.
🌼 6. How to advocate confidently
Here are gentle, effective ways to speak up:
Be clear
“I haven’t had a review since starting this treatment — can we arrange one?”
Be specific
“I’m unsure who to contact if I worsen. Could you give me the correct number?”
Be persistent if needed
“It’s been a few weeks since I asked — could you update me on the appointment?”
Keep records
Dates, names, symptoms, and messages help everything run more smoothly.
Ask for your named clinician or team
Every patient is entitled to know who oversees their care.
🌟 7. You are not alone — and it’s OK to ask for help
Advocacy doesn’t mean you carry the burden alone.
Groups like NAC, patient communities, and charities can help you:
-
understand the system
-
find the right contacts
-
prepare questions
-
know what to expect
-
get support if you’re struggling to be heard
Empowering yourself helps others too — the more patients speak up, the more the system adapts.
💚 In summary
The NHS is still full of dedicated people who care deeply about their patients.
But the reality of high demand and limited capacity means:
We all have to be a little more active in asking for what we need.
Advocating for your own health is:
-
responsible
-
protective
-
empowering
-
part of modern healthcare
It ensures you get the right care at the right time — and it helps the NHS deliver safer, more responsive services.









