Nis · Clinic

Department — Chest & Respiratory Medicine

Chest & Respiratory Medicine

Asthma, COPD, pneumonia, sleep apnoea, and lung cancer screening — all under one roof.

The Nis Clinic Pulmonology department provides diagnosis, treatment, and long-term follow-up of lung and airway conditions. The department covers the full spectrum of respiratory medicine, including chronic obstructive conditions such as asthma and COPD, pneumonia and acute respiratory infections, lung cancer screening, and sleep apnoea. Spirometry and lung function tests are performed in-house; patients requiring advanced imaging (thoracic CT, low-dose CT screening) or polysomnography are referred to partner facilities. The department's lead physician appointment is currently in progress; in the interim, all content is published under Nis Clinic editorial review.

What Is Pulmonology and When Should You Seek Care?

Pulmonology is the internal medicine specialty concerned with diseases of the lungs, pleura, mediastinum, and airways. Surgical chest conditions (thoracic surgery) constitute a separate field; pulmonology manages the medical side and refers to surgery when indicated.

The most common reasons patients visit our department:

  • Cough lasting more than two weeks — dry or productive
  • Shortness of breath — on exertion or at rest
  • Wheezing or chest tightness — particularly at night or in the early morning
  • Recurrent upper or lower respiratory tract infections
  • Lung cancer screening requests in adults with a smoking history
  • Night-time snoring, excessive daytime sleepiness, witnessed apnoea
  • Coughing up blood (haemoptysis) — requires urgent assessment
  • Lung monitoring following occupational exposure (dust, chemicals, asbestos)

Respiratory symptoms frequently overlap with presentations from other specialties — cardiology, ENT, and allergy. Distinguishing a cardiac cause of breathlessness from an upper airway cause of wheeze is critical for early diagnosis; for this reason our department conducts joint assessments with cardiology and ENT when clinically indicated.

Asthma and Allergic Respiratory Conditions

Asthma is a condition characterised by chronic airway inflammation and variable airflow obstruction. Distinguishing between acute episodes and the interval period shapes the treatment plan.

Diagnostic assessment includes:

  • Clinical history (attack pattern, triggers, family history)
  • Spirometry (FEV1, FEV1/FVC) and bronchodilator reversibility testing
  • Peak expiratory flow (PEF) monitoring — particularly relevant in occupational asthma
  • Allergy history and referral for allergy testing where appropriate
  • Comorbidity screening (rhinitis, GORD, obesity)

Principles of acute episode management:

A mild-to-moderate episode can often be managed at home with a short-acting bronchodilator (SABA) and, if necessary, oral corticosteroids. A severe episode requires hospital attendance. Cyanosis, breathlessness severe enough to prevent speech, oxygen saturation below 92%, and tachycardia are criteria for emergency referral. Our recommendation: every patient with asthma should have a written action plan setting out when to increase medication and when to go to A&E — documented in advance.

Inhaler technique: More than 50% of asthma treatment success depends on correct inhaler technique. We review inhaler technique at every outpatient appointment; many patients fail to benefit adequately from treatment simply because they have used their inhaler incorrectly for years. A spacer device is our standard recommendation for children and adults with hand tremor.

Allergic component: Seasonal triggers (pollen), house dust mite, pets, mould, cold air, and exercise all provoke asthma episodes. Identifying triggers is as valuable as medication itself. Indoor modifications — mattress covers, humidity control, rules around pet contact — are part of the treatment plan.

COPD: Diagnosis, Staging, and Follow-Up

Chronic Obstructive Pulmonary Disease (COPD) is a condition caused by prolonged exposure to tobacco smoke and other harmful particles, characterised by irreversible airflow limitation. Its key distinction from asthma: the FEV1/FVC ratio remains persistently reduced after bronchodilator administration.

Diagnostic framework:

  • Smoking history: Pack-year calculation (packs per day × years smoked). A history of 20+ pack-years represents a significant risk threshold.
  • Spirometry: Post-bronchodilator FEV1/FVC < 0.70 is consistent with COPD. Staging is based on FEV1 percentage (GOLD grades 1–4).
  • Symptom scoring: CAT (COPD Assessment Test) or mMRC dyspnoea scale. Symptom burden can vary considerably between patients sharing the same FEV1 value.
  • Exacerbation history: Number of deteriorations and hospitalisations in the past 12 months.
  • Comorbidities: Cardiovascular disease, osteoporosis, depression, and muscle-mass loss are closely associated with COPD.

Stepwise pharmacological therapy:

Treatment is stratified according to symptom burden and exacerbation risk, in line with GOLD guidelines:

  • Long-acting bronchodilator (LAMA or LABA) monotherapy — for low-risk symptomatic patients
  • LABA + LAMA combination — when symptom control is inadequate
  • Triple therapy (LABA + LAMA + ICS) — for patients with high exacerbation burden and eosinophilia

Inhaler technique capability, comorbidities, and cost are all considered when selecting treatment.

Oxygen therapy: In patients with a resting arterial oxygen tension (PaO2) persistently below 55 mmHg, or oxygen saturation consistently below 88%, long-term oxygen therapy (LTOT) is the only intervention proven to extend survival. Eligibility is assessed via arterial blood gas analysis; oxygen is initiated on the basis of confirmed clinical indication, not for symptomatic comfort.

Smoking cessation: The single most effective intervention to slow disease progression in COPD is stopping smoking. No medication produces a comparable effect. Smoking status is addressed at every consultation without exception.

Pneumonia and Acute Respiratory Tract Infections

Pneumonia is an infectious inflammation of the lung parenchyma. The distinction between community-acquired pneumonia (developing outside hospital) and hospital-acquired pneumonia directly determines treatment choice.

Community-acquired pneumonia — clinical approach:

  • Fever, cough, sputum, pleuritic chest pain, shortness of breath
  • In older patients, the classic presentation may be replaced by confusion, general malaise, and loss of appetite
  • A chest X-ray supports the diagnosis; clinical suspicion is not excluded by a negative film
  • Identifying a causative organism is not always necessary; empirical treatment is sufficient in most cases

Treatment decisions are guided by the following questions:

  1. Can the patient be treated at home, or is hospital admission required?
  2. What is the patient's age, comorbidity profile, and recent antibiotic history?
  3. What are the current local resistance patterns?

Hospital referral criteria (CURB-65 score):

  • Confusion
  • Urea > 7 mmol/L (BUN > 19 mg/dL)
  • Respiratory rate ≥ 30/min
  • Blood pressure (systolic < 90 or diastolic ≤ 60)
  • 65 years of age or over

Each criterion scores 1 point. A score of 0–1 supports home treatment; 2 suggests close monitoring or admission; 3 or more warrants hospital admission. This scoring tool is not a mechanical rule — it must be interpreted alongside the full clinical picture.

High-risk groups: Pneumonia follows a more severe course in adults aged over 65, those with underlying COPD or heart failure, and immunocompromised patients. Pneumococcal and influenza vaccines are our standard recommendation for these groups; vaccination status is reviewed at every autumn appointment.

Recovery: Patients treated at home can expect symptoms to begin improving within 48–72 hours. If fever persists, breathlessness worsens, or the patient is unable to maintain adequate fluid intake, the follow-up appointment is brought forward. Radiological resolution typically lags behind clinical improvement; a follow-up chest X-ray is requested when clinically indicated, not routinely.

Lung Cancer Screening and Early Detection

Lung cancer is most often diagnosed at a locally advanced or metastatic stage. Because five-year survival is significantly higher when caught at an early stage, screening programmes are critically important.

Low-dose thoracic CT (LDCT) screening — who is eligible?

Internationally accepted screening criteria:

  • Age 50–80 years
  • A smoking history of 20 or more pack-years
  • Currently smoking, or having stopped within the past 15 years

Patients who meet all three criteria are candidates for annual low-dose CT screening. Routine CT screening is not recommended for those who do not meet these criteria; the risks of unnecessary radiation exposure and false-positive findings outweigh the benefits.

Interpreting screening results:

  • Lung-RADS 1–2 (negative or benign): Continue annual screening
  • Lung-RADS 3 (probably benign): Follow-up CT in 6 months
  • Lung-RADS 4 (suspicious): Short-interval CT, PET-CT, or referral for biopsy

Not every nodule found on a screening CT is cancer; more than 95% of nodules are benign. Our role is to accurately filter which nodules warrant further investigation.

Biopsy referral: The biopsy method for a suspicious nodule depends on its location. Central lesions are approached via bronchoscopy; peripheral lesions via CT-guided transthoracic needle biopsy; mediastinal lymph node involvement via EBUS (endobronchial ultrasound-guided biopsy). Referral to a specialist centre is arranged for these procedures.

Approach to patients who smoke: A screening CT is an opportunity to motivate smoking cessation. A "clear CT" result should not reassure the patient into complacency — it should be framed as "a reason to stop". Smoking status is reviewed at every visit; smoking cessation support programmes, nicotine replacement therapy, and pharmacotherapy where appropriate (varenicline, bupropion) are offered.

Sleep Apnoea and CPAP Therapy

Obstructive sleep apnoea syndrome (OSAS) is characterised by repeated upper airway collapse during sleep, causing oxygen desaturation and disrupted sleep architecture. It is a common condition that remains largely undiagnosed.

Signs that raise clinical suspicion:

  • Loud, irregular snoring at night
  • Witnessed apnoea — breathing pauses observed by a bed partner
  • Excessive daytime sleepiness, difficulty concentrating, waking unrefreshed
  • Morning headache, frequent nocturnal urination
  • Treatment-resistant hypertension
  • Large neck circumference, obesity

Polysomnography (sleep study): The gold standard for diagnosis. The patient is monitored overnight in a sleep laboratory with electrodes attached; the apnoea–hypopnoea index (AHI) is calculated.

  • AHI 5–15: mild OSAS
  • AHI 15–30: moderate OSAS
  • AHI > 30: severe OSAS

Our department does not have an in-house polysomnography facility; patients are referred to a partner sleep laboratory and we review the report together.

CPAP therapy: The first-line treatment for moderate-to-severe OSAS. Continuous Positive Airway Pressure keeps the upper airway open during sleep, preventing apnoeic episodes and oxygen desaturation. Pressure titration is tailored to the individual patient.

CPAP adherence is the most critical factor: Treatment success depends directly on consistent device use. The first one to three months are an adaptation period — mask discomfort, dry mouth, and a sense of claustrophobia are common complaints. At follow-up appointments, adherence data (hours of use, leak rate, residual AHI) is downloaded from the device memory; if problems are identified, mask type, pressure settings, or humidifier settings are adjusted accordingly.

Alternative treatments: For mild OSAS, anatomically correctable causes, or patients who cannot tolerate CPAP, options include a mandibular advancement device (oral appliance), a weight loss programme, positional therapy (supine avoidance), and — in selected anatomical cases — ENT referral for upper airway surgery. Where upper airway obstruction is suspected, joint assessment with the Nis Clinic ENT department is arranged.

Frequently Asked Questions

When should a persistent cough prompt a visit to the doctor?
A cough lasting more than three weeks falls into the subacute or chronic category and warrants assessment. A cough persisting beyond eight weeks meets the definition of chronic cough; the most common causes are post-nasal drip, asthma, and gastro-oesophageal reflux, but in patients with a smoking history, lung cancer must be included in the differential diagnosis. Situations requiring urgent assessment: blood in sputum, weight loss accompanied by night sweats, progressively worsening breathlessness, hoarseness lasting more than three weeks.
How long does it take for the lungs to recover after stopping smoking?
The benefits of stopping smoking are measurable from the first few weeks. Within 48 hours, carbon monoxide levels return to normal and the senses of smell and taste sharpen. Within 2–3 weeks, circulation improves and coughing temporarily increases as ciliary function is restored. Within 1–9 months, cough and breathlessness diminish and resistance to respiratory infections improves. After 1 year, the risk of coronary heart disease falls to half that of a current smoker. After 10–15 years, the risk of lung cancer approaches that of a lifelong non-smoker. In COPD, structural damage cannot be reversed, but the rate of disease progression slows — and that is the most important gain.
What should I do at home during an asthma attack?
If you have a written asthma action plan, follow it. If not, the general approach is: use your short-acting bronchodilator (blue reliever inhaler — salbutamol) 2–4 puffs every 15–20 minutes, using a spacer device if available. Remain seated upright and try to stay calm. Criteria for calling emergency services or attending A&E: breathlessness too severe to speak, blue discolouration of the lips, reliever inhaler lasting less than one hour, peak flow falling below 50% of your personal best, or a markedly elevated heart rate. An asthma attack can be life-threatening — if in doubt, seek emergency care without delay.
What tests are needed to diagnose COPD?
Spirometry (lung function testing) is essential for diagnosis. A post-bronchodilator FEV1/FVC below 0.70 is consistent with COPD. Alongside spirometry, the assessment includes clinical history (smoking/pack-year history, occupational exposures), physical examination, chest X-ray, and thoracic CT where indicated. Arterial blood gas analysis is used in advanced-stage disease or when assessing eligibility for oxygen therapy; alpha-1 antitrypsin levels should be considered in patients under 45 years of age or in non-smokers with COPD. Spirometry alone is not sufficient — it must be interpreted in the context of the full clinical picture.
What is spirometry and how is it performed?
Spirometry is a non-invasive test that measures lung capacity and airflow velocity. You breathe in deeply through a mouthpiece, then exhale as forcefully and for as long as possible. The test takes 15–20 minutes; at least three attempts are made and the best result is recorded. If post-bronchodilator testing is requested, the measurement is repeated 15 minutes after inhaler administration (bronchodilator reversibility test). Before the test, you will be asked to avoid short-acting bronchodilators for 4–6 hours, long-acting bronchodilators for 12 hours, and once-daily medications such as tiotropium for 24 hours. Written instructions specifying which medicines to withhold and when will be provided at your pre-appointment check-in.
Am I a candidate for lung cancer screening?
Individuals aged 50–80 years with a smoking history of 20 or more pack-years who currently smoke or stopped within the past 15 years are candidates for low-dose thoracic CT screening. Pack-year calculation: number of packs smoked per day × number of years. For example, one pack per day for 25 years equals 25 pack-years. Routine screening is not recommended for non-smokers or those who do not meet the criteria — the risk of unnecessary radiation exposure and false-positive findings outweighs the benefit. If additional risk factors are present, such as a family history of lung cancer or occupational exposure (asbestos, radon), individual assessment is arranged.
I snore — could I have sleep apnoea?
Not all snoring indicates sleep apnoea; however, the combination of loud, irregular snoring + witnessed apnoea + excessive daytime sleepiness raises significant clinical suspicion. Risk factors include obesity, large neck circumference (above 43 cm in men or 38 cm in women), age over 50, receding jaw structure, and treatment-resistant hypertension. Where there is clinical suspicion, polysomnography (a sleep study) is required to confirm the diagnosis. In patients diagnosed with moderate-to-severe OSAS, CPAP therapy extends survival, reduces cardiovascular risk, and produces a marked improvement in quality of life.
My child keeps getting bronchitis — could it be asthma?
Recurrent episodes of wheeze and cough in a child raise a strong possibility of asthma. Features that particularly suggest asthma include night-time cough, exercise-induced wheeze, a history of allergic conditions (eczema, allergic rhinitis, food allergy), or a family history of asthma. Diagnosis in children differs from adults — spirometry may not be feasible in young children and clinical history combined with treatment response becomes the determining factor. If your child shows this pattern, referral to a paediatrician or paediatric respiratory specialist is the appropriate first step. Our adult pulmonology clinic covers patients aged 18 and over.

Editorial Review

Nis ClinicClinical Content Editor — Lead physician appointment pending

Clinical Content Editor — Lead physician appointment pending

Last reviewed:

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