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π‘ Key Point: Lung transplantation is life-saving for end-stage lung disease but carries high risks of infection, rejection, and long-term complications due to lifelong immunosuppression.
π About
- Procedure involves replacing one or both diseased lungs with donor lungs.
- Performed as single or double lung transplants depending on the underlying condition.
- Generally offered to patients <60 years, though exceptions exist.
- Requires lifelong immunosuppression (Ciclosporin, Tacrolimus, Steroids, Mycophenolate, Azathioprine, anti-lymphocyte globulin).
- Immunosuppression β π¨ high risk of opportunistic infections.
π« Types
- Single Lung Transplant: Used in conditions with infection risk confined to one lung (e.g. COPD, IPF).
- Double Lung Transplant: Both lungs replaced (sequentially). Preferred in Cystic Fibrosis, IPF, Pulmonary Hypertension.
π― Indications
- Cystic Fibrosis (β‘οΈ DOUBLE).
- Emphysema & Alpha-1 antitrypsin deficiency.
- Idiopathic Pulmonary Fibrosis.
- Advanced COPD.
- Connective tissueβrelated pulmonary fibrosis.
- Chronic Hypersensitivity Pneumonitis.
- Advanced Sarcoidosis.
- Primary Pulmonary Hypertension (β‘οΈ DOUBLE).
- Rare diseases: Langerhans cell granulomatosis, Lymphangioleiomyomatosis.
β οΈ Complications
- Infections: CMV, Aspergillus, PJP; risk highest if donor seropositive & recipient seronegative.
- Acute Rejection: Weeksβmonths; managed by β immunosuppression.
- Chronic Rejection: Bronchiolitis Obliterans Syndrome (BOS) β progressive breathlessness & airflow limitation.
- Drug Toxicity: Calcineurin inhibitors β nephrotoxicity & hypertension.
- Malignancy: Skin cancers & post-transplant lymphoproliferative disorder (PTLD).
- GI Side Effects: Nausea, diarrhoea, peptic ulcer disease.
π©Ί Post-Transplant Care
- π Monitor lung function (spirometry, imaging) for early rejection.
- π¬ Screen for infections (CMV, PJP, Aspergillus).
- π Prophylaxis: TMP-SMX (Bactrim) for PJP, antivirals if indicated.
- πββοΈ Pulmonary rehab for recovery & QoL.
- βοΈ Regular drug-level monitoring to balance efficacy vs toxicity.
- π’ Patient education: adherence, infection precautions, recognising rejection.
π Prognosis
- Median survival: 5β7 years, though some survive much longer.
- Better outcomes: Younger patients, double lung transplants, cystic fibrosis.
- Chronic rejection (BOS) β leading cause of late mortality.
- Careful monitoring improves QoL and prolongs survival.
π References
3 Clinical Cases β Lung Transplantation π«π
- Case 1 β End-stage COPD π¬: A 62-year-old man with GOLD stage 4 COPD, FEVβ 22% predicted, on long-term oxygen therapy, presents with worsening breathlessness despite maximal inhaler therapy and pulmonary rehab. Multiple admissions in past year. Teaching: COPD is the commonest indication for lung transplant worldwide. Candidates are selected when prognosis is poor and quality of life severely impaired despite optimal treatment. Typically offered a single lung transplant if age/fitness appropriate.
- Case 2 β Idiopathic Pulmonary Fibrosis π«οΈ: A 55-year-old woman with rapidly progressive IPF (FVC 38% predicted, DLCO 30%) is hypoxaemic at rest and desaturates with exertion. She is referred early for transplant assessment. Teaching: IPF carries the worst prognosis of the interstitial lung diseases. Double lung transplantation is usually performed, as single lung grafts are at higher risk of infection and poor long-term function.
- Case 3 β Cystic Fibrosis π§¬: A 28-year-old woman with CF and chronic Pseudomonas colonisation has severe bronchiectasis, FEVβ 18% predicted, and recurrent haemoptysis requiring embolisation. She is cachectic despite nutritional support. Teaching: Bilateral lung transplantation is the only curative option in advanced CF. It removes the diseased lungs and associated reservoir of infection. Post-op care requires aggressive immunosuppression and infection prophylaxis.