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DR ASHRAF AHMAD
PULMONOLOGIST
KAASH - TAIF
2015
DIFFUSE ALVEOLAR HAEMORRHAGE
INTRODUCTION
Bleeding into the alveolar spaces characterizes the
syndrome of DAH and is due to disruption of the
alveolar-capillary basement membrane. This is
caused by injury or inflammation of the
arterioles, venules, or alveolar septal (alveolar
wall or interstitial) capillaries. Hemoptysis is the
usual presenting symptom; however it is not
always present, even when hemorrhage is severe
CLINICAL PRESENTATION
 Symptoms :Cough, hemoptysis, fever, and dyspnea
are common initial symptoms. Some patients,
however, present with ARDS requiringMV
 Physical examination: The pulmonary examination
is usually nonspecific, unless there are physical
signs of an underlying systemic vasculitis or CT
vascular disorder
INVESTIGATIONS
 Radiological:
 PFTs: increased DLCO
 BAL :sequential lavage are progressively more
hemorrhagic with hemosiderin-ladenMQ.
 Biopsy from the affected tissue
TREATMENT
=TTT CAUSE
 Glucocorticoids : are the mainstay of therapy for
the DAH syndrome associated with systemic
vasculitis, connective tissue disease, Goodpasture's
syndrome, and isolated pulmonary capillaritis.
 Additional immunosuppressive
agents (cyclophosphamide or azathioprine)
 Plasma exchange : in Goodpasture's syndrom
 Experimental TTT:
IVIG, rituximab , aminocaproic acid &
Recombinant human coagulation factor VIIa

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DIFFUSE ALVEOLAR HAEMORRHAGE

  • 1. DR ASHRAF AHMAD PULMONOLOGIST KAASH - TAIF 2015 DIFFUSE ALVEOLAR HAEMORRHAGE
  • 2. INTRODUCTION Bleeding into the alveolar spaces characterizes the syndrome of DAH and is due to disruption of the alveolar-capillary basement membrane. This is caused by injury or inflammation of the arterioles, venules, or alveolar septal (alveolar wall or interstitial) capillaries. Hemoptysis is the usual presenting symptom; however it is not always present, even when hemorrhage is severe
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  • 7. CLINICAL PRESENTATION  Symptoms :Cough, hemoptysis, fever, and dyspnea are common initial symptoms. Some patients, however, present with ARDS requiringMV  Physical examination: The pulmonary examination is usually nonspecific, unless there are physical signs of an underlying systemic vasculitis or CT vascular disorder
  • 8. INVESTIGATIONS  Radiological:  PFTs: increased DLCO  BAL :sequential lavage are progressively more hemorrhagic with hemosiderin-ladenMQ.  Biopsy from the affected tissue
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  • 12. TREATMENT =TTT CAUSE  Glucocorticoids : are the mainstay of therapy for the DAH syndrome associated with systemic vasculitis, connective tissue disease, Goodpasture's syndrome, and isolated pulmonary capillaritis.  Additional immunosuppressive agents (cyclophosphamide or azathioprine)  Plasma exchange : in Goodpasture's syndrom
  • 13.  Experimental TTT: IVIG, rituximab , aminocaproic acid & Recombinant human coagulation factor VIIa