2003
DOI: 10.1038/sj.leu.2402921
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Diffuse alveolar hemorrhage: an evolving problem?

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Cited by 16 publications
(12 citation statements)
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“…In general, emergent medical therapy is the first treatment option in hematologic patients with coagulopathy and diffuse alveolar hemorrhage (18). However, in our results, there was no statistically significant difference in clinical success rate and survival rate between patients with coagulopathy or diffuse alveolar hemorrhagic pattern and other hematologic patients.…”
Section: Discussioncontrasting
confidence: 54%
See 1 more Smart Citation
“…In general, emergent medical therapy is the first treatment option in hematologic patients with coagulopathy and diffuse alveolar hemorrhage (18). However, in our results, there was no statistically significant difference in clinical success rate and survival rate between patients with coagulopathy or diffuse alveolar hemorrhagic pattern and other hematologic patients.…”
Section: Discussioncontrasting
confidence: 54%
“…In general, diffuse alveolar hemorrhage is a hemorrhagic syndrome, but it is not associated with hemoptysis because the alveolar epithelium is not just leaking fluid but is perforated sufficiently to leak red cells (18). Thus, aggressive correction of thrombocytopenia and coagulation disturbances may be the first and sufficient treatment option (18). Massive pulmonary hemorrhage that can induce hemoptysis is an uncommon complication of leukemia and is generally attributed to thrombocytopenia.…”
Section: Discussionmentioning
confidence: 99%
“…[1][2][3][4]12 Notwithstanding the limitation of small sample size, we observed no benefit with high-dose corticosteroids in hemorrhage occurring after RIC allogeneic HCT. Although all patients with DAH and the majority of patients with IAH in our RIC cohort received high-dose methylprednisolone, 60-day survival from hemorrhage onset was only 28%.…”
Section: Discussionmentioning
confidence: 61%
“…Infections, cardiac causes including heart failure, toxicity from pretransplant thoracic radiation, chemotherapy, early marrow engraftment, GVHD and cytokines have been postulated to have a role in the pathogenesis of AH after HSCT. [11][12][13][14][15][16][17][18] The reported mortality associated with AH varies from 70 to 100%. [11][12][13][14] Diffuse AH (DAH) was initially described in autologous HSCT recipients and since has been described with equal frequency in both allogeneic and autologous transplant recipients.…”
Section: Introductionmentioning
confidence: 99%