2000
DOI: 10.1002/1099-0496(200011)30:5<393::aid-ppul5>3.0.co;2-w
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Pulmonary complications after bone marrow transplantation in children: Twenty-four years of experience in a single pediatric center

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Cited by 126 publications
(51 citation statements)
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“…However, viral infections, encapsulated bacteria, and P jiroveci, in particular, can occur months later. 25 Noninfectious pulmonary complications include diffuse alveolar hemorrhage (DAH), idiopathic pneumonia syndrome (IPS), bronchiolitis obliterans (BO), and BO with organizing pneumonia (BOOP), a manifestation of cGVHD. 26-29 Table 3 describes the presenting symptoms and diagnostic features of noninfectious pulmonary complications after HCT.…”
Section: Discussion Casementioning
confidence: 99%
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“…However, viral infections, encapsulated bacteria, and P jiroveci, in particular, can occur months later. 25 Noninfectious pulmonary complications include diffuse alveolar hemorrhage (DAH), idiopathic pneumonia syndrome (IPS), bronchiolitis obliterans (BO), and BO with organizing pneumonia (BOOP), a manifestation of cGVHD. 26-29 Table 3 describes the presenting symptoms and diagnostic features of noninfectious pulmonary complications after HCT.…”
Section: Discussion Casementioning
confidence: 99%
“…25,27,28,33 Small retrospective studies have shown that the incidence of LONIPCs is 10% to 15% in pediatric patients who have undergone HCT. 25,27,33 Patients at the greatest risk of developing these complications are those who have undergone allogeneic HCT or have severe cGVHD. Bronchiolitis obliterans, especially, is thought to be a form of cGVHD of the lungs and may be seen with other manifestations of cGVHD.…”
Section: Discussion Casementioning
confidence: 99%
See 1 more Smart Citation
“…Pulmonary complications develop in 25-60% of HSCT recipients and account for approximately 50% of transplant-related deaths. [1][2][3] Pulmonary complications after HSCT include infectious or noninfectious causes, defined as early or late, according to the time of onset after transplant. Idiopathic pneumonia syndrome describes a clinical entity of diffuse lung injury that occurs around 90 days post-transplant and for which no infectious cause can be identified.…”
Section: Introductionmentioning
confidence: 99%
“…The P aO 2 /F IO 2 was 209 mm Hg and the Murray score was 1.5 on ICU day 10. On ICU day 18, despite an increase in peak inspiratory pressure (PIP) up to 26 cm H 2 O, the worsening hypercapnia was persistent (pH 7.233, P aCO 2 71.5 mm Hg, HCO 3 Ϫ 29.5 mmol/L, P aO 2 /F IO 2 131 mm Hg), with a Murray score of 3. The ventilator mode was pressure regulated volume control, tidal volume was 6.2 mL/ kg, PEEP was 14 cm H 2 O, and F IO 2 was 0.8.…”
Section: Introductionmentioning
confidence: 99%