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PedAM

Pediatric Disease Annotations & Medicines




Disease pulmonary hypertension
Phenotype C1145670|respiratory failure
Sentences 17
PubMedID- 22295020 Inhaled no (ino) is a selective pulmonary vasodilator and is used in severe hypoxaemic respiratory failure associated with pulmonary hypertension.
PubMedID- 22170702 Objective: to describe a series of ex-preterm infants admitted to pediatric intensive care unit due to impending hypoxaemic respiratory failure complicated by pulmonary hypertension (ph) who were treated electively combining noninvasive ventilation (niv) and nebulized iloprost (nebilo).
PubMedID- 25615715 Background: among neonates with down syndrome (ds) and transient leukemia (tl), hyperleukocytosis (white blood cell [wbc] count >100 x 10(9) /l) is associated with increased blood viscosity, respiratory failure due to pulmonary hypertension, multiorgan failure, and increased risk of early death.
PubMedID- PMC4033916 There were three deaths due to respiratory failure with severe pulmonary hypertension.during follow-up, two children required additional right heart procedures and one developed a non-compaction cardiomyopathy [11].
PubMedID- 21869934 Such targeted controlled release of no could be an effective therapy for hypoxic respiratory failure associated with pulmonary hypertension.
PubMedID- 21378553 This question is clinically relevant in respiratory failure associated with pulmonary hypertension, in particular in newborn infants with persistent pulmonary hypertension.
PubMedID- 22837854 Inhaled nitric oxide (ino) is approved for the treatment of hypoxic respiratory failure associated with pulmonary hypertension in term/near-term neonates.
PubMedID- 25298767 In cases of rapidly progressing respiratory failure with pulmonary hypertension, it is necessary to consider pttm in the differential diagnosis.
PubMedID- 21465122 The clinical picture varies from mild tachypnoea to life-threatening respiratory failure associated with pulmonary hypertension [16].
PubMedID- 25360412 A young woman with terminal respiratory failure due to idiopathic pulmonary hypertension underwent bilateral lung transplantation.
PubMedID- 22720178 Similar to our infant, the postnatal clinical course of mpc is usually characterised by cardiorespiratory failure due to pulmonary hypertension, prolonged abdominal distension [6, 7].
PubMedID- 25887097 The disease can resolve spontaneously, remain stable, or progress to respiratory failure with severe pulmonary hypertension (ph), requiring lung transplantation [1,2,4].
PubMedID- 26484320 Both siblings near 35 hours of age presented severe respiratory failure due to pulmonary hypertension.
PubMedID- 20921917 Patient: an 8-wk-old girl was diagnosed with malignant pertussis (extreme leukocytosis, seizures, pneumonia, and secondary severe hypoxic respiratory failure associated with pulmonary hypertension).
PubMedID- 22655195 Persistence of pulmonary hypertension leading to respiratory failure in the neonate has been recognized for 40 years since its original description by gersony and colleagues in 1969 [6].
PubMedID- 23343739 Within a few days, each developed rapidly progressive respiratory failure complicated by refractory pulmonary hypertension due to malignant pertussis.
PubMedID- 26346417 After a stabilization period of 6years, the patient gradually developed chronic respiratory failure with moderate pulmonary hypertension requiring long-term oxygen therapy and nocturnal non-invasive ventilation.

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