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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