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The objective was to evaluate the effect of nebulized nitroglycerin (NNG) in neonates with persistent pulmonary hypertension (PPHN). The study focused on assessing changes in echocardiographic and clinical parameters following its administration. This is a randomized controlled trial that included 80 full-term newborns diagnosed with PPHN within 72 h after birth. Participants were randomized into two groups: the NNG group received nebulized nitroglycerin, while the control group did not receive it as adjunctive therapy to PPHN. Clinical parameters and echocardiographic measures were evaluated before intervention, and subsequently at 24 and 48 h. The primary outcome was the estimated systolic pulmonary artery pressure in both groups. Comparative analyses were conducted between the groups, along with repeated measures within each group. The NNG group exhibited a significant improvement in the oxygenation index and oxygen saturation index (OI&OSI) on days 2 and 3. There was a marked reduction in the systolic pulmonary artery pressure/systolic systemic pressure (SPAP/SSP) ratio, accompanied by a significant enhancement in biventricular systolic function and cardiac output. The myocardial performance index (MPI), as measured by tissue-Doppler echocardiography, was notably decreased in the NNG group on day 3. Furthermore, the requirements for ventilatory support and inotropic agents were significantly lower in the NNG group. Survival analysis indicated a more favorable weaning course in the NNG group.Conclusion: NNG was effective in managing neonates with PPHN and might be a promising, alternative therapy for PPHN, especially in settings where inhaled nitric oxide is unavailable.Trial registration: Clinical-Trial.gov identifier: NCT05741229 and was registered on February 14, 2023. URL: https://clinicaltrials.gov/study/NCT05741229 .
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http://dx.doi.org/10.1007/s00431-025-06381-5 | DOI Listing |
Eur J Pediatr
September 2025
Pediatric Department, Alexandria University Hospital, Alexandria, Egypt.
The objective was to evaluate the effect of nebulized nitroglycerin (NNG) in neonates with persistent pulmonary hypertension (PPHN). The study focused on assessing changes in echocardiographic and clinical parameters following its administration. This is a randomized controlled trial that included 80 full-term newborns diagnosed with PPHN within 72 h after birth.
View Article and Find Full Text PDFHaemophilia
July 2025
Keck School of Medicine of the University of Southern California, Los Angeles, California, USA.
Introduction: Accurate and reproducible measures of factor activity are required to guide clinical decision-making following gene therapy for haemophilia B (HB). Highly significant discrepancies have been observed in measurements of various factor IX (FIX) concentrates that carry molecular modifications to extend their half-life, arguing for the need for careful analysis of new HB treatment modalities with respect to FIX assay performance.
Aim: To further characterise variability in FIX activity measured using different one-stage assays (OSAs) and chromogenic assays (CAs) in patients with HB receiving gene therapy utilising the FIX Padua variant and to assess whether assay differences were due to the FIX-Padua variant.
Diabetes Res Clin Pract
May 2025
Endeavor Health (NorthShore Hospitals), Skokie, IL, USA. Electronic address:
Aims: To assess the association between remaining persistent with once-weekly glucagon-like peptide-1 receptor agonists (OW GLP-1 RAs) and the risk of major adverse cardiovascular events (MACE) among patients with type 2 diabetes mellitus (T2DM) and atherosclerotic cardiovascular disease (ASCVD).
Methods: We used the Optum Research Database to identify patients who initiated OW GLP-1 RAs between 1/1/2018-11/30/2022. Patients were classified as persistent or non-persistent depending on whether there was a ≥ 60-day gap in medication supply after they continuously used the medication for the first three months.
Adv Sci (Weinh)
April 2025
CRB Trieste, Bracco Imaging SpA, AREA Science Park, Basovizza, 34149, TS, Italy.
Magnetic Resonance Imaging (MRI) plays a vital role in the accurate diagnosis of numerous human diseases and disorders, with Gd(III)-based contrast agents (GBCAs) being used in ≈30%-40% of procedures, resulting in ≈30 million doses administered annually worldwide. The careful design of a rigid macrocyclic chelator featuring a highly hydrophilic periphery leads to the development of gadopiclenol, the first bis-hydrated Gd(III)-based MRI contrast agent, recently approved for clinical use by both the FDA and EMA. The stereochemistry of the coordinating arms is found to play a crucial role in the remarkable thermodynamic stability and inertness of the Gd(III)-complex with the RRR/SSS-stereoisomer of this heptadentate chelating agent, ensuring its safety in vivo.
View Article and Find Full Text PDFSarcoidosis Vasc Diffuse Lung Dis
June 2024
Pulmonary institute, Soroka university medical center, Beer sheva, Israel.
Background And Aim: Sarcoidosis is a systemic disease of unknown etiology with diverse clinical manifestations. Disease may resolve spontaneously or require immunosuppression to control progression. Currently, there is no predictive model to direct treatment, and management is guided by symptoms and functional impairment.
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