Discontinuing SSRIs or SNRIs during pregnancy was associated with nearly double the risk of mental health emergencies, according to a cross-sectional analysis of 3,983 women. While prepregnancy psychiatric visit rates were similar between groups, antidepressant discontinuation was linked to significantly higher emergency department visits for psychiatric indications, particularly during the first and ninth months of pregnancy. These findings highlight the maternal risks of routine antidepressant discontinuation and reinforce the importance of individualized risk–benefit counseling during pregnancy.
Team SunilMadhavs World
- OBSTETRICSPSYCHIATRY < class="penci-entry-title entry-title grid-title penci_grid_title">Antidepressant discontinuation during pregnancy raises risk for mental health emergencies>
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A large UK Biobank analysis found that higher serum vitamin D levels were associated with a lower risk of hospitalization for respiratory tract infections, while severe deficiency increased risk. Although causality remains unproven, the findings position vitamin D status as a potentially modifiable factor in preventive health strategies.
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Statin Therapy and Risk of Acute Exacerbations in Adults With Mild Asthma Background Statins, widely prescribed for cardiovascular disease prevention, exhibit pleiotropic effects that extend beyond lipid lowering. …
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FDA Restrictions on Non-Approved GLP-1 API Use and Marketing The US Food and Drug Administration (FDA) has announced plans to implement restrictions on the use of glucagon-like peptide-1 (GLP-1) …
- Cardiology < class="penci-entry-title entry-title grid-title penci_grid_title">Urate treatment reduces cardiovascular risk in patients with gout>
Association Between Target Urate Levels and Cardiovascular Outcomes in Gout Data published in JAMA Internal Medicine indicates that patients with gout who successfully achieve a serum urate level of …
- Cardiology < class="penci-entry-title entry-title grid-title penci_grid_title">FDA clears investigational new drug application for ER-100>
A novel cellular rejuvenation therapy, ER-100, has received clearance from the U.S. Food and Drug Administration (FDA) to proceed with human clinical testing, marking what the sponsor describes as …
- Cardiology < class="penci-entry-title entry-title grid-title penci_grid_title">4-hour dialysis treatments improve outcomes>
Patients undergoing maintenance hemodialysis continue to experience disproportionately high mortality and substantial treatment-related burden. Among the modifiable aspects of dialysis care, treatment duration represents a potentially powerful yet underused lever …
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Excerpt:
The FDA has granted approval to Novartis for Itvisma (onasemnogene abeparvovec-brve), the first gene replacement therapy for spinal muscular atrophy (SMA) available for patients aged 2 years and older. Backed by data from the Phase 3 STEER and Phase 3b STRENGTH trials, this one-time intrathecal treatment addresses the genetic root cause of SMA and is expected to be available in the U.S. this December.
