Mashup Score:1
HCPLive®Greater Hydroxyurea Doses, Adherence Linked to Improved Pediatric Sickle Cell Anemia Outcomes - 1 month
Mashup Score:1
Mashup Score:1
HCPLive®Greater Hydroxyurea Doses, Adherence Linked to Improved Pediatric Sickle Cell Anemia Outcomes - 1 month
Mashup Score:1
Mashup Score:1
HCPLive®Exercise Testing is Viable for Stable Sickle Cell Patients - 1 month
Mashup Score:1
A new study evaluates the prognostic potential of exercise testing for patients with sickle cell...
While exercise testing is often used as a prognostic marker in cardiovascular disease, the evidence surrounding exercise in patients with SCD is lacking. #SickleCell #SCD #RareDisease https://t.co/mHsP1gIWbK - view on twitter
Mashup Score:1
HCPLive®Non-Opioid Painkiller ACP-044 Fails to Meet Endpoint in Phase 2 Acute Pain Trial - 1 month
Mashup Score:1
Acadia Pharmaceuticals evaluated the effects of its novel redox modulator drug on pain intensity levels of patients undergoing a...
ACP-044 is also being examined for its role in treating pain associated with osteoarthritis of the knee in a phase 2 trial that's expected to conclude in the first half of 2023. #nonopioid #Rheum #Pain https://t.co/t5fMvZtFmI - view on twitter
Investigators address the need for understanding surrounding the relationship between poor bone health and patients who are hemophilia carriers and those with von Willebrand...
Investigators call for more research on poor bone health in patients with hemophilia, von Willebrand disease, and those who are hemophilia carriers. #HemophiliaDay #BleedingDisorder #Rheum https://t.co/MWI62N7TVY - view on twitter
Guidelines lack clear recommendations for osteoporosis management and fall prevention, which may be due to a lack of evidence in the...
A review of current #hemophilia guidelines found all contained inadequate recommendations for osteoporosis management and fall prevention in patients with hemophilia. https://t.co/zGAZk3hksj - view on twitter
A systematic literature review highlighted key risk factors that could constitute a risk assessment model for hemophilia bleeding—a currently lacking guidance for...
A bleeding risk assessment model for #hemophilia is presently lacking. But investigators from @McMasterU uncovered factors that would likely influence such clinical guidance: https://t.co/wduFYOixdg - view on twitter
Voxelotor is the first and only FDA-approved medication for children with sickle cell...
Voxelotor targets sickle hemoglobin polymerization. Read more about the HOPE-KIDS 1 trial just published in Pediatrics Blood & Cancer. #SCD #Oxbryta https://t.co/xPZJR1fQ83 - view on twitter
This episode features a conversation with Dr. Amelle Shillington and Jacob and Ashley Wiley after Shillington diagnosed the extremely rare genetic disease that’s afflicted...
This month, we focus on a disease with 70 documented cases worldwide and welcomed 3 guests to discuss the diagnosis of TANGO2 in 15-month old Aislynn Wiley. Listen to her story through her parents & Dr. Amelle Shillington @CincyChildrens @TANGO2Research https://t.co/t29B0qYP6p https://t.co/t29B0qYP6p - view on twitter
A study highlights methods to define hydroxyurea exposure as means of understanding hematologic benefit derived from the first-line drug for...
How can we begin to optimize hydroxyurea use among children with #SickleCell #anemia? Start off by better defining what "exposure" to the drug looks like: https://t.co/4lBlkSyCri - view on twitter