News & Updates
Filter by Specialty:
Infliximab, vedolizumab similarly effective as 1L Tx for paediatric IBD
In a study presented at Crohn’s and Colitis Congress 2024, infliximab and vedolizumab were found to have similar effectiveness in achievĀing steroid-free clinical remission (SFCR) and biochemical remission (BR) at 12 months when used as first-line treatment for biologic-naïve paediatric patients with unĀcomplicated mild-to-moderately active inflammatory bowel disease (IBD).
Infliximab, vedolizumab similarly effective as 1L Tx for paediatric IBD
22 Feb 2024Well-managed blood sugar through multidisciplinary care can stave off dementia in T2D patients
A multidisciplinary intervention program for type 2 diabetes (T2D) in the primary care setting subsequently reduces the incidence of dementia, as reported in a study.
Well-managed blood sugar through multidisciplinary care can stave off dementia in T2D patients
21 Feb 2024SG Framingham Risk Score needs recalibration to improve prediction accuracy
Current guidelines that are being used in Singapore (SG) for predicting cardiovascular disease (CVD) must be updated to improve risk prediction accuracy. This can be done by recalibrating risk functions and employing wearable metrics that provide a huge amount of objective health data, suggests a study.
SG Framingham Risk Score needs recalibration to improve prediction accuracy
21 Feb 2024Dexmedetomidine use raises body temp in ICU patients with obesity
Critically ill patients with obesity see a significant rise in their body temperature following the use of dexmedetomidine (DEX) for ongoing sedation, as shown in a recent study. Furthermore, DEX duration and baseline temperature are significantly associated with fever development in these individuals.
Dexmedetomidine use raises body temp in ICU patients with obesity
20 Feb 2024Reteplase a good alternative to alteplase in acute ischaemic stroke
Treatment with reteplase appears more effective than alteplase in patients with acute ischaemic stroke (AIS) who have been treated within 4.5 hours of symptom onset, according to the results of RAISE, a phase III multicentre, open-label, randomized controlled, noninferiority trial.