Publications by authors named "L Carl"

Background: Public reporting is supposed to be helpful in differentiating between well and poorly performing nursing homes; however, hospital patients often have difficulties to deal with quality information. Discharge planners (DP) can support them in comparing quality and, by influencing patients' decision, lead to better provision of care in nursing homes.

Objective: This study investigated the choice behavior of DP, their use of quality information and the potential to impact the decision-making of patients.

View Article and Find Full Text PDF
Article Synopsis
  • Pain is a leading reason for medical visits, yet the root causes remain inadequately addressed despite available analgesics and research on antioxidants like L-ascorbate.
  • The study evaluated literature on the therapeutic effects of L-ascorbate (vitamin C) across various pain conditions, aiming to create specific guidance for its intravenous use.
  • Findings suggested L-ascorbate is effective for several pain types, including inflammatory pain and neuropathic pain, but results varied due to differences in administration methods, dosages, and study quality.
View Article and Find Full Text PDF

Purpose: High volumes of chest radiographs (CXR) remain uninterpreted due to severe shortage of radiologists. These CXRs may be informally reported by non-radiologist physicians, or not reviewed at all. Artificial intelligence (AI) software can aid lung nodule detection.

View Article and Find Full Text PDF

Objective: Haemophagocytic lymphohistiocytosis (HLH) and macrophage activation syndrome (MAS) are life-threatening systemic hyperinflammatory syndromes that can develop in most inflammatory contexts. They can progress rapidly, and early identification and management are critical for preventing organ failure and mortality. This effort aimed to develop evidence-based and consensus-based points to consider to assist clinicians in optimising decision-making in the of diagnosis, treatment and monitoring of HLH/MAS.

View Article and Find Full Text PDF

Objective: Haemophagocytic lymphohistiocytosis (HLH) and macrophage activation syndrome (MAS) are life-threatening systemic hyperinflammatory syndromes that can develop in most inflammatory contexts. They can progress rapidly, and early identification and management are critical for preventing organ failure and mortality. This effort aimed to develop evidence-based and consensus-based points to consider to assist clinicians in optimising decision-making in the early stages of diagnosis, treatment and monitoring of HLH/MAS.

View Article and Find Full Text PDF