9 research outputs found
Acetylcholinesterase inhibitors and risk of bleeding and acute ischemic events in non-hypertensive Alzheimer’s patients
Introduction: Acetylcholinesterase inhibitors (AChEIs) are commonly used to treat
mild to moderate cases of Alzheimer disease (AD). To the best of our knowledge, there
has been no study estimating the risk of bleeding and cardiovascular events in patients
with non-hypertensive AD. Therefore, this study aimed to estimate the association
between AChEIs and the risk of bleeding and cardiovascular ischemic events in patients
with non-hypertensive AD.
Methods: A nested case-control study was conducted to estimate the risk of bleeding
and ischemic events (angina, myocardial infarction [MI], and stroke) in patients with
AD. This study was conducted using the UK Clinical Practice Research Datalink and
Hospital Episode Statistics (HES) databases. The study cohort consisted of AD patients
≥65 years of age. The case groups included all AD subjects in the database who had
a bleeding or ischemic event during the cohort follow-up. Four controls were selected
for each case. Patients were classified as current users or past users based on a 60-day
threshold of consuming the drug. Simple and multivariable conditional logistic regression analyses were used to calculate the adjusted odds ratio for bleeding events and
cardiovascular events.
Results: We identified 507 cases and selected 2028 controls for the bleeding event
cohort and 555 cases and 2220 controls for the ischemic event cohort. The adjusted
odds ratio (OR) (95% confidence interval [CI]) for the association of AChEI use was 0.93
(0.75 to 1.16) for bleeding events, 2.58 (1.01 to 6.59) for angina, and 1.89 (1.07 to 3.33)
for MI. Past users of AChEIs were also at increased risk of stroke (1.51 [1.00 to 2.27]).
Discussion: This is the first study assessing the risk of bleeding and cardiovascular
events in patients with non-hypertensive AD. Our findings could be of great interest
for clinicians and researchers working on AD
Patterns of antibiotic use and risk of hospital admission because of Clostridium difficile infection
Barriers to enrollment of patients with recurrent diffuse large B-cell lymphoma onto clinical trials
Barriers and facilitators of skin self-examination among patients diagnosed with melanoma
observational study with longitudinal follow-up assessing predictors of skin self-examination in patients with melanom
Short and long-term barriers and facilitators of skin self-examination among individuals diagnosed with melanoma
Abstract
Background
Melanoma can be lethal if not detected early and treated. Early detection can be facilitated via skin self-examination (SSE) and as such, SSE is part of melanoma follow-up care for individuals with a prior history, who face a life-long risk of reoccurrence. The objective of the current study was to identify short- and long-term predictors of SSE among melanoma survivors to inform future prevention interventions in high-risk groups.
Method
This is an observational study with longitudinal assessments conducted with adult melanoma patients in active follow-up care.
Primary outcome measures
Behavioral outcomes, comprehensive SSE (checking up to 5 body areas in the last 3 months) and optimal SSE (checking the entire body at least monthly in the last 3 months) were assessed at 3, 12, and 24 months post a dermatological educational session on skin cancer prevention. T tests and chi square analyses were used to examine changes in outcomes from 3 to 12 and 24 months. Linear and logistic regression models were used to examine the association between predictors and the primary outcomes.
Results
Comprehensive SSE did not decrease significantly from 3 (M = 2.7, SD = 1.1) to 12 (M = 2.6, SD = 1.2) and 24 months (M = 2.4, SD = 1.2) post the education session, with the stronger predictor at all timepoints being intentions to perform SSE. Optimal SSE was higher at 3 months (59%) compared to 12 (46%) and 24 months (34%), with key predictors including self-efficacy and intentions to perform SSE and male sex at 3 months post; self-efficacy and reliance on medical advice at 12 months; and (lower) education and self-efficacy at 24 months.
Conclusions
The key findings of this study are that 1) survivors maintain SSE behaviour over time, but rates of SSE performed in agreement with medical recommendations are higher immediately post standard dermatological education (i.e. usual care) and decrease somewhat over a 24-month period; and 2) the strongest psycho-social predictors of SSE are intentions and self-efficacy to perform the behavior, which are highly modifiable, for example via motivational interviewing and goal setting health interventions