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1.
Crit Care ; 27(1): 29, 2023 01 20.
Article in English | MEDLINE | ID: mdl-36670410

ABSTRACT

Vasopressors and fluids are the cornerstones for the treatment of shock. The current international guidelines on shock recommend norepinephrine as the first-line vasopressor and vasopressin as the second-line vasopressor. In clinical practice, due to drug availability, local practice variations, special settings, and ongoing research, several alternative vasoconstrictors and adjuncts are used in the absence of precise equivalent doses. Norepinephrine equivalence (NEE) is frequently used in clinical trials to overcome this heterogeneity and describe vasopressor support in a standardized manner. NEE quantifies the total amount of vasopressors, considering the potency of each such agent, which typically includes catecholamines, derivatives, and vasopressin. Intensive care studies use NEE as an eligibility criterion and also an outcome measure. On the other hand, NEE has several pitfalls which clinicians should know, important the lack of conversion of novel vasopressors such as angiotensin II and also adjuncts such as methylene blue, including a lack of high-quality data to support the equation and validate its predictive performance in all types of critical care practice. This review describes the history of NEE and suggests an updated formula incorporating novel vasopressors and adjuncts.


Subject(s)
Shock, Septic , Shock , Humans , Norepinephrine/pharmacology , Norepinephrine/therapeutic use , Shock, Septic/drug therapy , Shock/drug therapy , Vasoconstrictor Agents/pharmacology , Vasoconstrictor Agents/therapeutic use , Vasopressins/therapeutic use , Critical Care
2.
J Nerv Ment Dis ; 204(9): 717-22, 2016 09.
Article in English | MEDLINE | ID: mdl-27570901

ABSTRACT

Patients benefit from the presence of empathic caregivers (CGs). In this regard, empathy toward the patient is one of the clinical targets for improving patient outcomes. However, relatively little is known about the impact of patients' empathic responses on the CGs' burden. Among people living with Parkinson's disease (PwP), care partners play a major role. This study involved 28 spouse-patient couples. Empathy, stress burden, and mood disorders (such as anxiety and depression) were assessed over a 6-month period, before and after the reported intervention. Our observation points out that the improvement of patient empathy is necessary for a significant burden reduction among spouses caring for PwP.


Subject(s)
Caregivers/psychology , Empathy , Aged , Anxiety/etiology , Depression/etiology , Female , Humans , Male , Parkinson Disease/psychology , Parkinson Disease/therapy , Psychiatric Status Rating Scales , Spouses/psychology , Stress, Psychological/etiology
3.
Ageing Res Rev ; 10(1): 124-31, 2011 Jan.
Article in English | MEDLINE | ID: mdl-20920611

ABSTRACT

The assumption that disease specific risk factors are similar or the same in men and women may lead to incorrect primary prevention strategies. This study focused on the evaluation of gender-specific Alzheimer's disease (AD) risk factors. In AD, female gender appears to be an important risk factor associated with the aberrant production of beta amyloid (ßA) peptides. Although decreased levels in plasma DHA concentration are associated with cognitive decline in healthy elderly and Alzheimer's patients, pre-treatment with DHA significantly reduced the survival of cortical neurons incubated with beta amyloid (ßA). Hence, in the presence of an increasing amount of ßA, paradoxically women - who have higher plasma levels of DHA - are more likely to develop AD. Aspirin (ASA) converts cyclooxygenase (COX)-2 into a form that generates new neuroprotective docosanoids from DHA; therefore, ASA might positively resolve the paradoxical effect of the concomitant presence of DHA and ßA.


Subject(s)
Alzheimer Disease/prevention & control , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Aspirin/therapeutic use , Docosahexaenoic Acids/therapeutic use , Aged , Alzheimer Disease/genetics , Amyloid beta-Peptides/metabolism , Apolipoproteins E/genetics , Brain-Derived Neurotrophic Factor/metabolism , Female , Hippocampus/pathology , Humans , Neocortex/pathology , Neural Pathways/pathology , Peroxisome Proliferator-Activated Receptors/genetics , Risk Factors , Women
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