Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 84
Filter
2.
J Fam Pract ; 71(10): 442-444, 2022 12.
Article in English | MEDLINE | ID: mdl-36735947

ABSTRACT

There are modest effects on depression but not anxiety. Gender-affirming hormone therapy (GAHT) is associated with modest improvements in standardized scores for quality of life (QOL) and depression in adult male-to-female and female-to-male transgender people and modest improvements in depression scores in transgender adolescents, but the effect on anxiety is uncertain (strength of recommendation [SOR]: B, based on a preponderance of low-quality prospective cohort studies with inconsistent results). GAHT is associated with reduced gender dysphoria and decreased suicidality (SOR: B, based on a prospective cohort study). However, there is insufficient evidence to determine any effect on suicide completion. No studies associated GAHT with worsened QOL, depression, or anxiety scores.


Subject(s)
Transgender Persons , Transsexualism , Adult , Adolescent , Humans , Male , Female , Prospective Studies , Quality of Life , Hormones
3.
J Fam Pract ; 70(5): 253-255, 2021 Jun.
Article in English | MEDLINE | ID: mdl-34410919

ABSTRACT

PROBABLY, although there are no head-to-head trials comparing the 2 dosing regimens. Event-driven pre-exposure prophylaxis (PrEP) dosing reduces HIV conversion by 86% compared to placebo (strength of recommendation [SOR]: B, large randomized controlled trial [RCT]). Daily PrEP reduces HIV conversion by 44% to 86% (SOR: B, based on open-label RCTs).Event-driven PrEP regimens may be associated with lower adherence when compared with daily PrEP regimens (average of 70% for event-driven PrEP vs average of 92% for daily PrEP) (SOR: B, based on open-label and cohort trials). Event-driven PrEP regimens have lower medication costs, and they are associated with no difference in the rate of sexually transmitted infections (STIs) (SOR: B, based on prospective cohort studies). Patients may prefer them to daily regimens (75% choose event driven PrEP vs 25% choose daily PrEP) (SOR: BB, based on the preponderance of prospective cohort studies with conflicting results).


Subject(s)
Dose-Response Relationship, Drug , HIV Infections/drug therapy , Pre-Exposure Prophylaxis/methods , Humans , Pre-Exposure Prophylaxis/statistics & numerical data
4.
J Fam Pract ; 70(3): E1-E3, 2021 04.
Article in English | MEDLINE | ID: mdl-34314342

ABSTRACT

MAYBE, but it's too soon to tell. There is limited evidence that ketamine by itself is effective in the very short term. Single-dose intravenous (IV) ketamine is more likely than placebo (odds ratio = 11-13) to produce improvement (> 50%) in standardized depression scores in 1 to 3 days, lasting up to a week. Twice- or thriceweekly IV ketamine improves symptom scores by 20%-25% over 2 weeks (strength of recommendation [SOR]: B, meta-analysis of small, low-quality, randomized controlled trials [RCTs] and a single small RCT).Augmentation of sertraline with daily oral ketamine moderately improves symptom scores for 6 weeks in patients with moderate depression (SOR: B, small, lowquality RCTs).Augmentation of oral antidepressants (duloxetine, escitalopram, sertraline, venlafaxine) with intranasal esketamine spray improves response and remission rates at 4 weeks (16% for both outcomes) in patients with predominantly treatment-resistant major depression (SOR: A, meta-analysis of RCTs).Ketamine therapy is associated with confusion, emotional blunting, headache, dizziness, and blurred vision (SOR: A, metaanalyses).Nasal esketamine spray produces the adverse effects of dizziness, vertigo, and blurred vision severe enough to cause discontinuation in 4% of patients; it also can produce transient elevation of blood pressure (SOR: A, meta-analyses).


Subject(s)
Antidepressive Agents/adverse effects , Depressive Disorder, Treatment-Resistant/drug therapy , Ketamine/adverse effects , Administration, Intranasal , Administration, Oral , Adult , Antidepressive Agents/therapeutic use , Depression/drug therapy , Depressive Disorder, Treatment-Resistant/prevention & control , Drug Administration Schedule , Humans , Ketamine/therapeutic use , Remission Induction , Treatment Outcome
5.
Am Fam Physician ; 103(7): 434-436, 2021 04 01.
Article in English | MEDLINE | ID: mdl-33788516
6.
J Fam Pract ; 70(2): 100-101, 2021 03.
Article in English | MEDLINE | ID: mdl-33760905

ABSTRACT

YES, TO SOME DEGREE-BUT IT IS OF UNCERTAIN CLINICAL SIGNIFICANCE. OVER A PERIOD OF 6 MONTHS, METFORMIN MODESTLY REDUCED WEIGHT (-2.1 KG) AND BODY FAT MASS (-1.9%), BUT NOT BODY MASS INDEX (BMI) OR LEAN BODY MASS, IN ADOLESCENTS WHO WERE OVERWEIGHT OR OBESE. THIS IS COMPARABLE TO LIFESTYLE INTERVENTIONS (DIET AND EXERCISE) SUPPORTED WITH > 26 HOURS OF COUNSELING, WHICH MODESTLY IMPROVED BMI BUT NOT WEIGHT. (STRENGTH OF RECOMMENDATION [SOR]: A, BASED ON A LARGE META-ANALYSIS OF RANDOMIZED CONTROLLED TRIALS [RCTS] OF VARIABLE QUALITY).


Subject(s)
Metformin/therapeutic use , Pediatric Obesity/drug therapy , Adolescent , Body Mass Index , Body Weight/drug effects , Humans , Hypoglycemic Agents/adverse effects , Hypoglycemic Agents/therapeutic use , Metformin/adverse effects , Systematic Reviews as Topic
9.
J Fam Pract ; 69(6): 309;310;315, 2020.
Article in English | MEDLINE | ID: mdl-32724912

ABSTRACT

No. Adding a proton pump inhibitor (PPI) in patients taking antiplatelet medications such as clopidogrel for acute coronary syndrome (ACS) doesn't increase the composite risk of cardiovascular (CV) events: CV death, myocardial infarction (MI), and cerebrovascular accident (CVA) (strength of recommendation: B, randomized, controlled trial [RCT] and prepon-derance of posthoc analyses of large RCTs).


Subject(s)
Acute Coronary Syndrome/drug therapy , Cardiovascular Diseases/etiology , Clopidogrel/adverse effects , Proton Pump Inhibitors/adverse effects , Acute Coronary Syndrome/physiopathology , Aged , Aspirin/adverse effects , Aspirin/therapeutic use , Cardiovascular Diseases/physiopathology , Clopidogrel/therapeutic use , Double-Blind Method , Drug Interactions , Drug-Related Side Effects and Adverse Reactions , Female , Humans , Male , Middle Aged , Omeprazole/adverse effects , Omeprazole/therapeutic use , Platelet Aggregation Inhibitors/adverse effects , Platelet Aggregation Inhibitors/therapeutic use , Proton Pump Inhibitors/therapeutic use , Treatment Outcome
12.
J Fam Pract ; 68(10): E12-E13, 2019 12.
Article in English | MEDLINE | ID: mdl-31860706

ABSTRACT

Probably. Electronic cigarette (e-cigarette) use by adolescents is associated with a 2- to 4-fold increase in cigarette smoking over the next year (strength of recommendation: A, meta-analysis and subsequent prospective cohort studies).


Subject(s)
Adolescent Behavior/psychology , Cigarette Smoking/psychology , Vaping/adverse effects , Vaping/psychology , Adolescent , Cohort Studies , Electronic Nicotine Delivery Systems , Female , Humans , Male , Prospective Studies , Risk Factors
18.
J Fam Pract ; 67(4): 249-251, 2018 04.
Article in English | MEDLINE | ID: mdl-29614148

ABSTRACT

Quite well, for cardiopulmonary resuscitation (CPR). Most patients (91%-100%) who select "do not resuscitate" (DNR) on their physician's orders for life-sustaining treatment (POLST) forms are allowed a natural death without attempted CPR across a variety of settings (community, skilled nursing facilities, emergency medical services, and hospice). Few patients (6%) who select "comfort measures only" die in the hospital, whereas more (22%) who choose "limited interventions," and still more (34%) without a POLST form, die in the hospital (strength of recommendation [SOR]: B, large, consistent cross-sectional and cohort studies).


Subject(s)
Advance Care Planning/standards , Advance Directives/statistics & numerical data , Delivery of Health Care/standards , Guideline Adherence/standards , Life Support Care/standards , Terminal Care/standards , Advance Care Planning/statistics & numerical data , Aged , Cohort Studies , Cross-Sectional Studies , Delivery of Health Care/statistics & numerical data , Female , Guideline Adherence/statistics & numerical data , Humans , Life Support Care/statistics & numerical data , Male , Terminal Care/statistics & numerical data , United States
19.
Am Fam Physician ; 96(9): 565-566, 2017 11 01.
Article in English | MEDLINE | ID: mdl-29094885
20.
J Fam Pract ; 66(7): 462-466, 2017 Jul.
Article in English | MEDLINE | ID: mdl-28700762

ABSTRACT

The effects are unclear. Marijuana use during pregnancy is associated with clinically unimportant lower birth weights (growth differences of approximately 100 g), but no differences in preterm births or congenital anomalies.


Subject(s)
Cannabis/adverse effects , Fetal Development/drug effects , Marijuana Smoking/adverse effects , Prenatal Exposure Delayed Effects/chemically induced , Abnormalities, Drug-Induced/epidemiology , Female , Humans , Infant, Newborn , Marijuana Smoking/epidemiology , Pregnancy
SELECTION OF CITATIONS
SEARCH DETAIL
...