Erectile Dysfunction Lower In Men Who Have Intercourse More Often


By sciencedaily.com

Having intercourse more often may help prevent the development of erectile dysfunction (ED). A new study reports that researchers have found that men who had intercourse more often were less likely to develop ED.

Analyzing a five-year study of 989 men aged 55 to 75 years from Pirkanmaa, Finland, the investigators observed that men reporting intercourse less than once per week at baseline had twice the incidence of erectile dysfunction compared with those reporting intercourse once per week. Further, the risk of erectile dysfunction was inversely related to the frequency of intercourse.

Other factors that may affect the incidence of ED, such as age, chronic medical conditions (diabetes, heart disease, hypertension, cerebrovascular disease and depression), body mass index and smoking were included in the analysis of the data.

Erectile dysfunction incidence was 79 cases per 1000 in men who had reported sexual intercourse less than once per week, dropping to 32 cases per 1000 in men reporting intercourse once per week and falling further to 16 per 1000 in those reporting intercourse 3 or more times per week.

In addition, the frequency of morning erections predicted the development of complete erectile dysfunction, with an approximate 2.5-fold risk among those with less than 1 morning erection per week compared with 2 to 3 morning erections per week

Writing in the article, Juha Koskimäki, MD, PhD, Tampere University Hospital, Department of Urology, Tampere, Finland, states; "Regular intercourse has an important role in preserving erectile function among elderly men, whereas morning erection does not exert a similar effect. Continued sexual activity decreases the incidence of erectile dysfunction in direct proportion to coital frequency."

The study clearly indicates that regular intercourse protects men from the development of erectile dysfunction, which may, in turn, impact general health and quality of life. The investigators advise clinicians to support the sexual activity of their patients.

Source: https://www.sciencedaily.com/releases/2008/07/080702091346.htm

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Sunday, May 10, 2026

Amitriptyline Treatment Decisions: Selecting the Right Dose for Depression, Pain, or Sleep

Amitriptyline is used across a wider dose range than almost any other psychiatric or pain medication in clinical practice, and the dose selected depends entirely on the clinical indication and the patient's individual tolerability. Understanding why prescribers choose particular doses and how they adjust them helps patients engage constructively with their treatment. For major depressive disorder, effective doses are typically in the range of 75 to 150 mg per day, though some patients require doses up to 200 to 300 mg per day when lower doses do not adequately control symptoms. These doses are substantially higher than what is used for pain or sleep applications. Prescribers usually begin at 25 to 50 mg once daily at bedtime and increase gradually every one to two weeks as tolerability is assessed, because the anticholinergic and sedating effects are most pronounced when therapy begins and often attenuate over two to three weeks of continued use. For chronic pain indications including neuropathic pain, fibromyalgia, and chronic headache, doses of 10 to 25 mg at bedtime are standard starting and often maintenance doses. At these low doses, the antidepressant mechanism is not the primary therapeutic driver. The pain-modulating effects appear to operate through sodium channel stabilization and central sensitization pathways at subanesthetic drug levels. Patients prescribed 10 mg for chronic pain should understand they are receiving a different therapeutic application than the antidepressant indication, and they should not assume their provider has made an error in prescribing. Migraine prevention regimens typically use 10 to 50 mg nightly, with dose titration based on headache frequency response over a period of six to eight weeks. Multiple preventive medication trials are often conducted sequentially before a patient settles on the most effective preventive agent. Monitoring during amitriptyline therapy for depression includes symptom assessment, weight, and for higher-dose regimens, consideration of periodic electrocardiogram to assess QTc interval. Amitriptyline prolongs cardiac repolarization in a dose-dependent manner, which is relevant more at antidepressant doses than at chronic pain doses. Older patients require particular caution. Amitriptyline appears on the Beers Criteria list of medications to use with caution in older adults due to its anticholinergic properties, fall risk from orthostatic hypotension, and potential cognitive effects from central acetylcholine blockade. Abrupt discontinuation of amitriptyline after extended use at antidepressant doses can cause withdrawal symptoms including rebound anxiety, sweating, and gastrointestinal distress. Dose tapering over weeks is standard practice when discontinuing. For patients who want to understand the dose and monitoring logic behind their amitriptyline prescription, reviewing information about elavil-amitriptyline treatment decisions provides important clinical context. For patients comparing amitriptyline to other antidepressant options and how tricyclic drugs compare to newer agents, antidepressant medication category resources offers a helpful comparative perspective.

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