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1.
Expert Opin Investig Drugs ; 29(9): 893-900, 2020 Sep.
Article in English | MEDLINE | ID: mdl-32746636

ABSTRACT

INTRODUCTION: Vulvovaginal candidiasis (VVC) is a common fungal infection caused by predominantly Candida albicans, and is diagnosed in up to 40% of women with vaginal complaints in the primary care setting. Approximately 75% of women experience at least one episode during their reproductive years. AREAS COVERED: Ibrexafungerp is an orally active, semi-synthetic triterpenoid glucan synthase inhibitor under development for treatment and prevention of VVC. We present the chemistry, mechanism of action, pharmacology, microbiology, and results from clinical studies with ibrexafungerp in women with VVC. EXPERT OPINION: Ibrexafungerp addresses several unmet needs with existing antifungal drugs as a first in a new class of antifungal agents with a novel mechanism of action demonstrating no antifungal cross resistance with azoles, and fungicidal activity against Candida spp., including fluconazole-resistant species. Some of the key attributes of ibrexafungerp related to VVC include oral one-day dosing, high tissue penetration, enhanced activity at low pH seen in the vagina, low risk for clinically significant drug-drug interactions, and a low risk of adverse events. If approved, ibrexafungerp will be the first new antifungal agent available for the treatment of VVC in more than 20 years and the only oral, non-azole antifungal approved for women suffering from VVC.


Subject(s)
Antifungal Agents/administration & dosage , Candidiasis, Vulvovaginal/drug therapy , Glycosides/administration & dosage , Triterpenes/administration & dosage , Animals , Antifungal Agents/adverse effects , Antifungal Agents/pharmacology , Candida/drug effects , Candida/isolation & purification , Candidiasis, Vulvovaginal/microbiology , Drug Administration Schedule , Drug Interactions , Drug Resistance, Fungal , Female , Glycosides/adverse effects , Glycosides/pharmacology , Humans , Triterpenes/adverse effects , Triterpenes/pharmacology
2.
Nurs Womens Health ; 22(5): 423-430, 2018 Oct.
Article in English | MEDLINE | ID: mdl-30170002

ABSTRACT

Genitourinary syndrome of menopause (GSM), formerly referred to as vulvovaginal atrophy or atrophic vaginitis, is a common chronic condition that requires a collaborative treatment plan between a health care provider and a woman to relieve symptoms and improve quality of life. Many women are not aware that symptoms can be controlled with treatment. Current treatment options approved for GSM include vaginal moisturizers, lubricants, and hormones. For women with GSM symptoms that are unresponsive to nonhormonal therapy, low-dose vaginal estrogen therapy is the preferred pharmacologic treatment. Clinicians should be trained to routinely ask appropriate questions during the history to elicit sufficient information to assess for GSM. Physical examination findings may further confirm suspicion of GSM.


Subject(s)
Atrophic Vaginitis/diagnosis , Atrophic Vaginitis/therapy , Menopause , Female , Humans , Middle Aged , Syndrome
3.
J Am Acad Nurse Pract ; 19(8): 427-37, 2007 Aug.
Article in English | MEDLINE | ID: mdl-17655572

ABSTRACT

PURPOSE: To evaluate the benefits and risks of hormone therapy (HT) and other treatment options for early postmenopausal women. DATA SOURCES: Published clinical trials, selected peer-reviewed literature, and recent clinical practice guidelines. CONCLUSIONS: Results of the Women's Health Initiative (WHI) studies on HT may not be directly applicable to healthy, early postmenopausal women suffering from hot flushes. HT is the most effective treatment for menopausal symptoms. The benefits of HT in relieving menopausal symptoms are likely to exceed the risks in this population. IMPLICATIONS FOR PRACTICE: The results of the WHI reinforce the importance of individualized care based on a woman's medical history, medical needs, and desired outcomes. Nurse practitioners can help their patients put recent results into perspective. When HT is used, nurse practitioners should consider using lower doses and reevaluate the need for therapy annually.


Subject(s)
Estrogen Replacement Therapy , Menopause , Nurse Practitioners/organization & administration , Nurse's Role , Attitude of Health Personnel , Counseling , Estrogen Replacement Therapy/adverse effects , Estrogen Replacement Therapy/methods , Female , Humans , Life Style , Medical History Taking , Menopause/drug effects , Menopause/physiology , Menopause/psychology , Nurse Practitioners/psychology , Nurse's Role/psychology , Nursing Assessment , Patient Care Planning , Patient Education as Topic , Patient Selection , Practice Guidelines as Topic , Primary Health Care/organization & administration , Risk Assessment , Risk Factors , Risk Reduction Behavior , Safety , Women's Health
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