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  1. Article ; Online: Risk of Gastrointestinal Adverse Events Associated With Glucagon-Like Peptide-1 Receptor Agonists for Weight Loss.

    Sodhi, Mohit / Rezaeianzadeh, Ramin / Kezouh, Abbas / Etminan, Mahyar

    JAMA

    2023  Volume 330, Issue 18, Page(s) 1795–1797

    MeSH term(s) Humans ; Diabetes Mellitus, Type 2/drug therapy ; Glucagon-Like Peptide-1 Receptor/agonists ; Glucagon-Like Peptides ; Hypoglycemic Agents/adverse effects ; Hypoglycemic Agents/therapeutic use ; Liraglutide/adverse effects ; Liraglutide/therapeutic use ; Weight Loss/drug effects ; Anti-Obesity Agents/adverse effects ; Anti-Obesity Agents/pharmacology ; Anti-Obesity Agents/therapeutic use ; Overweight/drug therapy ; Gastrointestinal Diseases/chemically induced
    Chemical Substances Glucagon-Like Peptide-1 Receptor ; Glucagon-Like Peptides (62340-29-8) ; Hypoglycemic Agents ; Liraglutide (839I73S42A) ; Anti-Obesity Agents
    Language English
    Publishing date 2023-10-05
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2958-0
    ISSN 1538-3598 ; 0254-9077 ; 0002-9955 ; 0098-7484
    ISSN (online) 1538-3598
    ISSN 0254-9077 ; 0002-9955 ; 0098-7484
    DOI 10.1001/jama.2023.19574
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Association Between Sublingual Buprenorphine-Naloxone Exposure and Dental Disease.

    Etminan, Mahyar / Rezaeianzadeh, Ramin / Kezouh, Abbas / Aminzadeh, Kevin

    JAMA

    2022  Volume 328, Issue 22, Page(s) 2269–2271

    MeSH term(s) Humans ; Administration, Sublingual ; Analgesics, Opioid/administration & dosage ; Analgesics, Opioid/adverse effects ; Analgesics, Opioid/therapeutic use ; Buprenorphine, Naloxone Drug Combination/administration & dosage ; Buprenorphine, Naloxone Drug Combination/adverse effects ; Buprenorphine, Naloxone Drug Combination/therapeutic use ; Narcotic Antagonists/administration & dosage ; Narcotic Antagonists/adverse effects ; Narcotic Antagonists/therapeutic use ; Opioid-Related Disorders/drug therapy ; Stomatognathic Diseases/chemically induced
    Chemical Substances Analgesics, Opioid ; Buprenorphine, Naloxone Drug Combination ; Narcotic Antagonists
    Language English
    Publishing date 2022-12-13
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2958-0
    ISSN 1538-3598 ; 0254-9077 ; 0002-9955 ; 0098-7484
    ISSN (online) 1538-3598
    ISSN 0254-9077 ; 0002-9955 ; 0098-7484
    DOI 10.1001/jama.2022.17485
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Risk of maculopathy with pentosan polysulfate sodium use.

    Bae, Steven S / Sodhi, Mohit / Maberley, David / Kezouh, Abbas / Etminan, Mahyar

    British journal of clinical pharmacology

    2022  Volume 88, Issue 7, Page(s) 3428–3433

    Abstract: Aims: Recent epidemiologic studies have examined the risk of maculopathy with pentosan polysulfate sodium (PPS), a drug indicated for the treatment of interstitial cystitis. However, results have been contradictory. Thus, we quantified the risk of ... ...

    Abstract Aims: Recent epidemiologic studies have examined the risk of maculopathy with pentosan polysulfate sodium (PPS), a drug indicated for the treatment of interstitial cystitis. However, results have been contradictory. Thus, we quantified the risk of maculopathy with PPS with a focus on risk with duration of use.
    Methods: We used a new user, retrospective cohort study with an active comparator. We created a cohort of mutually exclusive 6221 PPS users and 89 744 amitriptyline users, a tricyclic antidepressant also used for the treatment of pain secondary to interstitial cystitis. Subjects were selected from the PharMetrics Plus database (IQVIA, Durham, NC) from 2006 to 2020. Cohort members were followed to the first event of the study outcome (maculopathy) or end of enrolment. A Cox regression model was constructed to adjust for potential confounders.
    Results: The mean follow-up was 3.0 years for PPS users and amitriptyline users. The adjusted hazard ratio (HR) for maculopathy in PPS users was 2.64 (95% confidence interval [CI]: 1.90-3.68). The HR for the sensitivity analysis that combined maculopathy and age-related macular degeneration (AMD) was 1.38 (95% CI: 1.16-1.65). A cumulative duration-response pattern was observed, with use greater than 3 years having a 9.5-fold risk of maculopathy (HR = 9.56, 95% CI: 3.60-25.37) compared to a 2.3-fold risk of maculopathy with use for 1 year or less (HR = 2.27, 95% CI: 1.50-3.43). The number needed to harm for the first 4 years of use was 250.
    Conclusions: The results of this study suggest an increased risk of maculopathy with PPS use, particularly with longer duration of use.
    MeSH term(s) Amitriptyline/adverse effects ; Cystitis, Interstitial/chemically induced ; Cystitis, Interstitial/drug therapy ; Cystitis, Interstitial/epidemiology ; Humans ; Macular Degeneration/chemically induced ; Macular Degeneration/drug therapy ; Macular Degeneration/epidemiology ; Pentosan Sulfuric Polyester/adverse effects ; Retrospective Studies
    Chemical Substances Amitriptyline (1806D8D52K) ; Pentosan Sulfuric Polyester (37300-21-3)
    Language English
    Publishing date 2022-03-22
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 188974-6
    ISSN 1365-2125 ; 0306-5251 ; 0264-3774
    ISSN (online) 1365-2125
    ISSN 0306-5251 ; 0264-3774
    DOI 10.1111/bcp.15303
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: The Incidence of Sympathetic Ophthalmia After Trauma: A Meta-analysis.

    He, Bonnie / Tanya, Stuti M / Wang, Chao / Kezouh, Abbas / Torun, Nurhan / Ing, Edsel

    American journal of ophthalmology

    2021  Volume 234, Page(s) 117–125

    Abstract: Purpose: Sympathetic ophthalmia (SO) is a rare, bilateral panuveitis that occurs following open globe injury (OGI), with a variable incidence reported in the literature. Our objective was to determine the incidence proportion and incidence rate of SO ... ...

    Abstract Purpose: Sympathetic ophthalmia (SO) is a rare, bilateral panuveitis that occurs following open globe injury (OGI), with a variable incidence reported in the literature. Our objective was to determine the incidence proportion and incidence rate of SO following OGI to help guide shared physician-patient decision making.
    Design: Systematic review and meta-analysis.
    Methods: A systematic literature search was performed using the MEDLINE, EMBASE, and Cochrane databases from inception to November 2020 for population-based studies on OGI and SO in adults and children. Two reviewers independently screened search results. Random-effects meta-analyses were performed to calculate the incidence proportion and incidence rate. The Risk Of Bias In Non-Randomized Studies - of Interventions (ROBINS-I) tool was used to assess the risk of bias. The study was registered on PROSPERO CRD42020198920.
    Results: A total of 24 studies were utilized in the meta-analyses. After OGI, the estimated overall incidence proportion of SO was 0.19% (95% CI 0.14%-0.24%) and the incidence rate of SO was 33 per 100,000 person-years, (95% CI 19.61-56.64) with I
    Conclusions: SO after OGI is rare. The estimated incidence proportion and incidence rate are useful when counselling patients regarding management options after OGI. Further studies are needed to examine the influence of age, the extent and location of trauma, timing of repair, and prophylactic eye removal on the incidence of SO.
    MeSH term(s) Adult ; Child ; Eye Enucleation ; Eye Injuries/complications ; Eye Injuries/epidemiology ; Humans ; Incidence ; Ophthalmia, Sympathetic/diagnosis ; Ophthalmia, Sympathetic/epidemiology ; Ophthalmia, Sympathetic/etiology
    Language English
    Publishing date 2021-07-17
    Publishing country United States
    Document type Journal Article ; Meta-Analysis ; Review ; Systematic Review
    ZDB-ID 80030-2
    ISSN 1879-1891 ; 0002-9394
    ISSN (online) 1879-1891
    ISSN 0002-9394
    DOI 10.1016/j.ajo.2021.06.036
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Effects of hormonal contraceptives on dry eye disease: a population-based study.

    He, Bonnie / Iovieno, Alfonso / Etminan, Mahyar / Kezouh, Abbas / Yeung, Sonia N

    Eye (London, England)

    2021  Volume 36, Issue 3, Page(s) 634–638

    Abstract: Background: Hormonal contraceptives (HCs) are a known risk factor for dry eye disease (DED), yet the relationship between HCs use and DED in women of child-bearing age remains debatable. The aim of this study was to determine the association between HCs ...

    Abstract Background: Hormonal contraceptives (HCs) are a known risk factor for dry eye disease (DED), yet the relationship between HCs use and DED in women of child-bearing age remains debatable. The aim of this study was to determine the association between HCs and DED in females of reproductive age.
    Methods: This was a retrospective cohort study using data from IQVIA's electronic medical record (IQVIA, USA). 4,871,504 women (age 15-45) between 2008 and 2018 were followed to the first diagnosis of DED as defined by an ICD-9/10 code. DED cases also required at least two prescriptions of cyclosporine or lifitegrast topical drops within 60 days of the first code. The date of the first code was designated as the index date. Regular HCs users needed to have at least two prescriptions in both the first year and second year prior to the index date. For each case, five controls were selected and matched to cases by age and follow-up time. A conditional logistic regression model was used to adjust for confounders of DED and to calculate odds ratios (ORs).
    Results: HCs users were at a higher risk for DED than non-users. Regular users of HCs were more likely to develop DED (ORs = 2.73, 95% CI [2.21-3.73]) than irregular users. Those who used a greater number of HCs were at a higher risk for DED.
    Conclusions: This study indicates an increased risk of DED with HCs use in women of child-bearing age.
    MeSH term(s) Adolescent ; Adult ; Contraceptive Agents ; Dry Eye Syndromes/chemically induced ; Dry Eye Syndromes/diagnosis ; Dry Eye Syndromes/epidemiology ; Female ; Humans ; Male ; Middle Aged ; Odds Ratio ; Retrospective Studies ; Risk Factors ; Young Adult
    Chemical Substances Contraceptive Agents
    Language English
    Publishing date 2021-04-06
    Publishing country England
    Document type Journal Article
    ZDB-ID 91001-6
    ISSN 1476-5454 ; 0950-222X
    ISSN (online) 1476-5454
    ISSN 0950-222X
    DOI 10.1038/s41433-021-01517-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: The association between hormonal contraceptive use and glaucoma in women of reproductive age.

    Hogden, Kate / Mikelberg, Frederick / Sodhi, Mohit / Khosrow-Khavar, Farzin / Mansournia, Mohammad Ali / Kezouh, Abbas / Etminan, Mahyar

    British journal of clinical pharmacology

    2021  Volume 87, Issue 12, Page(s) 4780–4785

    Abstract: Aims: We aimed to investigate the association between hormonal contraceptive (HC) use and the incidence of glaucoma in females of reproductive age with a focus on duration and type of HCs used.: Methods: A retrospective cohort study with a case- ... ...

    Abstract Aims: We aimed to investigate the association between hormonal contraceptive (HC) use and the incidence of glaucoma in females of reproductive age with a focus on duration and type of HCs used.
    Methods: A retrospective cohort study with a case-control analysis (nested case-control) was undertaken using data from IQVIA's electronic medical record (IQVIA, USA) from 2008 to 2018. Within a cohort of 4 871 504 women, cases of glaucoma or ocular hypertension were identified. Subjects were followed to the first diagnosis of glaucoma. Each glaucoma case was matched to four controls by age, body mass index and follow up time. The main outcome measure was the first diagnosis of glaucoma defined by the first ICD-9/10 code for glaucoma or ocular hypertension.
    Results: Among 4 871 504 women identified, there were 2366 cases of glaucoma and 9464 controls. Regular users of hormonal contraceptives had an elevated risk of glaucoma compared to non-users with an adjusted incident rate ratio (aIRR) of 1.57 (95% CI: 1.29-1.92). Current users were of greatest risk (aIRR of 2.38, 95% CI: 1.81-3.13), whereas the aIRR among past users was 1.08 (95% CI: 0.82-1.43). The aIRR for glaucoma increased from 0.82 (95% CI: 0.70-0.95) among those with one or two prescriptions in the 2 years prior to the first diagnosis of glaucoma to 1.54 (95% CI: 1.32-1.81) among those with greater than four prescriptions.
    Conclusions: This nested case-control study demonstrated an elevated risk, albeit low, of glaucoma in females of reproductive age who use regular hormonal contraception. Future studies are needed to confirm these findings.
    MeSH term(s) Case-Control Studies ; Cohort Studies ; Contraceptives, Oral, Hormonal/adverse effects ; Female ; Glaucoma/chemically induced ; Glaucoma/diagnosis ; Glaucoma/epidemiology ; Humans ; Retrospective Studies
    Chemical Substances Contraceptives, Oral, Hormonal
    Language English
    Publishing date 2021-06-22
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 188974-6
    ISSN 1365-2125 ; 0306-5251 ; 0264-3774
    ISSN (online) 1365-2125
    ISSN 0306-5251 ; 0264-3774
    DOI 10.1111/bcp.14920
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  7. Article ; Online: Acetylcholinesterase inhibitors and risk of bleeding and acute ischemic events in non-hypertensive Alzheimer's patients.

    Al-Hamed, Faez Saleh / Kouniaris, Stamatis / Tamimi, Iskandar / Lordkipanidzé, Marie / Madathil, Sreenath Arekunnath / Kezouh, Abbas / Karp, Igor / Nicolau, Belinda / Tamimi, Faleh

    Alzheimer's & dementia (New York, N. Y.)

    2021  Volume 7, Issue 1, Page(s) e12184

    Abstract: 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 ... ...

    Abstract 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.
    Language English
    Publishing date 2021-08-20
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2832891-7
    ISSN 2352-8737 ; 2352-8737
    ISSN (online) 2352-8737
    ISSN 2352-8737
    DOI 10.1002/trc2.12184
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  8. Article ; Online: Oral Fluoroquinolones and Risk of Mitral and Aortic Regurgitation.

    Etminan, Mahyar / Sodhi, Mohit / Ganjizadeh-Zavareh, Saeed / Carleton, Bruce / Kezouh, Abbas / Brophy, James M

    Journal of the American College of Cardiology

    2019  Volume 74, Issue 11, Page(s) 1444–1450

    Abstract: Background: Recent studies have linked fluoroquinolones (FQs) to cardiac adverse events, including aortic dissection and aneurysm. To date, whether FQs can increase the risk of aortic or mitral regurgitation has not been studied.: Objectives: This ... ...

    Abstract Background: Recent studies have linked fluoroquinolones (FQs) to cardiac adverse events, including aortic dissection and aneurysm. To date, whether FQs can increase the risk of aortic or mitral regurgitation has not been studied.
    Objectives: This disproportionality analysis and case-control study examined whether FQs increase the risk of aortic and mitral regurgitation.
    Methods: Data from the U.S. Food and Drug Administration's adverse reporting system database was used to undertake a disproportionality analysis, and a random sample of 9,053,240 patients from the U.S. PharMetrics Plus database (IQVIA) was used for the matched nested case-control study. Current FQ exposure implied an active prescription at the index date or 30 days prior to the event date. Recent FQ exposure was defined as FQ use within days 31 to 60 and past within days 61 to 365 prior to the event date. Rate ratios (RRs) were compared to users of amoxicillin and azithromycin. Conditional logistic regression was used to compute RRs adjusting for confounders.
    Results: The reported odds ratio for the disproportionality analysis was 1.45 (95% confidence interval [CI]: 1.20 to 1.77). A total of 12,505 cases and 125,020 control subjects were identified in the case-control study. The adjusted RRs for current users of FQ compared with amoxicillin and azithromycin users were 2.40 (95% CI: 1.82 to 3.16) and 1.75 (95% CI: 1.34 to 2.29), respectively. The adjusted RRs for recent and past FQ users when compared with amoxicillin were 1.47 (95% CI: 1.03 to 2.09) and 1.06 (95% CI: 0.91 to 1.21), respectively.
    Conclusions: These results show that the risk of aortic and mitral regurgitation is highest with current use followed by recent use. No risk was observed with past use of FQs. Future studies are necessary to confirm or refute these associations.
    MeSH term(s) Administration, Oral ; Aged ; Aortic Valve Insufficiency/chemically induced ; Case-Control Studies ; Cross-Sectional Studies ; Female ; Fluoroquinolones/administration & dosage ; Fluoroquinolones/adverse effects ; Humans ; Male ; Middle Aged ; Mitral Valve Insufficiency/chemically induced ; Risk Assessment
    Chemical Substances Fluoroquinolones
    Language English
    Publishing date 2019-11-13
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 605507-2
    ISSN 1558-3597 ; 0735-1097
    ISSN (online) 1558-3597
    ISSN 0735-1097
    DOI 10.1016/j.jacc.2019.07.035
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  9. Article ; Online: Short and long-term barriers and facilitators of skin self-examination among individuals diagnosed with melanoma.

    Coroiu, Adina / Moran, Chelsea / Bergeron, Catherine / Drapeau, Martin / Wang, Beatrice / Kezouh, Abbas / Ernst, Jochen / Batist, Gerald / Körner, Annett

    BMC cancer

    2020  Volume 20, Issue 1, Page(s) 123

    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 ... ...

    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.
    MeSH term(s) Aged ; Early Detection of Cancer ; Female ; Humans ; Longitudinal Studies ; Male ; Melanoma/diagnosis ; Melanoma/epidemiology ; Middle Aged ; Neoplasm Staging ; Quebec/epidemiology ; Self Efficacy ; Self-Examination ; Severity of Illness Index ; Skin Neoplasms/diagnosis ; Skin Neoplasms/epidemiology
    Language English
    Publishing date 2020-02-14
    Publishing country England
    Document type Journal Article ; Observational Study
    ISSN 1471-2407
    ISSN (online) 1471-2407
    DOI 10.1186/s12885-019-6476-5
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  10. Article ; Online: Persistent Sexual Dysfunction with Finasteride 1 mg Taken for Hair Loss.

    Guo, Michael / Heran, Balraj / Flannigan, Ryan / Kezouh, Abbas / Etminan, Mahyar

    Pharmacotherapy

    2016  Volume 36, Issue 11, Page(s) 1180–1184

    Abstract: Purpose: To examine the risk of persistent sexual dysfunction (PSD) with finasteride 1 mg.: Methods: We conducted a retrospective cohort study using the IMS U.S. health claims database. From an original cohort of 6,110,723 patients, we identified ... ...

    Abstract Purpose: To examine the risk of persistent sexual dysfunction (PSD) with finasteride 1 mg.
    Methods: We conducted a retrospective cohort study using the IMS U.S. health claims database. From an original cohort of 6,110,723 patients, we identified 1390 men who had stopped using finasteride 1 mg and 20,000 randomly selected age- and calendar time-matched users of omeprazole from 2006 to 2014. First PSD event was defined as (1) the first PSD diagnosis through the first International Classification for Diseases, Ninth Revision, Clinical Modification) code for sexual dysfunction and (2) use of a phosphodiesterase inhibitor (sildenafil, tadalafil, or vardenafil).
    Results: In the primary analysis, we identified 1390 men taking finasteride 1 mg and 20,000 omeprazole users. The mean time to first PSD event after discontinuation of a finasteride 1 mg prescription was 391 days (SD, 357 days). The rate of PSD for finasteride 1 mg users and omeprazole users was 37.9 and 15.0 per 1000 person-years, respectively. For the primary analysis of sexual dysfunction, the adjusted hazard ratio (HR) comparing finasteride 1 mg users to omeprazole users was 1.62 (1.14-2.29). Adjusted HR in the secondary analysis comparing finasteride users to omeprazole users with respect to the first phosphodiesterase inhibitor was 2.73 (2.01-3.69).
    Conclusions: The risk of PSD in men who stopped finasteride 1 mg therapy was higher than that for omeprazole users. Patients who stopped finasteride therapy sought physician visits for sexual dysfunction up to 1 year after stopping finasteride.
    MeSH term(s) 5-alpha Reductase Inhibitors/administration & dosage ; 5-alpha Reductase Inhibitors/adverse effects ; Adult ; Alopecia/drug therapy ; Cohort Studies ; Finasteride/administration & dosage ; Finasteride/adverse effects ; Humans ; Middle Aged ; Omeprazole/administration & dosage ; Omeprazole/adverse effects ; Retrospective Studies ; Sexual Dysfunction, Physiological/chemically induced ; Sexual Dysfunction, Physiological/epidemiology ; Time Factors
    Chemical Substances 5-alpha Reductase Inhibitors ; Finasteride (57GNO57U7G) ; Omeprazole (KG60484QX9)
    Language English
    Publishing date 2016-10-20
    Publishing country United States
    Document type Comparative Study ; Journal Article
    ZDB-ID 603158-4
    ISSN 1875-9114 ; 0277-0008
    ISSN (online) 1875-9114
    ISSN 0277-0008
    DOI 10.1002/phar.1837
    Database MEDical Literature Analysis and Retrieval System OnLINE

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