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Dive into the research topics where Shadi Doroudgar is active.

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Featured researches published by Shadi Doroudgar.


Substance Use & Misuse | 2017

Polypharmacy, Infectious Diseases, Sexual Behavior, and Psychophysical Health Among Anabolic Steroid-Using Homosexual and Heterosexual Gym Patrons in San Francisco's Castro District

Eric J. Ip; Michael A. Yadao; Bijal M. Shah; Shadi Doroudgar; Paul J. Perry; Michael J. Tenerowicz; Lindsay Newsom; Amber A. Mann; Hermine Mkrtchyan; Harrison G. Pope

ABSTRACT Background: Limited studies based in England and Australia reported misuse of anabolic-androgenic steroids (AAS) among homosexual men to enhance body image. Anecdotally, AAS are also being misused by homosexual men in the United States. Since many AAS and certain performance enhancing drugs (PEDs) are administered via injection, this poses a potential vector for the spread of infectious disease in an already at-risk population. Objectives: This study compared and contrasted homosexual and heterosexual male gym clients regarding use of AAS and PEDs, use of alcohol and illicit drugs, seroprevalence of infectious disease, engagement in risky injection practices and sexual behaviors, and presence of psychiatric conditions. Methods: Recruitment and data collection occurred outside four exercise gyms in the San Francisco Castro District area between October 25, 2014 and March 10, 2015. Two hundred and twenty homosexual men and 73 heterosexual men completed the 114-item cross-sectional survey. Results: Ten percent of homosexual men reported lifetime AAS use. Homosexual men had almost four times more sexual partners and were over 14 times more likely to knowingly have unprotected intercourse with a known HIV positive person than heterosexual men. In addition, a quarter of homosexual men who injected drugs admitted to sharing used syringes or needles with another person. Conclusions/Importance: The current study is the first to confirm AAS use among homosexual men in the United States. Homosexual men partook in high-risk sexual behaviors and injection practices which may place them at greater risks for contracting and spreading HIV and other infectious diseases.


The American Journal of Pharmaceutical Education | 2016

Motivations and Predictors of Cheating in Pharmacy School

Eric J. Ip; Kathy Nguyen; Bijal M. Shah; Shadi Doroudgar; Monica K. Bidwal

Objective. To assess the prevalence, methods, and motivations for didactic cheating among pharmacy students and to determine predictive factors for cheating in pharmacy colleges and schools. Methods. A 45-item cross-sectional survey was conducted at all four doctor of pharmacy programs in Northern California. For data analysis, t test, Fisher exact test, and logistic regression were used. Results. Overall, 11.8% of students admitted to cheating in pharmacy school. Primary motivations for cheating included fear of failure, procrastination, and stress. In multivariate analysis, the only predictor for cheating in pharmacy school was a history of cheating in undergraduate studies. Conclusion. Cheating occurs in pharmacy schools and is motivated by fear of failure, procrastination, and stress. A history of past cheating predicts pharmacy school cheating. The information presented may help programs better understand their student population and lead to a reassessment of ethical culture, testing procedures, and prevention programs.


Human & Experimental Toxicology | 2016

An 11-year retrospective review of venlafaxine ingestion in children from the California Poison Control System

Shadi Doroudgar; Paul J. Perry; Grant Lackey; Natalia G. Veselova; Hannah Mae Chuang; Timothy E. Albertson

Venlafaxine is commonly used in the United States for approved and non-Food and Drug Administration–approved indications in adults. It is used off-label to treat children for psychiatric diagnoses. The aim of the study was to describe venlafaxine toxicities in children and to identify the venlafaxine dose per weight that correlates with toxicities. An 11-year retrospective study of venlafaxine ingestion in children was performed using the California Poison Control System (CPCS) database. Data was extracted from phone calls received by CPCS clinicians and follow-up phone calls made to assess the patient’s progress in a health-care setting. Inclusion criteria were venlafaxine ingestion cases reported to CPCS between January 2001 and December 2011, children aged 20 years and under, venlafaxine as the only ingested substance, managed in a health-care facility, and followed to a known outcome. Two hundred sixty-two cases met the study criteria. Common presentations included gastrointestinal (14.9%), altered mental status (13.7%), and tachycardia (13.4%). The majority of the cases resulted in no effect (51.5%) or minor effect (19.9%). The average estimated dose per weight was 18.3 mg/kg in all patients and 64.5 mg/kg in those experiencing moderate-to-severe adverse effects. Seizures occurred in only 4 of the 262 cases at doses ranging from 1500 to 7500 mg. Although the estimated dose per weight exceeded 10 mg/kg for the majority of the cases, only 12 cases resulted in moderate or severe outcomes. The majority of venlafaxine ingestion cases in children resulted in either no clinical effects or minor clinical effects.


Journal of Forensic Sciences | 2015

The Effects of Dextromethorphan on Driving Performance and the Standardized Field Sobriety Test.

Paul J. Perry; Kristian Fredriksen; Stephanie Chew; Eric J. Ip; Ingrid C. Lopes; Shadi Doroudgar; Kelan L. Thomas

Dextromethorphan (DXM) is abused most commonly among adolescents as a recreational drug to generate a dissociative experience. The objective of the study was to assess driving with and without DXM ingestion. The effects of one‐time maximum daily doses of DXM 120 mg versus a guaifenesin 400 mg dose were compared among 40 healthy subjects using a crossover design. Subjects’ ability to drive was assessed by their performance in a driving simulator (STISIM® Drive driving simulator software) and by conducting a standardized field sobriety test (SFST) administered 1‐h postdrug administration. The one‐time dose of DXM 120 mg did not demonstrate driving impairment on the STISIM® Drive driving simulator or increase SFST failures compared to guaifenesin 400 mg. Doses greater than the currently recommended maximum daily dose of 120 mg are necessary to perturb driving behavior.


Accident Analysis & Prevention | 2016

Effects of valerian on subjective sedation, field sobriety testing and driving simulator performance

Kelan L. Thomas; Joanne Canedo; Paul J. Perry; Shadi Doroudgar; Ingrid C. Lopes; Hannah Mae Chuang; Kimberly Bohnert

INTRODUCTION The availability of herbal medicines over-the-counter (OTC) has increased the use of natural products for self-treatment. Valerian has been used to effectively treat generalized anxiety disorder and insomnia. Studies suggest that valerenic acid may increase gamma-aminobutyric acid (GABA) modulation in the brain. Benzodiazepines have a similar mechanism of action and have been linked to an increased risk of hospitalizations due to traffic accidents. Despite the risk of somnolence, the safety of driving while under the influence of valerian remains unknown. PURPOSE The purpose of the study was to determine the effects of a one-time valerian 1600mg dose on subjective sedation effects, standardized field sobriety testing (SFST) and driving simulator performance parameters. METHODS The study design was a randomized, placebo-controlled, double-blind, cross-over trial. For each session, participants received either a dose of valerian or placebo. The outcome measures included a simple visual reaction test (SVRT), subjective sleepiness scales, SFST performance scores, and driving simulator performance parameters. RESULTS There were no significant differences in the SVRT or sleepiness scales between placebo and valerian exposures, but the study may have been underpowered. SFST total and individual test failure rates were not significantly different between the two exposures. The driving simulator performance parameters were equivalent between the two exposure conditions. CONCLUSIONS A one-time valerian 1600mg dose, often used to treat insomnia, does not appear to impair driving simulator performance after acute ingestion.


The American Journal of Pharmaceutical Education | 2018

Gender-Based Differences Among Pharmacy Students Involved in Academically Dishonest Behavior

Eric J. Ip; Jai Pal; Shadi Doroudgar; Monica K. Bidwal; Bijal Shah-Manek

Objective. To determine whether differences based on gender exist among pharmacy students involved in cases of admitted cheating or other academic dishonesty and to assess perceptions of academic dishonesty. Methods. Two cohorts of second-year male and female pharmacy students from four Northern California pharmacy programs were invited to complete a 45-item cross-sectional survey. Descriptive statistics and Pearson’s chi-squared test were used for statistical analysis. Results. There were 330 surveys completed with a 59% response rate. No significant gender-based differences were found regarding admitted cheating in pharmacy school and in regards to participating in various forms of academically dishonest behavior. Female students were more likely than male students to report witnessing a classmate copying another student’s assignment. Male students were less likely than female students to perceive a student who distributed a stolen exam as a cheater. Conclusion. No gender-based differences were noted in cases of admitted cheating or with regards to taking part in various forms of academically dishonest behavior. However, female students report witnessing cheating more than male students, and male students may have a more lenient perception toward academically dishonest behavior than female students. The information gathered from this study may provide further insight to pharmacy programs and educators regarding academic dishonesty at their institution.


Expert Opinion on Pharmacotherapy | 2018

What is the impact of the 2017 cochrane systematic review and meta-analysis that evaluated the use of PCSK9 inhibitors for lowering cardiovascular disease and mortality?

Mohamed A. Jalloh; Eric J. Ip; Shadi Doroudgar

ABSTRACT Introduction: In 2017, Schmidt et al. conducted a Cochrane systematic review and meta-analysis to evaluate the effect of using proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors to reduce low-density-lipoprotein- cholesterol (LDL-C) and cardiovascular disease (CVD). The Cochrane review was a systematic review and meta-analysis of 20 randomized, double-blinded trials that compared the use of PCSK9 inhibitors with statins/ezetimibe, ezetimibe, or placebo for a treatment duration of at least 24 weeks. The use of PCSK9 inhibitors lowered the risk for CVD (OR 0.86 (0.80 to 0.92)) but not mortality (OR 1.02 (0.91 to 1.14)) when compared to placebo. Areas covered: The following article evaluates the recently published Cochrane review and clarifies the efficacy of PCSK9 inhibitors for improving cardiovascular morbidity and mortality. Expert opinion: The Cochrane review discussed suggests that PCSK9 inhibitors are effective in lowering LDL-C and the risk of CVD but not the risk of mortality. The higher price of PCSK9 inhibitors is a further deterrent for using them as a substitute for statins – cholesterol lowering medications with history showing they lower mortality. Statins should remain the gold-standard cholesterol-lowering drug class until PCSK9 inhibitors become more affordable and demonstrate consistent efficacy for reducing CVD and mortality.


American Journal of Health-system Pharmacy | 2016

Factors influencing pursuit of postgraduate year 2 pharmacy residency training.

Sze Ngong Henry Lo; Jai Pal; Chia Shan Teoh; Jeffrey Shu; Chi Lun Pang; Melissa Lau; Helen Leung; Yamilette Mendez; Vanishree Rajagopalan; Shadi Doroudgar

Postgraduate year 1 (PGY1) and postgraduate year 2 (PGY2) pharmacy residency programs are critical for providing additional education and advanced training after completion of the doctor of pharmacy degree program. PGY1 programs generally have a broad practice focus, and PGY2 programs have a more


The Primary Care Companion To The Journal of Clinical Psychiatry | 2013

Evaluation of Trazodone and Quetiapine for Insomnia: An Observational Study in Psychiatric Inpatients

Shadi Doroudgar; Tony I. Chou; Junhua Yu; Karen Trinh; Jai Pal; Paul J. Perry


The American Journal of Pharmaceutical Education | 2018

Minority Trends and Barriers in Pharmacy School Enrollment

Nicholas Alonzo; Amrit Bains; Ga Rhee; Khin Htwe; Jamie Russell; Diana De Vore; Xia Li Chen; Michelle Nguyen; Vanishree Rajagopalan; Margaret Schulte; Shadi Doroudgar

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Paul J. Perry

Touro University California

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Eric J. Ip

Touro University California

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Kelan L. Thomas

Touro University California

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Hannah Mae Chuang

Touro University California

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Jai Pal

Touro University California

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Bijal M. Shah

Touro University California

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Ingrid C. Lopes

Touro University California

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Joanne Canedo

Touro University California

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Kimberly Bohnert

Touro University California

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Monica K. Bidwal

Touro University California

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