Annette Regan

Dr. Annette Regan

orcid

Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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27 October 2011 in Tobacco Control
Verified
Journal Article
Closed access
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ARAnnette Regan
Annette Regan
GPGabbi Promoff
Gabbi Promoff
SDShanta R Dube
Shanta R Dube
RARene Arrazola
Rene Arrazola
Background Electronic nicotine delivery systems (ENDS), also referred to as electronic cigarettes or e-cigarettes, were introduced into the US market in 2007. Despite concerns regarding the long-term health impact of this product, there is little known about awareness and use of ENDS among adults in the USA. Methods A consumer-based mail-in survey (ConsumerStyles) was completed by 10 587 adults (≥18 years) in 2009 and 10 328 adults in 2010. Data from these surveys were used to monitor awareness, ever use and past month use of ENDS from 2009 to 2010 and to assess demographic characteristics and tobacco use of ENDS users. Results In this US sample, awareness of ENDS doubled from 16.4% in 2009 to 32.2% in 2010 and ever use more than quadrupled from 2009 (0.6%) to 2010 (2.7%). Ever use of ENDS was most common among women and those with lower education, although these were not the groups who had heard of ENDS most often. Current smokers and tobacco users were most likely to try ENDS. However, current smokers who had tried ENDS did not say they planned to quit smoking more often than smokers who had never tried them. Conclusions Given the large increase in awareness and ever use of ENDS during this 1-year period and the unknown impact of ENDS use on cigarette smoking behaviours and long-term health, continued monitoring of these products is needed.

1 December 2010 in American Journal of Public Health
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Journal Article
Closed access
ARAnnette Regan
Annette Regan
LMLela R. McKnight-Eily
Lela R. McKnight-Eily
SDShane P. Davis
Shane P. Davis
SDShanta R. Dube
Shanta R. Dube
Objectives. We estimated smoking prevalence, frequency, intensity, and cessation attempts among US adults with selected diagnosed lifetime mental illnesses. Methods. We used data from the 2007 National Health Interview Survey on 23 393 noninstitutionalized US adults to obtain age-adjusted estimates of smoking prevalence, frequency, intensity, and cessation attempts for adults screened as having serious psychological distress and persons self-reporting bipolar disorder, schizophrenia, attention deficit disorder or hyperactivity, dementia, or phobias or fears. Results. The age-adjusted smoking prevalence of adults with mental illness or serious psychological distress ranged from 34.3% (phobias or fears) to 59.1% (schizophrenia) compared with 18.3% of adults with no such illness. Smoking prevalence increased with the number of comorbid mental illnesses. Cessation attempts among persons with diagnosed mental illness or serious psychological distress were comparable to attempts among adults without mental illnesses or distress; however, lower quit ratios were observed among adults with these diagnoses, indicating lower success in quitting. Conclusions. The prevalence of current smoking was higher among persons with mental illnesses than among adults without mental illnesses. Our findings stress the need for prevention and cessation efforts targeting adults with mental illnesses.

3 October 2017 in BJOG: An International Journal of Obstetrics & Gynaecology
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Journal Article
Closed access
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EME Malacova
E Malacova
ARAnnette Regan
Annette Regan
Nashaat NassarNashaat Nassar
Nashaat Nassar
Camille Raynes-GreenowCamille Raynes-Greenow
Camille Raynes-Greenow
HLH Leonard
H Leonard
Gavin PereiraGavin Pereira
Gavin Pereira

1 June 2009 in Addictive Behaviors
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Journal Article
Closed access
ARAnnette Regan
Annette Regan
SDShanta R. Dube
Shanta R. Dube
TSTara W. Strine
Tara W. Strine
KKKurt Kroenke
Kurt Kroenke
RCRalph S. Caraballo
Ralph S. Caraballo
AMAli H. Mokdad
Ali H. Mokdad

13 November 2017 in The Annals of Family Medicine
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Journal Article
Open access
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ARAnnette Regan
Annette Regan
LBLauren Bloomfield
Lauren Bloomfield
IPIan Peters
Ian Peters
PEPaul V. Effler
Paul V. Effler
PURPOSE Seasonal influenza vaccine is recommended and funded for groups at higher risk of serious infection, but uptake is suboptimal. We conducted a randomized controlled trial of short message service (SMS) reminders for influenza vaccination. METHODS Six weeks after seasonal influenza vaccinations began, we identified high-risk patients who had a mobile telephone number on record at 10 practices in Western Australia. Thirty-two percent of the selected patients had already been vaccinated in the current year and were ineligible. Of the remaining 12,354 eligible patients at each practice one-half were randomly assigned to receive a vaccination reminder by SMS (intervention) and the rest received no SMS (control). Approximately 3 months after the SMS was sent (the study period), vaccination data were extracted from the patients’ electronic medical records. Log-binomial regression models were used to calculate the relative risk (RR) of vaccination between the intervention and control group. RESULTS Twelve-percent (769 of 6,177) of the intervention group and 9% (548 of 6,177) of the control group were vaccinated during the study period, a 39% relative increase attributable to the SMS (RR = 1.39; 95% CI, 1.26–1.54). For every 29 SMSs sent, costing $3.48, 1 additional high-risk patient was immunized. The greatest effect was observed for children younger than 5 years, whose parents were more than twice as likely to have their child vaccinated if they received a SMS reminder (RR = 2.43; 95% CI, 1.79–3.29). CONCLUSION We found SMS reminders to be a modestly effective, low-cost means to increase seasonal influenza vaccine coverage among high-risk patients.

31 December 2014 in Australian and New Zealand Journal of Obstetrics and Gynaecology
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Journal Article
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DMDonna B. Mak
Donna B. Mak
ARAnnette Regan
Annette Regan
SJSarah Joyce
Sarah Joyce
RGRobyn Gibbs
Robyn Gibbs
PEPaul V. Effler
Paul V. Effler