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  1. Article ; Online: Writing letters to patients attending psychiatry clinics.

    Martin, Dave / Weetman, Katharine

    BMJ (Clinical research ed.)

    2023  Volume 383, Page(s) 2857

    MeSH term(s) Humans ; Ambulatory Care Facilities ; Writing ; Psychiatry
    Language English
    Publishing date 2023-12-04
    Publishing country England
    Document type Editorial
    ZDB-ID 1362901-3
    ISSN 1756-1833 ; 0959-8154 ; 0959-8146 ; 0959-8138 ; 0959-535X ; 1759-2151
    ISSN (online) 1756-1833
    ISSN 0959-8154 ; 0959-8146 ; 0959-8138 ; 0959-535X ; 1759-2151
    DOI 10.1136/bmj.p2857
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: The Estimated Lifetime Medical Cost of Diseases Attributable to Human Papillomavirus Infections Acquired in 2018.

    Chesson, Harrell W / Laprise, Jean-François / Brisson, Marc / Martin, Dave / Ekwueme, Donatus U / Markowitz, Lauri E

    Sexually transmitted diseases

    2021  Volume 48, Issue 4, Page(s) 278–284

    Abstract: Introduction: We estimated the lifetime medical costs of diagnosed cases of diseases attributable to human papillomavirus (HPV) infections acquired in 2018.: Methods: We adapted an existing mathematical model of HPV transmission and associated ... ...

    Abstract Introduction: We estimated the lifetime medical costs of diagnosed cases of diseases attributable to human papillomavirus (HPV) infections acquired in 2018.
    Methods: We adapted an existing mathematical model of HPV transmission and associated diseases to estimate the lifetime number of diagnosed cases of disease (genital warts; cervical intraepithelial neoplasia; and cervical, vaginal, vulvar, penile, anal, and oropharyngeal cancers) attributable to HPV infections that were acquired in 2018. For each of these outcomes, we multiplied the estimated number of cases by the estimated lifetime medical cost per case obtained from previous studies. We estimated the costs of recurrent respiratory papillomatosis in a separate calculation. Future costs were discounted at 3% annually.
    Results: The estimated discounted lifetime medical cost of diseases attributable to HPV infections acquired in 2018 among people aged 15 to 59 years was $774 million (in 2019 US dollars), of which approximately half was accounted for by infections in those aged 15 to 24 years. Human papillomavirus infections in women accounted for approximately 90% of the lifetime number of diagnosed cases of disease and 70% of the lifetime cost attributable to HPV infections acquired in 2018 among those aged 15 to 59 years.
    Conclusions: We estimated the lifetime medical costs of diseases attributable to HPV infections acquired in 2018 to be $774 million. This estimate is lower than previous estimates, likely due to the impact of HPV vaccination. The lifetime cost of disease attributable to incident HPV infections is expected to decrease further over time as HPV vaccination coverage increases.
    MeSH term(s) Adolescent ; Adult ; Condylomata Acuminata/epidemiology ; Cost-Benefit Analysis ; Female ; Humans ; Middle Aged ; Oropharyngeal Neoplasms ; Papillomavirus Infections/epidemiology ; Papillomavirus Vaccines ; Uterine Cervical Neoplasms ; Young Adult ; Uterine Cervical Dysplasia
    Chemical Substances Papillomavirus Vaccines
    Language English
    Publishing date 2021-02-04
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 435191-5
    ISSN 1537-4521 ; 0148-5717
    ISSN (online) 1537-4521
    ISSN 0148-5717
    DOI 10.1097/OLQ.0000000000001379
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Perfected and strengthened through trials and suffering.

    Martin, Dave

    JAAPA : official journal of the American Academy of Physician Assistants

    2007  Volume 20, Issue 1, Page(s) 52–53

    MeSH term(s) Emergency Medical Services ; Family Practice ; Homicide/psychology ; Humans ; Physician Assistants/psychology ; Rural Population ; Stress Disorders, Post-Traumatic/psychology ; Wounds, Gunshot/psychology ; Wounds, Gunshot/therapy
    Language English
    Publishing date 2007-01-16
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2415226-2
    ISSN 0893-7400 ; 1547-1896
    ISSN (online) 0893-7400
    ISSN 1547-1896
    DOI 10.1097/01720610-200701000-00011
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Selecting Counterions to Improve Ionized Hydrophilic Drug Encapsulation in Polymeric Nanoparticles.

    Dimiou, Savvas / McCabe, James / Booth, Rebecca / Booth, Jonathan / Nidadavole, Kalyan / Svensson, Olof / Sparén, Anders / Lindfors, Lennart / Paraskevopoulou, Vasiliki / Mead, Heather / Coates, Lydia / Workman, David / Martin, Dave / Treacher, Kevin / Puri, Sanyogitta / Taylor, Lynne S / Yang, Bin

    Molecular pharmaceutics

    2023  Volume 20, Issue 2, Page(s) 1138–1155

    Abstract: Hydrophobic ion pairing (HIP) can successfully increase the drug loading and control the release kinetics of ionizable hydrophilic drugs, addressing challenges that prevent these molecules from reaching the clinic. Nevertheless, polymeric nanoparticle ( ... ...

    Abstract Hydrophobic ion pairing (HIP) can successfully increase the drug loading and control the release kinetics of ionizable hydrophilic drugs, addressing challenges that prevent these molecules from reaching the clinic. Nevertheless, polymeric nanoparticle (PNP) formulation development requires trial-and-error experimentation to meet the target product profile, which is laborious and costly. Herein, we design a preformulation framework (solid-state screening, computational approach, and solubility in PNP-forming emulsion) to understand counterion-drug-polymer interactions and accelerate the PNP formulation development for HIP systems. The HIP interactions between a small hydrophilic molecule, AZD2811, and counterions with different molecular structures were investigated. Cyclic counterions formed amorphous ion pairs with AZD2811; the 0.7 pamoic acid/1.0 AZD2811 complex had the highest glass transition temperature (
    MeSH term(s) Polymers/chemistry ; Naphthols/chemistry ; Nanoparticles/chemistry ; Solubility ; Hydrophobic and Hydrophilic Interactions ; Drug Liberation
    Chemical Substances pamoic acid (7RRQ8QZ38N) ; Polymers ; Naphthols
    Language English
    Publishing date 2023-01-18
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2138405-8
    ISSN 1543-8392 ; 1543-8384
    ISSN (online) 1543-8392
    ISSN 1543-8384
    DOI 10.1021/acs.molpharmaceut.2c00855
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Optimal human papillomavirus vaccination strategies to prevent cervical cancer in low-income and middle-income countries in the context of limited resources: a mathematical modelling analysis.

    Drolet, Mélanie / Laprise, Jean-François / Martin, Dave / Jit, Mark / Bénard, Élodie / Gingras, Guillaume / Boily, Marie-Claude / Alary, Michel / Baussano, Iacopo / Hutubessy, Raymond / Brisson, Marc

    The Lancet. Infectious diseases

    2021  Volume 21, Issue 11, Page(s) 1598–1610

    Abstract: Background: Introduction of human papillomavirus (HPV) vaccination has been slow in low-income and middle-income countries (LMICs) because of resource constraints and worldwide shortage of vaccine supplies. To help inform WHO recommendations, we ... ...

    Abstract Background: Introduction of human papillomavirus (HPV) vaccination has been slow in low-income and middle-income countries (LMICs) because of resource constraints and worldwide shortage of vaccine supplies. To help inform WHO recommendations, we modelled various HPV vaccination strategies to examine the optimal use of limited vaccine supplies and best allocation of scarce resources in LMICs in the context of the WHO global call to eliminate cervical cancer as a public health problem.
    Methods: In this mathematical modelling analysis, we developed HPV-ADVISE LMIC, a transmission-dynamic model of HPV infection and diseases calibrated to four LMICs: India, Vietnam, Uganda, and Nigeria. For different vaccination strategies that encompassed use of a nine-valent vaccine (or a two-valent or four-valent vaccine assuming high cross-protection), we estimated three outcomes: reduction in the age-standardised rate of cervical cancer, number of doses needed to prevent one case of cervical cancer (NNV; as a measure of efficiency), and the incremental cost-effectiveness ratio (ICER; in 2017 international $ per disability-adjusted life-year [DALY] averted). We examined different vaccination strategies by varying the ages of routine HPV vaccination and number of age cohorts vaccinated, the population targeted, and the number of doses used. In our base case, we assumed 100% lifetime protection against HPV-16, HPV-18, HPV-31, HPV-33, HPV-45, HPV-52, and HPV-58; vaccination coverage of 80%; and a time horizon of 100 years. For the cost-effectiveness analysis, we used a 3% discount rate. Elimination of cervical cancer was defined as an age-standardised incidence of less than four cases per 100 000 woman-years.
    Findings: We predicted that HPV vaccination could lead to cervical cancer elimination in Vietnam, India, and Nigeria, but not in Uganda. Compared with no vaccination, strategies that involved vaccinating girls aged 9-14 years with two doses were predicted to be the most efficient and cost-effective in all four LMICs. NNV ranged from 78 to 381 and ICER ranged from $28 per DALY averted to $1406 per DALY averted depending on the country. The most efficient and cost-effective strategies were routine vaccination of girls aged 14 years, with or without a later switch to routine vaccination of girls aged 9 years, and routine vaccination of girls aged 9 years with a 5-year extended interval between doses and a catch-up programme at age 14 years. Vaccinating boys (aged 9-14 years) or women aged 18 years or older resulted in substantially higher NNVs and ICERs.
    Interpretation: We identified two strategies that could maximise efforts to prevent cervical cancer in LMICs given constraints on vaccine supplies and costs and that would allow a maximum of LMICs to introduce HPV vaccination.
    Funding: World Health Organization, Canadian Institute of Health Research, Fonds de recherche du Québec-Santé, Compute Canada, PATH, and The Bill & Melinda Gates Foundation.
    Translations: For the French and Spanish translations of the abstract see Supplementary Materials section.
    MeSH term(s) Adolescent ; Adult ; Child ; Cost-Benefit Analysis ; Developing Countries ; Female ; Humans ; Immunization Schedule ; Male ; Models, Biological ; Papillomavirus Infections/prevention & control ; Papillomavirus Vaccines/administration & dosage ; Papillomavirus Vaccines/economics ; Papillomavirus Vaccines/immunology ; Quality-Adjusted Life Years ; Uterine Cervical Neoplasms/prevention & control ; Vaccination ; Young Adult
    Chemical Substances Papillomavirus Vaccines
    Language English
    Publishing date 2021-07-07
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2061641-7
    ISSN 1474-4457 ; 1473-3099
    ISSN (online) 1474-4457
    ISSN 1473-3099
    DOI 10.1016/S1473-3099(20)30860-4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Effectiveness and Cost-Effectiveness of Human Papillomavirus Vaccination Through Age 45 Years in the United States.

    Laprise, Jean-François / Chesson, Harrell W / Markowitz, Lauri E / Drolet, Mélanie / Martin, Dave / Bénard, Élodie / Brisson, Marc

    Annals of internal medicine

    2019  Volume 172, Issue 1, Page(s) 22–29

    Abstract: Background: In the United States, the routine age for human papillomavirus (HPV) vaccination is 11 to 12 years, with catch-up vaccination through age 26 years for women and 21 years for men. U.S. vaccination policy on use of the 9-valent HPV vaccine in ... ...

    Abstract Background: In the United States, the routine age for human papillomavirus (HPV) vaccination is 11 to 12 years, with catch-up vaccination through age 26 years for women and 21 years for men. U.S. vaccination policy on use of the 9-valent HPV vaccine in adult women and men is being reviewed.
    Objective: To evaluate the added population-level effectiveness and cost-effectiveness of extending the current U.S. HPV vaccination program to women aged 27 to 45 years and men aged 22 to 45 years.
    Design: The analysis used HPV-ADVISE (Agent-based Dynamic model for VaccInation and Screening Evaluation), an individual-based transmission dynamic model of HPV infection and associated diseases, calibrated to age-specific U.S. data.
    Data sources: Published data.
    Target population: Women aged 27 to 45 years and men aged 22 to 45 years in the United States.
    Time horizon: 100 years.
    Perspective: Health care sector.
    Intervention: 9-valent HPV vaccination.
    Outcome measures: HPV-associated outcomes prevented and cost-effectiveness ratios.
    Results of base-case analysis: The model predicts that the current U.S. HPV vaccination program will reduce the number of diagnoses of anogenital warts and cervical intraepithelial neoplasia of grade 2 or 3 and cases of cervical cancer and noncervical HPV-associated cancer by 82%, 80%, 59%, and 39%, respectively, over 100 years and is cost saving (vs. no vaccination). In contrast, extending vaccination to women and men aged 45 years is predicted to reduce these outcomes by an additional 0.4, 0.4, 0.2, and 0.2 percentage points, respectively. Vaccinating women and men up to age 30, 40, and 45 years is predicted to cost $830 000, $1 843 000, and $1 471 000, respectively, per quality-adjusted life-year gained (vs. current vaccination).
    Results of sensitivity analysis: Results were most sensitive to assumptions about natural immunity and progression rates after infection, historical vaccination coverage, and vaccine efficacy.
    Limitation: Uncertainty about the proportion of HPV-associated disease due to infections after age 26 years and about the level of herd effects from the current HPV vaccination program.
    Conclusion: The current HPV vaccination program is predicted to be cost saving. Extending vaccination to older ages is predicted to produce small additional health benefits and result in substantially higher incremental cost-effectiveness ratios than the current recommendation.
    Primary funding source: Centers for Disease Control and Prevention.
    MeSH term(s) Adult ; Age Factors ; Cost-Benefit Analysis ; Female ; Health Care Costs ; Humans ; Male ; Middle Aged ; Papillomavirus Infections/economics ; Papillomavirus Infections/prevention & control ; Papillomavirus Vaccines/economics ; Papillomavirus Vaccines/therapeutic use ; Treatment Outcome ; United States/epidemiology ; Young Adult
    Chemical Substances Papillomavirus Vaccines
    Language English
    Publishing date 2019-12-10
    Publishing country United States
    Document type Journal Article
    ZDB-ID 336-0
    ISSN 1539-3704 ; 0003-4819
    ISSN (online) 1539-3704
    ISSN 0003-4819
    DOI 10.7326/M19-1182
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: The Impact of Human Papillomavirus Catch-Up Vaccination in Australia: Implications for Introduction of Multiple Age Cohort Vaccination and Postvaccination Data Interpretation.

    Drolet, Mélanie / Laprise, Jean-François / Brotherton, Julia M L / Donovan, Basil / Fairley, Christopher K / Ali, Hammad / Bénard, Élodie / Martin, Dave / Brisson, Marc

    The Journal of infectious diseases

    2017  Volume 216, Issue 10, Page(s) 1205–1209

    Abstract: We used transmission-dynamic modeling to estimate the added effectiveness of vaccinating multiple cohorts of females (12-26 years) in Australia compared with the theoretical introduction of routine-only (12-13 years) vaccination. Our results suggest that ...

    Abstract We used transmission-dynamic modeling to estimate the added effectiveness of vaccinating multiple cohorts of females (12-26 years) in Australia compared with the theoretical introduction of routine-only (12-13 years) vaccination. Our results suggest that vaccinating multiple cohorts produced markedly faster direct/herd effects, and it added benefits that last for 20-70 years. Furthermore, the number needed to vaccinate to prevent 1 anogential warts (AGW) case or cervical cancer (CC) was similar for routine + catch-up (AGW = 9.9, CC = 678) and routine-only vaccination (AGW = 9.9, CC = 677), thus providing similar levels of efficiency per person vaccinated.
    MeSH term(s) Adolescent ; Adult ; Australia/epidemiology ; Child ; Condylomata Acuminata/epidemiology ; Condylomata Acuminata/etiology ; Condylomata Acuminata/prevention & control ; Female ; Humans ; Papillomaviridae/immunology ; Papillomavirus Infections/complications ; Papillomavirus Infections/epidemiology ; Papillomavirus Infections/prevention & control ; Papillomavirus Vaccines/immunology ; Population Surveillance ; Uterine Cervical Neoplasms/epidemiology ; Uterine Cervical Neoplasms/etiology ; Uterine Cervical Neoplasms/prevention & control ; Vaccination ; Young Adult
    Chemical Substances Papillomavirus Vaccines
    Language English
    Publishing date 2017-09-28
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 3019-3
    ISSN 1537-6613 ; 0022-1899
    ISSN (online) 1537-6613
    ISSN 0022-1899
    DOI 10.1093/infdis/jix476
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Book: Kenaf

    Martin, Dave

    an overview

    1995  

    Abstract: Describes the history and uses of the kenaf plant. Also discusses problems and strategies in the kenaf industry. ...

    Title variant Kenaf fact sheet
    Institution Rainforest Action Network
    Author's details written by Dave Martin
    Abstract Describes the history and uses of the kenaf plant. Also discusses problems and strategies in the kenaf industry.
    Keywords Kenaf. ; Kenaf industry
    Language English
    Publisher Rainforest Action Network
    Publishing place San Francisco, CA
    Document type Book
    Note Caption title.
    Database NAL-Catalogue (AGRICOLA)

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  9. Article: The brain tissue response to implanted silicon microelectrode arrays is increased when the device is tethered to the skull.

    Biran, Roy / Martin, Dave C / Tresco, Patrick A

    Journal of biomedical materials research. Part A

    2007  Volume 82, Issue 1, Page(s) 169–178

    Abstract: The influence of tethering silicon microelectrode arrays on the cortical brain tissue reaction was compared with that of untethered implants placed in the same location by identical means using immunoflourescent methods and cell type specific markers ... ...

    Abstract The influence of tethering silicon microelectrode arrays on the cortical brain tissue reaction was compared with that of untethered implants placed in the same location by identical means using immunoflourescent methods and cell type specific markers over indwelling periods of 1-4 weeks. Compared with untethered, freely floating implants, tethered microelectrodes elicited significantly greater reactivity to antibodies against ED1 and GFAP over time. Regardless of implantation method or indwelling time, retrieved microelectrodes contained a layer of attached macrophages identified by positive immunoreactivity against ED1. In the tethered condition and in cases where the tissue surrounding untethered implants had the highest levels of ED1+ and GFAP+ immunoreactivity, the neuronal markers for neurofilament 160 and NeuN were reduced. Although the precise mechanisms are unclear, the present study indicates that simply tethering silicon microelectrode arrays to the skull increases the cortical brain tissue response in the recording zone immediately surrounding the microelectrode array, which signals the importance of identifying this important variable when evaluating the tissue response of different device designs, and suggests that untethered or wireless devices may elicit less of a foreign body response.
    MeSH term(s) Animals ; Brain/cytology ; Brain/physiology ; Brain/surgery ; Cell Count ; Ectodysplasins/metabolism ; Electric Stimulation/instrumentation ; Electric Stimulation/methods ; Glial Fibrillary Acidic Protein/metabolism ; Immunohistochemistry ; Macrophages/cytology ; Male ; Materials Testing ; Microelectrodes ; Neurons/cytology ; Prostheses and Implants ; Rats ; Silicon
    Chemical Substances Ectodysplasins ; Glial Fibrillary Acidic Protein ; Silicon (Z4152N8IUI)
    Language English
    Publishing date 2007-07
    Publishing country United States
    Document type Comparative Study ; Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 2099989-6
    ISSN 1552-4965 ; 1549-3296 ; 0021-9304
    ISSN (online) 1552-4965
    ISSN 1549-3296 ; 0021-9304
    DOI 10.1002/jbm.a.31138
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: Distinguishing anhydrous and hydrous forms of an active pharmaceutical ingredient in a tablet formulation using solid-state NMR spectroscopy.

    Griffin, John M / Martin, Dave R / Brown, Steven P

    Angewandte Chemie (International ed. in English)

    2007  Volume 46, Issue 42, Page(s) 8036–8038

    MeSH term(s) Chemistry, Pharmaceutical ; Hydrogen Bonding ; Magnetic Resonance Spectroscopy/methods ; Magnetic Resonance Spectroscopy/standards ; Pharmaceutical Preparations/analysis ; Pharmaceutical Preparations/chemistry ; Reference Standards ; Sensitivity and Specificity ; Tablets ; Water/chemistry
    Chemical Substances Pharmaceutical Preparations ; Tablets ; Water (059QF0KO0R)
    Language English
    Publishing date 2007
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2011836-3
    ISSN 1521-3773 ; 1433-7851
    ISSN (online) 1521-3773
    ISSN 1433-7851
    DOI 10.1002/anie.200702582
    Database MEDical Literature Analysis and Retrieval System OnLINE

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