LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 10 of total 234

Search options

  1. Article ; Online: Investigating the ability to adhere to cardiometabolic medications with different properties: a retrospective cohort study of >500 000 patients in the USA.

    Lauffenburger, Julie C / Tesfaye, Helen / Solomon, Daniel H / Antman, Elliott M / Glynn, Robert J / Lee, Su Been / Tong, Angela / Choudhry, Niteesh K

    BMJ open

    2023  Volume 13, Issue 11, Page(s) e075840

    Abstract: Objective: Poor medication adherence remains highly prevalent and adversely affects health outcomes. Patients frequently describe properties of the pills themselves, like size and shape, as barriers, but this has not been evaluated objectively. We ... ...

    Abstract Objective: Poor medication adherence remains highly prevalent and adversely affects health outcomes. Patients frequently describe properties of the pills themselves, like size and shape, as barriers, but this has not been evaluated objectively. We sought to determine the extent to which oral medication properties thought to be influential translate into lower objectively-measured adherence.
    Design: Retrospective cohort study.
    Setting: US nationwide commercial claims database, 2016-2019.
    Participants: Among patients initiating first-line hypertension, diabetes or hyperlipidaemia treatment based on clinical guidelines, we measured pill size, shape, colour and flavouring, number of pills/day and fixed-dose combination status as properties.
    Outcome measures: Outcomes included discontinuation after the first fill (ie, never filling again over a minimum of 1-year follow-up) and long-term non-adherence (1-year proportion of days covered <0.80). We estimated associations between each property and outcomes, by therapeutic class (eg, statins), with multivariable logistic regression.
    Results: Across 604 323 patients, 14.6% discontinued after filling once (ie, were non-persistent), and 54.0% were non-adherent over 1-year follow-up. Large pill size was associated with non-adherence, except for thiazides (eg, metformin adjusted OR (aOR): 1.12, 95% CI: 1.06 to 1.18). Greater pill burden was associated with a higher risk of non-adherence across all classes (eg, metformin aOR: 1.58, 95% CI: 1.53 to 1.64 for two pills/day). Taking less than one pill/day was also associated with higher risk of non-adherence and non-persistence (eg, non-persistence statin aOR: 1.29, 95% CI: 1.20 to 1.38). Pill shape, colour, flavouring and combination status were associated with mixed effects across classes.
    Conclusions: Pill burden and pill size are key properties affecting adherence for almost all classes; others, like size and combination, could modestly affect medication adherence. Clinical interventions could screen patients for potential intolerance to medication and potentially implement more convenient dosing schedules.
    MeSH term(s) Humans ; United States ; Retrospective Studies ; Hypertension/drug therapy ; Hydroxymethylglutaryl-CoA Reductase Inhibitors/therapeutic use ; Medication Adherence ; Metformin/therapeutic use
    Chemical Substances Hydroxymethylglutaryl-CoA Reductase Inhibitors ; Metformin (9100L32L2N)
    Language English
    Publishing date 2023-11-10
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 2599832-8
    ISSN 2044-6055 ; 2044-6055
    ISSN (online) 2044-6055
    ISSN 2044-6055
    DOI 10.1136/bmjopen-2023-075840
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article ; Online: Exploring patient experiences coping with using multiple medications: a qualitative interview study.

    Lauffenburger, Julie C / Haff, Nancy / McDonnell, Marie E / Solomon, Daniel H / Antman, Elliott M / Glynn, Robert J / Choudhry, Niteesh K

    BMJ open

    2021  Volume 11, Issue 11, Page(s) e046860

    Abstract: Objective: Long-term adherence to evidence-based medications in cardiometabolic diseases remains poor, despite extensive efforts to develop and test interventions and deploy clinician performance incentives. The limited success of interventions may be ... ...

    Abstract Objective: Long-term adherence to evidence-based medications in cardiometabolic diseases remains poor, despite extensive efforts to develop and test interventions and deploy clinician performance incentives. The limited success of interventions may be due to ignored factors such as patients' experience of medication-taking. Despite being potentially addressable by clinicians, these factors have not been sufficiently explored, which is particularly important as patients use increasing numbers of medications. The aim is to explore patient perspectives on medication-taking, medication properties that are barriers to adherence, and coping strategies for their medication regimen.
    Design: Individual, in-person, semistructured qualitative interviews.
    Setting: Urban healthcare system.
    Participants: Twenty-six adults taking ≥2 oral medications for diabetes, hypertension or hyperlipidaemia with non-adherence. Interviews were digitally recorded and transcribed. Data were analysed using developed codes to generate themes. Representative quotations were selected to illustrate themes.
    Results: Participants' mean age was 55 years, 46% were female and 39% were non-white. Six key themes were identified: (1) medication-taking viewed as a highly inconvenient action (that patients struggle to remember to do); (2) negative implications because of inconvenience or illness perceptions; (3) actual medication regimens can deviate substantially from prescribed regimens; (4) certain medication properties (especially size and similar appearance with others) may contribute to adherence deviations; (5) development of numerous coping strategies to overcome barriers and (6) suggestions to make medication-taking easier (including reducing drug costs, simplifying regimen or dosing frequency and creating more palatable medications).
    Conclusion: Patients with poor adherence often find taking prescription medications to be undesirable and take them differently than prescribed in part due to properties of the medications themselves and coping strategies they have developed to overcome medication-taking challenges. Interventions that reduce the inconvenience of medication use and tailor medications to individual needs may be a welcome development.
    MeSH term(s) Adaptation, Psychological ; Adult ; Female ; Humans ; Medication Adherence ; Middle Aged ; Patient Outcome Assessment ; Prescription Drugs ; Qualitative Research
    Chemical Substances Prescription Drugs
    Language English
    Publishing date 2021-11-22
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 2599832-8
    ISSN 2044-6055 ; 2044-6055
    ISSN (online) 2044-6055
    ISSN 2044-6055
    DOI 10.1136/bmjopen-2020-046860
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article ; Online: Investigating the ability to adhere to cardiometabolic medications with different properties

    Daniel H Solomon / Robert J Glynn / Niteesh K Choudhry / Julie C Lauffenburger / Elliott M Antman / Su Been Lee / Helen Tesfaye / Angela Tong

    BMJ Open, Vol 13, Iss

    a retrospective cohort study of >500 000 patients in the USA

    2023  Volume 11

    Abstract: Objective Poor medication adherence remains highly prevalent and adversely affects health outcomes. Patients frequently describe properties of the pills themselves, like size and shape, as barriers, but this has not been evaluated objectively. We sought ... ...

    Abstract Objective Poor medication adherence remains highly prevalent and adversely affects health outcomes. Patients frequently describe properties of the pills themselves, like size and shape, as barriers, but this has not been evaluated objectively. We sought to determine the extent to which oral medication properties thought to be influential translate into lower objectively-measured adherence.Design Retrospective cohort study.Setting US nationwide commercial claims database, 2016–2019.Participants Among patients initiating first-line hypertension, diabetes or hyperlipidaemia treatment based on clinical guidelines, we measured pill size, shape, colour and flavouring, number of pills/day and fixed-dose combination status as properties.Outcome measures Outcomes included discontinuation after the first fill (ie, never filling again over a minimum of 1-year follow-up) and long-term non-adherence (1-year proportion of days covered <0.80). We estimated associations between each property and outcomes, by therapeutic class (eg, statins), with multivariable logistic regression.Results Across 604 323 patients, 14.6% discontinued after filling once (ie, were non-persistent), and 54.0% were non-adherent over 1-year follow-up. Large pill size was associated with non-adherence, except for thiazides (eg, metformin adjusted OR (aOR): 1.12, 95% CI: 1.06 to 1.18). Greater pill burden was associated with a higher risk of non-adherence across all classes (eg, metformin aOR: 1.58, 95% CI: 1.53 to 1.64 for two pills/day). Taking less than one pill/day was also associated with higher risk of non-adherence and non-persistence (eg, non-persistence statin aOR: 1.29, 95% CI: 1.20 to 1.38). Pill shape, colour, flavouring and combination status were associated with mixed effects across classes.Conclusions Pill burden and pill size are key properties affecting adherence for almost all classes; others, like size and combination, could modestly affect medication adherence. Clinical interventions could screen patients for potential intolerance to ...
    Keywords Medicine ; R
    Subject code 610
    Language English
    Publishing date 2023-11-01T00:00:00Z
    Publisher BMJ Publishing Group
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  4. Article: New biology and therapies in soft tissue sarcomas.

    Antman, K H

    Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie

    2003  Volume 55, Issue 9-10, Page(s) 553–557

    MeSH term(s) Chemotherapy, Adjuvant ; Gastrointestinal Neoplasms/etiology ; Gastrointestinal Neoplasms/genetics ; Gastrointestinal Neoplasms/pathology ; Gastrointestinal Neoplasms/therapy ; Humans ; Sarcoma/etiology ; Sarcoma/genetics ; Sarcoma/pathology ; Sarcoma/therapy ; Soft Tissue Neoplasms/etiology ; Soft Tissue Neoplasms/genetics ; Soft Tissue Neoplasms/pathology ; Soft Tissue Neoplasms/therapy
    Language English
    Publishing date 2003-03-07
    Publishing country France
    Document type Journal Article ; Review
    ZDB-ID 392415-4
    ISSN 1950-6007 ; 0753-3322 ; 0300-0893
    ISSN (online) 1950-6007
    ISSN 0753-3322 ; 0300-0893
    DOI 10.1016/s0753-3322(01)00127-5
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  5. Article: Overview of the six available randomized trials of high-dose chemotherapy with blood or marrow transplant in breast cancer.

    Antman, K H

    Journal of the National Cancer Institute. Monographs

    2001  , Issue 30, Page(s) 114–116

    MeSH term(s) Blood Transfusion/statistics & numerical data ; Bone Marrow Transplantation/statistics & numerical data ; Breast Neoplasms/drug therapy ; Breast Neoplasms/therapy ; Chemotherapy, Adjuvant/statistics & numerical data ; Humans ; Randomized Controlled Trials as Topic ; Survival Rate
    Language English
    Publishing date 2001
    Publishing country United States
    Document type Journal Article ; Meta-Analysis
    ISSN 1052-6773
    ISSN 1052-6773
    DOI 10.1093/oxfordjournals.jncimonographs.a003447
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  6. Article: A critique of the eleven randomised trials of high-dose chemotherapy for breast cancer.

    Antman, K H

    European journal of cancer (Oxford, England : 1990)

    2001  Volume 37, Issue 2, Page(s) 173–179

    Abstract: Data from 11 randomised studies on high-dose chemotherapy for breast cancer are currently available. Most investigators, patients and insurers would agree that the two discredited South African trials are uninterpretable, and that the Scandinavian trial ( ...

    Abstract Data from 11 randomised studies on high-dose chemotherapy for breast cancer are currently available. Most investigators, patients and insurers would agree that the two discredited South African trials are uninterpretable, and that the Scandinavian trial (which compares one very high-dose cycle versus six escalated dose cycles) does not ask the question of high-dose therapy versus conventional-dose therapy. Only two of the eight remaining studies randomised more than 200 patients (783 patients for the Cancer and Leukaemia Group B (CALGB) and 885 for the Dutch study). Both of these studies have trends in relapse-free survival favouring high-dose therapy. In a planned analysis of the first 284 patients entered into the Dutch study, with a median follow-up approximately 7 years, both disease-free and overall survival were significantly improved in the high-dose therapy arm. These and the other trials are discussed in detail below.
    MeSH term(s) Antineoplastic Agents/administration & dosage ; Breast Neoplasms/drug therapy ; Chemotherapy, Adjuvant/methods ; Disease-Free Survival ; Female ; Follow-Up Studies ; Humans ; Randomized Controlled Trials as Topic
    Chemical Substances Antineoplastic Agents
    Language English
    Publishing date 2001-01
    Publishing country England
    Document type Journal Article ; Meta-Analysis
    ZDB-ID 82061-1
    ISSN 1879-0852 ; 0959-8049 ; 0277-5379 ; 0964-1947
    ISSN (online) 1879-0852
    ISSN 0959-8049 ; 0277-5379 ; 0964-1947
    DOI 10.1016/s0959-8049(00)00347-6
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  7. Article: Introduction: the history of arsenic trioxide in cancer therapy.

    Antman, K H

    The oncologist

    2001  Volume 6 Suppl 2, Page(s) 1–2

    Abstract: Although arsenic can be poisonous, and chronic arsenic exposure from industrial or natural sources can cause serious toxicity, arsenic has been used therapeutically for more than 2,400 years. Thomas Fowler's potassium bicarbonate-based solution of ... ...

    Abstract Although arsenic can be poisonous, and chronic arsenic exposure from industrial or natural sources can cause serious toxicity, arsenic has been used therapeutically for more than 2,400 years. Thomas Fowler's potassium bicarbonate-based solution of arsenic trioxide (As(2)O(3)) was used empirically to treat a variety of disorders, and in 1878, was reported to reduce white blood cell counts in two normal individuals and one with "leucocythemia." Salvarsan, an organic arsenical for treating syphilis and trypanosomiasis, was developed in 1910 by Paul EHRLICH: In the 1930s, arsenic was reported to be effective in chronic myelogenous leukemia. After a decline in the use of arsenic during the mid-20th century, reports from China described a high proportion of hematologic responses in patients with acute promyelocytic leukemia (APL) who were treated with arsenic trioxide. Randomized clinical trials in the U.S. led to FDA approval of arsenic trioxide for relapsed or refractory APL in September 2000.
    MeSH term(s) Antineoplastic Agents/history ; Antineoplastic Agents/therapeutic use ; Arsenic Trioxide ; Arsenicals/history ; Arsenicals/therapeutic use ; History, 18th Century ; History, 19th Century ; History, 20th Century ; Humans ; Neoplasms/drug therapy ; Neoplasms/history ; Oxides/history ; Oxides/therapeutic use
    Chemical Substances Antineoplastic Agents ; Arsenicals ; Oxides ; Arsenic Trioxide (S7V92P67HO)
    Language English
    Publishing date 2001-04-05
    Publishing country United States
    Document type Historical Article ; Journal Article
    ZDB-ID 1409038-7
    ISSN 1083-7159
    ISSN 1083-7159
    DOI 10.1634/theoncologist.6-suppl_2-1
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  8. Article: Randomized trials of high dose chemotherapy for breast cancer.

    Antman, K H

    Biochimica et biophysica acta

    2001  Volume 1471, Issue 3, Page(s) M89–98

    Abstract: Now is not the end. It is not even the beginning of the end. But it is, perhaps, the end of the beginning'Winston Churchill in a speech to the Canadian Senate and House of Commons, December 30, 1941. In laboratory models of cancer, dose of cytotoxic ... ...

    Abstract 'Now is not the end. It is not even the beginning of the end. But it is, perhaps, the end of the beginning'Winston Churchill in a speech to the Canadian Senate and House of Commons, December 30, 1941. In laboratory models of cancer, dose of cytotoxic chemotherapy correlates with curative therapy, while cumulative dose is associated with longer survival for those who are not cured. These observations suggests a strategy of using high doses when cure is the objective but smaller doses over a prolonged period when palliation and survival are the goal. A strategy combining repetitive cycles of higher doses of cytotoxic therapy, followed by the optimal combination of hormonal and biological agents based on the tumor's receptors might contribute to both the highest possible cure rate and the longest survival. The development of bone marrow transplant (BMT) for leukemias, and its subsequent modification for support after high dose therapy for other malignancies, has a long, complex and emotional history in medicine. At least partly because of firmly held opinions and the way large randomized trials are funded in the United States, few American randomized trials of BMT or high dose therapy strategies have been completed. The vast majority of published randomized BMT and high dose studies are European. Interestingly, in contrast, two large American randomized trials of high dose chemotherapy for breast cancer had actually completed accrual. Accrual on a third was on target until the presentation of five very small or very early randomized trials at the American Society of Clinical Oncology meeting in May of 1999. Results from some of these trials, which were analyzed after a relatively brief follow-up, are too premature to allow definitive conclusions. Nevertheless, these data have been over and misinterpreted within the scientific and lay communities. The remaining studies included a limited number of patients, thus restricting the statistical power of the observations. The desire for quick answers impeded dispassionate analysis of the available data. The opportunity for collegial review of the data further deteriorated with another round of press coverage when the data from the South African adjuvant study were found to be unreliable. Rather than increasing commitment to accrual on randomized and appropriate pilot trials, accrual to the only large American study in existence at that time trickled to a halt. In response to press coverage, Susan Edmonds from the Fred Hutchinson Cancer Research Center observed that 'the NYT article tends to cast shadows generally on the therapy and those providing the therapy rather than pointing out early in the article (where the public will readily see it) that there are a number of very credible research institutions conducting research directed at breast cancer, some looking at high dose chemotherapy and stem cell transplantation.' Dr. Rodenhuis, presenting the large positive Dutch Randomized study (funded by the Dutch insurance industry) at ASCO in 2000, commented on the 'unreasonably high expectations until 1999' and 'unreasonably negative [opinion-ed] since 1999' for high dose adjuvant chemotherapy for breast cancer.
    MeSH term(s) Antineoplastic Combined Chemotherapy Protocols/administration & dosage ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; Breast Neoplasms/drug therapy ; Carboplatin/administration & dosage ; Clinical Trials, Phase II as Topic ; Cyclophosphamide/administration & dosage ; Doxorubicin/administration & dosage ; Drug Administration Schedule ; Epirubicin/administration & dosage ; Female ; Fluorouracil/administration & dosage ; Humans ; Methotrexate/administration & dosage ; Neoplasm Metastasis ; Randomized Controlled Trials as Topic ; Survival Analysis ; Thiotepa/administration & dosage
    Chemical Substances Epirubicin (3Z8479ZZ5X) ; Doxorubicin (80168379AG) ; Cyclophosphamide (8N3DW7272P) ; Thiotepa (905Z5W3GKH) ; Carboplatin (BG3F62OND5) ; Fluorouracil (U3P01618RT) ; Methotrexate (YL5FZ2Y5U1)
    Language English
    Publishing date 2001-03-06
    Publishing country Netherlands
    Document type Comparative Study ; Journal Article ; Review
    ZDB-ID 60-7
    ISSN 1879-2596 ; 1879-260X ; 1872-8006 ; 1879-2642 ; 1879-2618 ; 1879-2650 ; 0006-3002 ; 0005-2728 ; 0005-2736 ; 0304-4165 ; 0167-4838 ; 1388-1981 ; 0167-4889 ; 0167-4781 ; 0304-419X ; 1570-9639 ; 0925-4439 ; 1874-9399
    ISSN (online) 1879-2596 ; 1879-260X ; 1872-8006 ; 1879-2642 ; 1879-2618 ; 1879-2650
    ISSN 0006-3002 ; 0005-2728 ; 0005-2736 ; 0304-4165 ; 0167-4838 ; 1388-1981 ; 0167-4889 ; 0167-4781 ; 0304-419X ; 1570-9639 ; 0925-4439 ; 1874-9399
    DOI 10.1016/s0304-419x(00)00023-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  9. Article: High-dose chemotherapy in breast cancer: the end of the beginning?

    Antman, K H

    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation

    2000  Volume 6, Issue 5, Page(s) 469–475

    MeSH term(s) Antineoplastic Combined Chemotherapy Protocols/administration & dosage ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; Breast Neoplasms/drug therapy ; Breast Neoplasms/mortality ; Breast Neoplasms/pathology ; Clinical Trials as Topic ; Clinical Trials, Phase II as Topic ; Dose-Response Relationship, Drug ; Emotions ; Female ; France ; Health Policy ; Hematopoietic Stem Cell Transplantation ; Humans ; Netherlands ; Patient Selection ; Physicians/psychology ; Politics ; Public Opinion ; Randomized Controlled Trials as Topic ; Research Design ; Salvage Therapy ; Scandinavian and Nordic Countries ; South Africa ; Survival Analysis ; Treatment Outcome ; United States
    Language English
    Publishing date 2000-07-07
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 1474865-4
    ISSN 1083-8791
    ISSN 1083-8791
    DOI 10.1016/s1083-8791(00)70018-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  10. Article: Critique of the high-dose chemotherapy studies in breast cancer: a positive look at the data.

    Antman, K H

    Journal of clinical oncology : official journal of the American Society of Clinical Oncology

    1999  Volume 17, Issue 11 Suppl, Page(s) 30–34

    MeSH term(s) Antineoplastic Agents/administration & dosage ; Breast Neoplasms/drug therapy ; Breast Neoplasms/mortality ; Breast Neoplasms/therapy ; Dose-Response Relationship, Drug ; Female ; Humans ; Randomized Controlled Trials as Topic ; Research Design ; Scandinavian and Nordic Countries/epidemiology ; South Africa/epidemiology ; Survival Rate ; United States/epidemiology
    Chemical Substances Antineoplastic Agents
    Language English
    Publishing date 1999-11
    Publishing country United States
    Document type Comparative Study ; Journal Article ; Review
    ZDB-ID 604914-x
    ISSN 1527-7755 ; 0732-183X
    ISSN (online) 1527-7755
    ISSN 0732-183X
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

To top