Clinic-wide, patient-level data were used from six academically-affiliated HIV medical clinics participating in a CDC and HRSA sponsored Retention in Care (RIC) intervention study, which has previously been described in detail.21 ,22 The six study sites include HIV clinics affiliated with Baylor College of Medicine, Houston, TX; Boston University Medical Center, Boston, MA; Johns Hopkins University, Baltimore, MD, State University of New York, Downstate Medical Center, Brooklyn, NY; University of Alabama at Birmingham, Birmingham, AL; and University of Miami, Miami, FL. The current study used systematically captured, de-identified, socio-demographic, clinical and medical visit patient-level data from a 2-year period preceding implementation of the intervention. The analysis included patients at the six study sites who had: (1) at least one scheduled primary HIV care appointment during the first 6 months (189 days) of a 12-month observation period (1 May 2008 – 30 April 2009) and (2) attended at least 1 primary HIV medical provider visit in the year preceding the observation period (1 May 2007 – 30 April 2008). These criteria were employed to identify established clinic patients in whom retention in care could be measured. The RIC research protocol received Institutional Review Board approval at all study sites.
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Retention in Care
Retention in Care
Retention in Care refers to the consistent engagement and active participation of individuals in their healthcare management over time.
This involves patients regularly attending scheduled appointments, adhering to treatment plans, and maintaining open communication with their healthcare providers.
Effective retention strategies are crucial for managing chronic conditions, improving health outcomes, and reducing the risk of disease progression or complications.
By optimizing retention in care, healthcare providers can enhance patients' quality of life, foster better treatment adherence, and ultimately, contribute to more successful long-term disease managment.
This involves patients regularly attending scheduled appointments, adhering to treatment plans, and maintaining open communication with their healthcare providers.
Effective retention strategies are crucial for managing chronic conditions, improving health outcomes, and reducing the risk of disease progression or complications.
By optimizing retention in care, healthcare providers can enhance patients' quality of life, foster better treatment adherence, and ultimately, contribute to more successful long-term disease managment.
Most cited protocols related to «Retention in Care»
Ethics Committees, Research
HIV-1
Patients
Pharmaceutical Preparations
Primary Health Care
Retention (Psychology)
Retention in Care
Communicable Diseases
Diagnosis
Disease, Chronic
Disease Progression
Early Therapy
HIV Infections
HIV Seropositivity
Patients
Retention in Care
Signs, Vital
Therapeutics
Transmission, Communicable Disease
CD4+ Cell Counts
Disease Progression
Gender
Opportunistic Infections
Patients
Retention in Care
Treatment Protocols
We used the Cost-Effectiveness of Preventing AIDS Complications (CEPAC)–Pediatric model to simulate a cohort of HIV-exposed infants in South Africa undergoing 2 EID algorithms: 6-week EID testing without confirmatory testing and 6-week EID testing with confirmatory testing. The CEPAC–Pediatric model is a first-order Monte Carlo simulation model of paediatric HIV infection, disease progression, diagnosis, and treatment [19 (link)–21 (link)]. For this analysis, we simulated HIV-exposed infants (born to women living with HIV) from birth through death. Risk of intrauterine or intrapartum HIV infection was modelled as a 1-time risk, based on 3 key maternal characteristics: the probability a mother was aware of her HIV diagnosis during pregnancy; the probability that she received ART during pregnancy, reflecting prevention of MTCT (PMTCT) coverage; and maternal CD4 count for women not receiving ART, reflecting disease stage. Uninfected infants faced a monthly risk of postpartum transmission based on these same characteristics until complete cessation of breastfeeding. All simulated patients faced monthly risks of non-HIV-related mortality. After HIV infection occurred, patients faced additional risks of opportunistic infections (OIs) and HIV-related mortality based on their age, CD4 percent (age < 5 years) or CD4 count (age ≥ 5 years), retention in care, and ART use. Full details of the CEPAC–Pediatric model structure are available in S1 Text and S2 Table and at http://web2.research.partners.org/cepac/model.html .
This work was approved by the Partners Human Research Committee, Boston, MA, US.
This work was approved by the Partners Human Research Committee, Boston, MA, US.
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Acquired Immunodeficiency Syndrome
CD4+ Cell Counts
Childbirth
Diagnosis
Disease Progression
HIV Infections
Homo sapiens
Infant
Mothers
Patients
Pregnancy
Retention in Care
Transmission, Communicable Disease
Woman
The design of MCH-ART is composed of 3 interrelated phases with observational and experimental elements, in which HIV-infected pregnant women are followed up during the antenatal and postnatal periods (Fig. 1 ). Throughout, participants attend study measurement visits conducted separately from routine ART service appointments.
Phase 1 is a cross-sectional evaluation of consecutively enrolled HIV-infected pregnant women seeking antenatal care. This phase of the study allows characterization of the health status of the population of HIV-infected pregnant women seeking care at the Gugulethu MOU and the services they receive. Phase 2 of the study is an observational cohort of all women in phase 1 who are eligible for initiation of ART (following local public sector guidelines), from their second antenatal clinic visit until their first postpartum clinic visit (conducted within 7 days postpartum). This phase of the study provides detailed description of ART initiation and antenatal follow-up in the population of women who will be involved in the postnatal component of the study.
Phase 3 of the study is a randomized trial of strategies for delivering ART to women during the postpartum period. Women enrolled in phase 2 who are breastfeeding their infants (regardless of infant HIV status) are approached to participate in the trial at the first routine postpartum clinic visit. Consenting eligible women are randomized to 1 of 2 approaches to providing ART:
The sample sizes for each phase are shown in Figure1 . An estimated 480 women are required in phase 3 to detect a 15% absolute difference in the combined endpoint of maternal viral suppression and retention in care through 12 months postpartum. To achieve this sample size, we anticipated enrolling up to 600 women in phase 2, and for this, a maximum of 1600 women were enrolled into phase 1. Ethical approval for the study, including the informed consent process, was provided by the Human Research Ethics Committee of the University of Cape Town, Faculty of Health Sciences and the Columbia University Medical Centre Institutional Review Board.
Phase 1 is a cross-sectional evaluation of consecutively enrolled HIV-infected pregnant women seeking antenatal care. This phase of the study allows characterization of the health status of the population of HIV-infected pregnant women seeking care at the Gugulethu MOU and the services they receive. Phase 2 of the study is an observational cohort of all women in phase 1 who are eligible for initiation of ART (following local public sector guidelines), from their second antenatal clinic visit until their first postpartum clinic visit (conducted within 7 days postpartum). This phase of the study provides detailed description of ART initiation and antenatal follow-up in the population of women who will be involved in the postnatal component of the study.
Phase 3 of the study is a randomized trial of strategies for delivering ART to women during the postpartum period. Women enrolled in phase 2 who are breastfeeding their infants (regardless of infant HIV status) are approached to participate in the trial at the first routine postpartum clinic visit. Consenting eligible women are randomized to 1 of 2 approaches to providing ART:
Referral to general adult ART services from approximately 4–8 weeks postpartum (the local standard of care), or,
Continued receipt of ART in the antenatal clinic, as part of an MCH-focused ART service that only refers women to general adult ART services after the end of breastfeeding.
The sample sizes for each phase are shown in Figure
Adult
Care, Prenatal
Clinic Visits
Ethics Committees, Research
Faculty
Homo sapiens
Infant
Population Health
Pregnant Women
Public Sector
Retention in Care
Woman
Most recents protocols related to «Retention in Care»
The extracted data from the ePMS was matched and merged with the patient data obtained from the PCBs using the unique ART numbers allocated (unique patient identifiers) at each ART clinic. A Microsoft Excel (Microsoft Corporation, Washington, DC, USA) spreadsheet was created from the merged data. The extracted anonymized data was saved into a password-protected excel file to prevent any unauthorized access or alterations of the data. The merged complete excel spreadsheet was imported into the SPSS statistical software (IBM SPSS version 28, IBM Corp. USA) for analysis. Descriptive statistics were carried out to describe the demographic and clinical characteristics of the adolescent participants included in the study, at baseline and during the following 36-month period. Bivariate analysis was executed utilizing the Chi-square test to determine the association, and the significance thereof, between retention in care and the demographic and clinical variables (age, sex, duration on ART, age at ART initiation, HIV disclosure status, WHO stage at ART initiation, current ART regimen, ART regimen at initiation, TB screening results, viral suppression status and healthcare facility level). Comparisons were performed between retention in care and demographic and clinical parameters at 6, 12, 18, 24 and 36 months post initiation on ART. Fisher’s exact test was used as an alternative to the Chi-square test in instances of sparse data (< 5 in any cell).
The Cox regression (Cox Proportional Hazards model) analysis was performed to adjust for potential confounders and interactions, to determine predictors for retention in care. The Cox proportional hazard model utilized the backward stepwise analysis, with the initial model inclusive of all candidate variables. The least significant variable was subsequently removed at each iteration until none of the nonsignificant variables remained. Variables were removed from the model at a set significance level of p < 0.05. The Complete Case Analysis (CCA) was used as less than 5% of the cases had missing data on all variables in the main analysis. Survival analysis was assessed with “Patient retention status at the end of the period” as the outcome of interest. A comparative survival analysis for the age and sex of the study participants using Kaplan-Meier survival curves was conducted [24 ]. Using Cox regression, factors influencing retention in care at months 6, 12, 18, 24 and 36 were established. Both the unadjusted and adjusted hazard ratios and their p-values were computed.
The Cox regression (Cox Proportional Hazards model) analysis was performed to adjust for potential confounders and interactions, to determine predictors for retention in care. The Cox proportional hazard model utilized the backward stepwise analysis, with the initial model inclusive of all candidate variables. The least significant variable was subsequently removed at each iteration until none of the nonsignificant variables remained. Variables were removed from the model at a set significance level of p < 0.05. The Complete Case Analysis (CCA) was used as less than 5% of the cases had missing data on all variables in the main analysis. Survival analysis was assessed with “Patient retention status at the end of the period” as the outcome of interest. A comparative survival analysis for the age and sex of the study participants using Kaplan-Meier survival curves was conducted [24 ]. Using Cox regression, factors influencing retention in care at months 6, 12, 18, 24 and 36 were established. Both the unadjusted and adjusted hazard ratios and their p-values were computed.
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Adolescent
Cells
Inclusion Bodies
Patients
Procarbazine
Retention (Psychology)
Retention in Care
Treatment Protocols
The primary outcome of this study was retention in HIV care. Longitudinal data were collected from routine clinic visits of all adolescents enrolled for ART in the Windhoek district. We considered ‘point’ retention at 6 months post-ART initiation, which can be defined as alive or the presence of individuals in ART services six months after initiating ART or any time thereafter [22 ]. We considered 36-month retention in care from January 2019 to December 2021, using six monthly intervals. The programmatic definition using the six months ‘point’ retention was preferred to align with recent guidance on multi-month prescription and multi-month dispensing of ART in Namibia [23 ]. The predictor variables extracted from the electronic database include age, sex, WHO stage at ART initiation, age at ART initiation, ART regimen at initiation, current ART regimen, duration on ART, TB screening results, HIV disclosure status, HIV viral load results and healthcare facility level.
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Adolescent
Retention (Psychology)
Retention in Care
Treatment Protocols
In this study, we defined retention in ART care as the proportion of the infected patients who are remaining alive and are still receiving health care at study facilities after they were initiated on therapy.2 ,9 (link) Patients were classified as not being on ART at the time they stopped treatment, as being lost to follow-up (LTFU), or as having died at the study facility
Patients
Retention in Care
Recruitment and retention of care homes, residents, and care-staff in both intervention and control conditions will be calculated to inform the number of care homes needed to achieve the target sample size for a future definitive trial. Acceptability, fidelity, and adherence to COG-D intervention protocol will be evaluated with completion rates for staff training and COG-D assessments, use and display of Daisies and revisions to care-plan based on COG-D assessments.
Feasibility of a Health Economic assessment will be explored in the ability to collect the data required (COG-D use, resource use, health and quality of life of residents) to undertake a cost-effectiveness analysis in the definitive trial and estimate potential costs and health benefits of the intervention.
Demographic data for residents (age, ethnicity, length of time in care home, gender, dementia diagnosis) will be collected from care plans. For staff, data will be obtained as part of the anonymous staff questionnaire (further training completed, duration of employment at care home) or in a short questionnaire preceding the staff training (role in care home, ethnicity (to explore diversity), age category, gender).
Candidate outcome measures for residents (by proxy) will be collected in interviews with researchers and staff outcomes are collected in the anonymous staff questionnaire (self-completed). Data completion rates of the candidate outcome measures (at each time point) will be calculated to determine which is the most appropriate primary outcome, agree other study measures and inform sample size calculation for the definitive trial.
Feasibility of a Health Economic assessment will be explored in the ability to collect the data required (COG-D use, resource use, health and quality of life of residents) to undertake a cost-effectiveness analysis in the definitive trial and estimate potential costs and health benefits of the intervention.
Demographic data for residents (age, ethnicity, length of time in care home, gender, dementia diagnosis) will be collected from care plans. For staff, data will be obtained as part of the anonymous staff questionnaire (further training completed, duration of employment at care home) or in a short questionnaire preceding the staff training (role in care home, ethnicity (to explore diversity), age category, gender).
Candidate outcome measures for residents (by proxy) will be collected in interviews with researchers and staff outcomes are collected in the anonymous staff questionnaire (self-completed). Data completion rates of the candidate outcome measures (at each time point) will be calculated to determine which is the most appropriate primary outcome, agree other study measures and inform sample size calculation for the definitive trial.
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Dementia
Diagnosis
Ethnicity
Gender
Infantile Neuroaxonal Dystrophy
Retention (Psychology)
Retention in Care
In-depth interviews will be conducted with 3 key stakeholder groups: patient supporters, study participants, and clinic leadership and public health officials. Interviews with patient supporters will occur before and 12 months after the implementation of mLAR to assess the nature of service delivery, client interactions and how this differs from standard linkage activities, barriers and facilitators of engaging out-of-care patients, challenges and solutions to the service delivery, and recommendations for service delivery improvements and expansion of reach. We will also conduct interviews with study participants randomized to the control or intervention arms. All participants will be asked about their experiences living with and engaging in HIV care, including facilitators and barriers to appointments and medication adherence, past experiences dropping out of care, impressions of HIV-related services they received, as well as recommendations for additional services. Participants randomized to the intervention arm will also be asked about their experience using the app, their satisfaction with features of the app such as the automated messaging they received, their motivation for engaging the patient supporter–delivered SMS text messages, their perception of the impact of app usage on their care, and their suggestions for other ways the mobile phone may facilitate HIV retention in care and adherence to medications. We will also assess facilitators and barriers to app use. Interviews with clinic leaders and public health officials will explore perceptions of the intervention’s integration into linkage and engagement of care activities at clinics or the health department, as well as recommendations for service delivery improvements. These interviews will provide insights about policy, acceptability, political buy-in for the intervention, and the potential for sustainability and adoption in other settings going forward.
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Motivation
Natural Childbirth
Obstetric Delivery
Patients
Retention in Care
Satisfaction
Top products related to «Retention in Care»
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More about "Retention in Care"
Retention in care is a critical aspect of healthcare management, ensuring consistent patient engagement and active participation in their treatment over time.
This involves regularly attending scheduled appointments, adhering to prescribed treatment plans, and maintaining open communication with healthcare providers.
Effective retention strategies are crucial for managing chronic conditions, improving health outcomes, and reducing the risk of disease progression or complications.
By optimizing retention in care, healthcare providers can enhance patients' quality of life, foster better treatment adherence, and contribute to more successful long-term disease management.
This is particularly important for conditions that require ongoing monitoring and management, such as diabetes, hypertension, and HIV/AIDS.
Retention in care is often measured using various statistical software, such as SAS 9.4, Stata version 13, Stata 12.0, STATA version 12, Stata 16, Stata, Stata/SE software version 13, and SPSS Statistics for Windows, Version 24.0.
These tools can help healthcare providers analyze patient data, identify patterns, and develop targeted interventions to improve retention rates.
Factors that can influence retention in care include patient demographics, socioeconomic status, comorbidities, transportation challenges, and the overall quality of the healthcare system.
Addressing these barriers through patient-centered approaches, such as providing transportation assistance, offering flexible appointment scheduling, and improving communication between patients and providers, can significantly enhance retention in care.
Additionally, the use of reduced glutathione, a naturally occurring antioxidant, has been studied for its potential to support overall health and well-being, which may positively impact patient engagement and retention in care.
Stata 11 is another statistical software that can be used to analyze the relationship between reduced glutathione and various health outcomes.
By understanding the importance of retention in care and utilizing the insights gained from statistical analysis, healthcare providers can develop and implement effective strategies to improve patient engagement, enhance treatment adherence, and ultimately, contribute to better long-term health outcomes.
This involves regularly attending scheduled appointments, adhering to prescribed treatment plans, and maintaining open communication with healthcare providers.
Effective retention strategies are crucial for managing chronic conditions, improving health outcomes, and reducing the risk of disease progression or complications.
By optimizing retention in care, healthcare providers can enhance patients' quality of life, foster better treatment adherence, and contribute to more successful long-term disease management.
This is particularly important for conditions that require ongoing monitoring and management, such as diabetes, hypertension, and HIV/AIDS.
Retention in care is often measured using various statistical software, such as SAS 9.4, Stata version 13, Stata 12.0, STATA version 12, Stata 16, Stata, Stata/SE software version 13, and SPSS Statistics for Windows, Version 24.0.
These tools can help healthcare providers analyze patient data, identify patterns, and develop targeted interventions to improve retention rates.
Factors that can influence retention in care include patient demographics, socioeconomic status, comorbidities, transportation challenges, and the overall quality of the healthcare system.
Addressing these barriers through patient-centered approaches, such as providing transportation assistance, offering flexible appointment scheduling, and improving communication between patients and providers, can significantly enhance retention in care.
Additionally, the use of reduced glutathione, a naturally occurring antioxidant, has been studied for its potential to support overall health and well-being, which may positively impact patient engagement and retention in care.
Stata 11 is another statistical software that can be used to analyze the relationship between reduced glutathione and various health outcomes.
By understanding the importance of retention in care and utilizing the insights gained from statistical analysis, healthcare providers can develop and implement effective strategies to improve patient engagement, enhance treatment adherence, and ultimately, contribute to better long-term health outcomes.