Publications by authors named "Safford M"

This nationwide cross-sectional study explored the relationship between ambulatory care fragmentation and medication use in older US adults, examining variations by chronic conditions and race. Utilizing data from the 2003-2016 REasons for Geographic and Racial Differences in Stroke (REGARDS) cohort study linked with fee-for-service Medicare claims, the authors analyzed care fragmentation (measured by the reversed Bice-Boxerman Index) and medication counts through a 2-week in-person prescription inventory. They employed negative binomial regression, adjusting for potential confounders, and conducted subgroup analyses based on chronic conditions and race.

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Background: Social determinants of health (SDOH) may influence 30-day readmission or emergency department (ED) use following acute myocardial infarction (AMI) hospitalizations. Understanding this relationship will promote the development of interventions and policies to reduce readmissions.

Objectives: The aim of the study was to test associations between SDOH and readmission after AMI.

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Background: We compared the atherosclerotic cardiovascular disease (ASCVD) risk prediction performance of the American Heart Association's Predicting Risk of Cardiovascular Disease Events (PREVENT) Base and PREVENT Full equations (includes urine albumin/creatinine ratio, glycated hemoglobin, and social deprivation index) with the pooled cohort equations (PCEs).

Methods: We included adults, aged 40 to 75 years, with no history of ASCVD, diabetes, or statin use in 2009 from Kaiser Permanente Southern California and followed up through 2019. ASCVD was defined as myocardial infarction, fatal coronary heart disease, and fatal and nonfatal ischemic stroke.

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Background: Black people are more likely to have hypertension and report lower quality of care than White people. Patient-provider race concordance could improve perceived quality of care, potentially lessening disparities.

Objective: Investigate the association between patient-provider race concordance and patient-perceived quality of chronic disease care, as measured by the Patient Assessment of Chronic Illness Care (PACIC) scale.

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Background: Inflammation plays a key role in the development of heart failure (HF), and diet is a known modifiable factor that modulates systemic inflammation. The dietary inflammatory score (DIS) is a tool that quantifies the inflammatory components of diet. We sought to determine whether the DIS is associated with incident HF events.

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Background: Increased burden of socially determined vulnerabilities (SDV), which include nonmedical conditions that contribute to patient health, is associated with incident heart failure (HF). Mediators of this association have not been examined. We aimed to determine if a healthy lifestyle mediates the association between SDV and HF.

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Background: Systemic sclerosis is a chronic and rare connective tissue disease with multiorgan effects, including interstitial lung disease (ILD). Navigating systemic sclerosis-interstitial lung disease presents a challenge for patients due to the gaps in patient education, which can impact patient health and quality of life. This study utilized the nominal group technique to identify priority knowledge gaps among patients with systemic sclerosis-interstitial lung disease and inform future educational interventions and research.

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Background: Social risk factors are linked to adverse health outcomes, but their total impact on long-term quality of life is obscure. We hypothesized that a higher burden of social risk factors is associated with greater decline in quality of life over 10 years.

Methods: We examined associations between social risk factors count and decline >5 points in (i) physical component summary, and (ii) mental component summary scores from the Short Form-12 among Black and White participants in the Reasons for Geographic and Racial Differences in Stroke study (n = 14 401).

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Article Synopsis
  • The study explores the current practices and attitudes of interstitial lung disease (ILD) clinicians towards improving health-related quality of life (HRQOL) for patients with Hypersensitivity Pneumonitis (HP).
  • Nearly all respondents (100%) believe that interventions to enhance HRQOL are essential, but only 5% currently use validated HRQOL assessment tools.
  • Most clinicians reported limited knowledge of behavioral interventions, such as peer coaching and cognitive behavioral therapy (CBT), yet a significant majority expressed a desire to educate patients about these methods and reinforce them post-treatment.
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Introduction: Medication regimen complexity may be an important risk factor for adverse outcomes in older adults with heart failure. However, increasing complexity is often necessary when prescribing guideline-directed medical therapy at the time of a heart failure hospitalization. We sought to determine whether increased medication regimen complexity following a heart failure hospitalization was associated with worse post-hospitalization outcomes.

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Objectives: Contributors to disparities and worse cervical cancer outcomes include limited education and loss to follow-up after an abnormal Pap smear. Effective interventions are necessary to engage diverse populations. The authors piloted an intervention to assess acceptability, knowledge uptake, and follow-up.

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Background: The Pooled Cohort Equations (PCEs) do not accurately estimate atherosclerotic cardiovascular disease (ASCVD) risk in certain populations. The 2018 AHA/ACC cholesterol guideline identified risk-enhancing factors as a supplement to PCEs-based risk assessment. However, the role of each risk-enhancing factor in ASCVD risk assessment has not been well quantified.

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Article Synopsis
  • The study aimed to address the impact of knowledge gaps on patients' quality of life regarding hypersensitivity pneumonitis (HP) by identifying what information they feel is most lacking.
  • It involved 21 English-speaking patients with HP participating in virtual group sessions to prioritize their information needs.
  • The main knowledge gaps identified were about the disease's natural history, treatment options, epidemiology, coping strategies, symptom management, exposure mitigation, and educational methods for spreading awareness about HP.
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  • The study focuses on improving care transitions for heart failure patients by implementing an intervention called I-TRANSFER-HF, which combines early home health care (HHC) nurse visits with outpatient medical follow-up to reduce hospital readmissions.
  • It employs a Hybrid Type 1, stepped wedge randomized trial design, involving multiple hospital and home health agency (HHA) pairs across the US, to measure the effectiveness of the intervention on readmission rates and patient outcomes.
  • Additionally, the study aims to understand the factors affecting the implementation of I-TRANSFER-HF through qualitative interviews with key stakeholders, using the Consolidated Framework for Implementation Research 2.0 to guide the analysis.
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Background: Fragmentation of care (that is, the use of multiple ambulatory providers without a dominant provider) may increase the risk of gaps in communication among providers. However, it is unclear whether people with fragmented care (as measured in claims) perceive more gaps in communication among their providers. It is also unclear whether people who perceive gaps in communication experience them as clinically significant (that is, whether they experience adverse events that they attribute to poor coordination).

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Objective: The objective of this study is to outline the training of peer coaches in the Moving Well intervention, which was designed to reduce anxiety, depression, and pain catastrophizing in patients before and after total knee replacement (TKR).

Methods: Selected peer coaches had a history of knee osteoarthritis (KOA), a TKR of 12 months or more before training, and were 60 or older. Training was primarily conducted virtually, with a later addition of one in-person session.

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  • This study examines racial differences in comorbidities among individuals with heart failure (HF), specifically focusing on the role of social determinants of health (SDOH) in these disparities.
  • Researchers analyzed data from Black and White participants aged 45 and older who were hospitalized for heart failure between 2003 and 2017 to identify variations in health conditions like diabetes and hypertension.
  • The findings indicate that socioeconomic status partially explains higher rates of diabetes, anemia, and chronic kidney disease in Black adults with preserved ejection fraction (HFpEF), but other SDOH did not significantly account for differences in other health issues.
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  • The study investigates how having multiple medications (polypharmacy) affects the use of guideline-directed medical therapy (GDMT) in patients with heart failure (HF).
  • Researchers analyzed data from 545 hospitalized participants with reduced ejection fraction HF from a specific study covering 2003 to 2017 and looked at their medication counts and GDMT usage.
  • Results showed that a significant portion of patients were not receiving recommended medications, and higher medication counts were linked to lower rates of initiation for these needed therapies.
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  • - Cognitive impairment is prevalent in adults with heart failure (HF) and can lead to worse health outcomes, but the specific pattern of cognitive decline following a first HF hospitalization had not been thoroughly studied.
  • - In a study involving nearly 24,000 participants aged 45 and older, those who experienced HF hospitalization showed a more rapid decline in overall cognitive function (measured by the Six-Item Screener) over five years compared to those without HF hospitalization, even after accounting for other factors.
  • - However, this faster cognitive decline was not observed in specific memory tasks (Word List Learning and Delayed Recall), suggesting that while general cognitive health is affected by HF hospitalization, certain cognitive domains may remain relatively stable.
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Article Synopsis
  • N-of-1 trials provide a personalized way for patients to compare the effectiveness of treatments using their own health data, particularly in the context of managing heart failure with preserved ejection fraction (HFpEF).
  • The study involved qualitative interviews with patients participating in these trials to refine a data visualization tool that helps them understand their treatment results, promoting informed decision-making about their medication.
  • Feedback from participants revealed key preferences for the visualization tool, including clear symptom scores, helpful reference images, and the use of descriptive language to convey changes in health instead of just numerical data.
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  • The study looked at how untreated depression affects people's visits to doctors and specialists.
  • They found that older adults with untreated depression didn't visit specialists as much and were less likely to see a psychiatrist compared to those who were treated.
  • The results show that these patients aren't getting enough help for their depression, and they may not be seeking out more care than needed.
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  • Physicians often struggle with underprescribing and patients not taking medications due to concerns about side effects, but there's little research on how to address these issues.
  • Interviews with doctors revealed that poor communication and conflicting information from families hinder discussions about side effects, while guiding questions and open communication improve the process.
  • The study identified major hurdles in determining the cause of side effects and suggested that improving communication and structured approaches can enhance heart failure medication management.
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Rationale And Objective: Disease-specific health-related quality of life (HRQOL) instruments enable us to capture domains that are most relevant to specific patient populations and are useful when a more individualised approach to patient assessment is desired. In this study, we assessed the validity and reliability of the first instrument specifically developed to measure HRQOL in hypersensitivity pneumonitis (HP).

Methods: A 39-item HP-HRQOL instrument and several anchors were collected from a cohort of patients with HP.

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