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Dive into the research topics where Barbara DiCicco-Bloom is active.

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Featured researches published by Barbara DiCicco-Bloom.


Medical Education | 2006

The qualitative research interview

Barbara DiCicco-Bloom; Benjamin F. Crabtree

Background  Interviews are among the most familiar strategies for collecting qualitative data. The different qualitative interviewing strategies in common use emerged from diverse disciplinary perspectives resulting in a wide variation among interviewing approaches. Unlike the highly structured survey interviews and questionnaires used in epidemiology and most health services research, we examine less structured interview strategies in which the person interviewed is more a participant in meaning making than a conduit from which information is retrieved.


Annals of Family Medicine | 2005

Social Network Analysis as an Analytic Tool for Interaction Patterns in Primary Care Practices

John G. Scott; Alfred F. Tallia; Jesse C. Crosson; A. John Orzano; Christine Stroebel; Barbara DiCicco-Bloom; Dena O’Malley; Eric K. Shaw; Benjamin F. Crabtree

PURPOSE Social network analysis (SNA) provides a way of quantitatively analyzing relationships among people or other information-processing agents. Using 2 practices as illustrations, we describe how SNA can be used to characterize and compare communication patterns in primary care practices. METHODS Based on data from ethnographic field notes, we constructed matrices identifying how practice members interact when practice-level decisions are made. SNA software (UCINet and KrackPlot) calculates quantitative measures of network structure including density, centralization, hierarchy and clustering coefficient. The software also generates a visual representation of networks through network diagrams. RESULTS The 2 examples show clear distinctions between practices for all the SNA measures. Potential uses of these measures for analysis of primary care practices are described. CONCLUSIONS SNA can be useful for quantitative analysis of interaction patterns that can distinguish differences among primary care practices.


Annals of Family Medicine | 2008

Understanding Healing Relationships in Primary Care

John G. Scott; Deborah J. Cohen; Barbara DiCicco-Bloom; William L. Miller; Kurt C. Stange; Benjamin F. Crabtree

PURPOSE Clinicians often have an intuitive understanding of how their relationships with patients foster healing. Yet we know little empirically about the experience of healing and how it occurs between clinicians and patients. Our purpose was to create a model that identifies how healing relationships are developed and maintained. METHODS Primary care clinicians were purposefully selected as exemplar healers. Patients were selected by these clinicians as having experienced healing relationships. In-depth interviews, designed to elicit stories of healing relationships, were conducted with patients and clinicians separately. A multidisciplinary team analyzed the interviews using an iterative process, leading to the development of case studies for each clinician-patient dyad. A comparative analysis across dyads was conducted to identify common components of healing relationships RESULTS Three key processes emerged as fostering healing relationships: (1) valuing/creating a nonjudgmental emotional bond; (2) appreciating power/consciously managing clinician power in ways that would most benefit the patient; and (3) abiding/displaying a commitment to caring for patients over time. Three relational outcomes result from these processes: trust, hope, and a sense of being known. Clinician competencies that facilitate these processes are self-confidence, emotional self-management, mindfulness, and knowledge. CONCLUSIONS Healing relationships have an underlying structure and lead to important patient-centered outcomes. This conceptual model of clinician-patient healing relationships may be generalizable to other kinds of healing relationships.


Annals of Family Medicine | 2007

Electronic Medical Records and Diabetes Quality of Care: Results From a Sample of Family Medicine Practices

Jesse C. Crosson; Pamela Ohman-Strickland; Karissa A. Hahn; Barbara DiCicco-Bloom; Eric K. Shaw; A. John Orzano; Benjamin F. Crabtree

PURPOSE Care of patients with diabetes requires management of complex clinical information, which may be improved by the use of an electronic medical record (EMR); however, the actual relationship between EMR usage and diabetes care quality in primary care settings is not well understood. We assessed the relationship between EMR usage and diabetes care quality in a sample of family medicine practices. METHODS We conducted cross-sectional analyses of baseline data from 50 practices participating in a practice improvement study. Between April 2003 and December 2004 chart auditors reviewed a random sample of medical records from patients with diabetes in each practice for adherence to guidelines for diabetes processes of care, treatment, and achievement of intermediate outcomes. Practice leaders provided medical record system information. We conducted multivariate analyses of the relationship between EMR usage and diabetes care adjusting for potential practice- and patient-level confounders and practice-level clustering. RESULTS Diabetes care quality in all practices showed room for improvement; however, after adjustment, patient care in the 37 practices not using an EMR was more likely to meet guidelines for process (odds ratio [OR], 2.25; 95% confidence interval [CI], 1.42–3.57) treatment (OR, 1.67; 95% CI, 1.07–2.60), and intermediate outcomes (OR, 2.68; 95% CI, 1.49–4.82) than in the 13 practices using an EMR. CONCLUSIONS The use of an EMR in primary care practices is insufficient for insuring high-quality diabetes care. Efforts to expand EMR use should focus not only on improving technology but also on developing methods for implementing and integrating this technology into practice reality.


Annals of Family Medicine | 2005

Delivery of Clinical Preventive Services in Family Medicine Offices

Benjamin F. Crabtree; William L. Miller; Alfred F. Tallia; Deborah J. Cohen; Barbara DiCicco-Bloom; Helen E. McIlvain; Virginia A. Aita; John G. Scott; Patrice Gregory; Kurt C. Stange; Reuben R. McDaniel

BACKGROUND This study aimed to elucidate how clinical preventive services are delivered in family practices and how this information might inform improvement efforts. METHODS We used a comparative case study design to observe clinical preventive service delivery in 18 purposefully selected Midwestern family medicine offices from 1997 to 1999. Medical records, observation of outpatient encounters, and patient exit cards were used to calculate practice-level rates of delivery of clinical preventive services. Field notes from direct observation of clinical encounters and prolonged observation of the practice and transcripts from in-depth interviews of practice staff and physicians were systematically examined to identify approaches to delivering clinical preventive services recommended by the US Preventive Services Task Force. RESULTS Practices developed individualized approaches for delivering clinical preventive services, with no one approach being successful across practices. Clinicians acknowledged a 3-fold mission of providing acute care, managing chronic problems, and prevention, but only some made prevention a priority. The clinical encounter was a central focus for preventive service delivery in all practices. Preventive services delivery rates often appeared to be influenced by competing demands within the clinical encounter (including between different preventive services), having a physician champion who prioritized prevention, and economic concerns. CONCLUSIONS Practice quality improvement efforts that assume there is an optimal approach for delivering clinical preventive services fail to account for practices’ propensity to optimize care processes to meet local contexts. Interventions to enhance clinical preventive service delivery should be tailored to meet the local needs of practices and their patient populations.


Journal of Transcultural Nursing | 2004

The racial and gendered experiences of immigrant nurses from Kerala, India.

Barbara DiCicco-Bloom

The purpose of this article is to describe the experiences of a group of immigrant women nurses regarding their life and work in a culture other than their own. Semistructured, in-depth interviews were conducted with nurses who were born in Kerala, India, educated in India, and are actively employed as nurses in the United States. The participants told stories that were about (a) the challenges of living between two cultures and countries, (b) the racism they experience, and (c) their marginalization as female nurses of color. This study underscores the continuing inequities of our health care system. Our challenge is to establish a more just and effective environment for those who provide care as well as those who receive it.


Journal of General Internal Medicine | 2008

Variation in Electronic Prescribing Implementation Among Twelve Ambulatory Practices

Jesse C. Crosson; Nicole Isaacson; Debra Lancaster; Emily A. McDonald; Anthony J. Schueth; Barbara DiCicco-Bloom; Joshua L. Newman; C. Jason Wang; Douglas S. Bell

BackgroundElectronic prescribing has been advocated as an important tool for improving the safety and quality of medication use in ambulatory settings. However, widespread adoption of e-prescribing in ambulatory settings has yet to be realized. The determinants of successful implementation and use in these settings are not well understood.ObjectiveTo describe the practice characteristics associated with implementation and use of e-prescribing in ambulatory settings.DesignMulti-method qualitative case study of ambulatory practices before and after e-prescribing implementation.ParticipantsSixteen physicians and 31 staff members working in 12 practices scheduled for implementation of an e-prescribing program and purposively sampled to ensure a mix of practice size and physician specialty.MeasurementsField researchers used observational and interview techniques to collect data on prescription-related clinical workflow, information technology experience, and expectations.ResultsFive practices fully implemented e-prescribing, 3 installed but with only some prescribers or staff members using the program, 2 installed and then discontinued use, 2 failed to install. Compared to practice members in other groups, members of successful practices exhibited greater familiarity with the capabilities of health information technologies and had more modest expectations about the benefits likely to accrue from e-prescribing. Members of unsuccessful practices reported limited understanding of e-prescribing capabilities, expected that the program would increase the speed of clinical care and reported difficulties with technical aspects of the implementation and insufficient technical support.ConclusionsPractice leaders should plan implementation carefully, ensuring that practice members prepare for the effective integration of this technology into clinical workflow.


Quality management in health care | 2002

Assessing diversity and quality in primary care through the multimethod assessment process (MAP).

Jo Ann Kairys; John Orzano; Patrice Gregory; Christine Stroebel; Barbara DiCicco-Bloom; Beatrix Roemheld-Hamm; Fred A. Kobylarz; John G. Scott; Lisa Coppola; Benjamin F. Crabtree

The U.S. health care system serves a diverse population, often resulting in significant disparities in delivery and quality of care. Nevertheless, most quality improvement efforts fail to systematically assess diversity and associated disparities. This article describes application of the multimethod assessment process (MAP) for understanding disparities in relation to diversity, cultural competence, and quality improvement in clinical practice. MAP is an innovative quality improvement methodology that integrates quantitative and qualitative techniques and produces a system level understanding of organizations to guide quality improvement interventions. A demonstration project in a primary care practice illustrates the utility of MAP for assessing diversity.


Journal of Cancer Survivorship | 2013

The experience of information sharing among primary care clinicians with cancer survivors and their oncologists.

Barbara DiCicco-Bloom; Regina S. Cunningham

Purpose of studyKnowledge about information sharing among primary care clinicians, oncologists, and their cancer patients is critical given its importance in facilitating the delivery of quality care to the increasing number of cancer survivors. The purpose of our study was to provide a better understanding of the nature of interactions among primary care clinicians, patients, and oncologists throughout the cancer care continuum to better understand the transition to survivorship.MethodTwenty-one qualitative in-depth interviews were conducted with 11 primary care physicians and 10 nurse practitioners. Themes were identified using content analysis.ResultsThe following themes emerged from the data including: (1) a visit is worth a thousand written reports—primary care clinicians described the importance of patient visits during cancer treatment; (2) community vs. cancer center oncologists—primary care clinicians described differences in information sharing with community oncologists as compared with those in academic centers; (3) correcting for information deficits—primary care clinicians, unable to obtain regular progress reports directly from oncologists, developed indirect strategies to obtain information; (4) the deficiencies in post-treatment follow-up care plans; and (5) the panacea of electronic medical records and survivor care plans.ConclusionsThe themes that emerged from this work describe in detail the absence of systematic information sharing among primary care clinicians, patients, and oncologists that is needed to support quality survivorship care in the primary care setting. The descriptions by primary care clinicians contribute to a deeper understanding of the daily challenges that both interfere and/or support primary care clinicians in their care of survivors of cancer.Implications for cancer survivorsManaging the complex care of cancer survivors often requires the expertise of a number of skilled providers. Information sharing among these individuals is one of the most fundamental aspects of ensuring effective transitions in care. Our results indicate that systematic information sharing among providers caring for cancer survivors is lacking. Identifying strategies to enhance information sharing among and between providers is essential to facilitating the delivery of high-quality survivor care.


Home Health Care Management & Practice | 2000

Practical Approaches to Developing Cultural Competency

Barbara DiCicco-Bloom

The same demographic trends and cultural changes that have caused government agencies and private sector businesses to train their associates to be culturally competent are affecting the nursing profession. The patient-centered orientation of nurses makes it essential that they also be culturally competent by accessing cultural knowledge and developing cultural skills. What follows are vignettes and personal experiences based on a study by the author in which nurses were observed providing home care to newly admitted, culturally diverse patients. Tools for cultural assessment are described and included, along with recommendations to enhance the cultural competence of home care nurses and home care agencies.

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John G. Scott

University of Medicine and Dentistry of New Jersey

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A. John Orzano

University of Medicine and Dentistry of New Jersey

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