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<title>Graduate School of Nursing Dissertations</title>
<copyright>Copyright (c) 2013 University of Massachusetts Medical School All rights reserved.</copyright>
<link>http://escholarship.umassmed.edu/gsn_diss</link>
<description>Recent documents in Graduate School of Nursing Dissertations</description>
<language>en-us</language>
<lastBuildDate>Sun, 21 Apr 2013 01:34:49 PDT</lastBuildDate>
<ttl>3600</ttl>


	
		
	







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<title>Transitioning Through Middle Age with an Incomplete Spinal Cord Injury: A Qualitative Description of Changes in Physical Function: A Dissertation</title>
<link>http://escholarship.umassmed.edu/gsn_diss/28</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/gsn_diss/28</guid>
<pubDate>Fri, 19 Apr 2013 13:29:02 PDT</pubDate>
<description>
	<![CDATA[
	<p>Over 260,000 Americans are living with a traumatic spinal cord injury (SCI). Medical advances have increased the longevity of individuals living with SCI into middle age and beyond. The majority of these individuals are living with an incomplete SCI (NSCISC, 2012), and the proportion of incomplete injuries is rising (DeVivo, 2012). There is little research that specifically examines the changes in physical function experienced by individuals aging with a traumatic incomplete SCI. The purpose of this qualitative descriptive study was to describe the changes in physical function experienced by participants with a traumatic incomplete SCI aging through middle age. Data were collected through moderately structured individual interviews (N=17), in either a face-to-face (n=6) or an email (n=11) format. The seventeen participants ranged in age from 35 to 65 years, with a 16 to 36 year duration of injury. Participants described changes in various body systems and recalled the timing of those changes as they transitioned through their middle years. Qualitative content analysis revealed that participants described primarily gradual changes including decreased muscle strength, decreased endurance, weight gain, and wear and tear changes. When asked to identify sources of information about physical changes, participants predominantly emphasized their lack of knowledge about anticipated changes. Further content analysis revealed three themes related to this transition. Participants likened their experience to <em>travelling through uncharted territory.</em> They described <em>strategies for living in uncharted territory</em> that help them to prevent or manage changes in physical function, with sub-themes of <em>being vigilant</em> in their self-assessment and self-management practices, investing time in <em>figuring out</em> what changes they experienced and why those changes happened, and <em>staying positive.</em> They also described the importance of <em>recognizing the impact of changes.</em> These findings provide a foundation for understanding this age-related transition, and identify the need for further research to support effective self-management strategies and efficient mechanisms for disseminating this knowledge to people with SCI, their caregivers and families. In acute and chronic patient care settings, nurses are well-positioned to be a valuable support and information source for individuals living with an incomplete SCI.</p>

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</description>

<author>Deborah K. Armstrong</author>


<category>Dissertations, UMMS</category>

<category>Spinal Cord Injuries</category>

<category>Aging</category>

<category>Middle Aged</category>

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<title>The Experience of the Health Care Team Members Involved in Facial Transplant Surgery and Patient Care: A Dissertation</title>
<link>http://escholarship.umassmed.edu/gsn_diss/27</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/gsn_diss/27</guid>
<pubDate>Mon, 01 Oct 2012 07:15:23 PDT</pubDate>
<description>
	<![CDATA[
	<p>The attitudes and experiences of the health care team members involved in facial transplant surgery and patient care were explored in this study, which utilized a qualitative descriptive method. The Specific Aims of the study and the interview questions were guided by “Moore’s Ethical Criteria for Surgical Innovation.” Overall, the participants believed that the risk-benefit ratio of facial transplantation favored proceeding with the procedure in the clinical scenarios with which they had been exposed. The participant’s experience was challenging and rewarding, and they expressed personal fulfillment from the opportunity to be involved in the transformation of another human being’s life. Moreover, the entire effort exhibited highly effective team work which displayed <em>esprit de corps</em>, was guided by superior leadership, and illuminated the importance of the clinical, intellectual, and historical environment of the institution where the procedures took place. These components represent a “surgical innovation cluster,” a proposed framework for guiding surgical innovative efforts which represent major paradigmatic shifts in both scientific effort and social philosophy.</p>

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</description>

<author>Linda A. Evans</author>


<category>Dissertations, UMMS</category>

<category>Facial Transplantation</category>

<category>Patient Care Team</category>

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<item>
<title>Cardiovascular Risk Factor Knowledge, Risk Perception, and Actual Risk in HIV-Infected Patients: A Dissertation</title>
<link>http://escholarship.umassmed.edu/gsn_diss/26</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/gsn_diss/26</guid>
<pubDate>Mon, 01 Oct 2012 07:15:22 PDT</pubDate>
<description>
	<![CDATA[
	<p>Background: Cardiovascular disease (CVD) has emerged as a major cause of morbidity and mortality in HIV-infected adults. Research in noninfected populations suggests that knowledge of CVD risk factors significantly influences perception of risk. Understanding the level of risk factor knowledge and risk perception can inform the development of innovative interventions to reduce risk. The purpose of this study was to describe cardiovascular risk factor knowledge and risk perception in a cohort of HIV-infected adults.</p>
<p>Specific aims included (a) describing the estimated risk of CVD, the perceived risk of CVD, and the level of CVD risk factor knowledge; (b) describing the relationship between estimated and perceived risk, and (c) examining the influence of risk factor knowledge on perceived risk of CVD. The Health Belief Model was the theoretical framework that guided the study.</p>
<p>Methods: A prospective observational cohort; cross-sectional design. A convenience sample of 130 HIV-infected adults was recruited from two hospital-based HIV clinics. Each participant had one study visit in which all data were collected by direct interview.</p>
<p>Results: Results: Mean age of enrollees was 48 years (SD 8.4); 62% were male; 41.5% White, 32% Black, 23% Hispanic; 56% current smokers; mean years since HIV diagnosis were 14.7; mean BMI 27 (SD 5.5); 48.5% had prehypertension. Higher scores on the Heart Disease Fact Questionnaire indicate a higher degree of knowledge. In this sample, the Mean was 19, (S.D. 3.5; range 6–25), indicating a fair degree of knowledge. Estimated and perceived risk were significantly, though weakly, correlated <em>r</em> (126) = .24, <em>p</em> = .01. Controlling for age, risk factor knowledge was not predictive of perceived risk (F[1,117] = 0.13, p > .05).</p>
<p>Conclusions: HIV-infected adults are at increased risk for cardiovascular disease. Traditional CVD risk factors such as smoking, prehypertension, and being overweight are highly prevalent. Despite having a fair level of risk factor knowledge, knowledge did not influence perception of risk for CVD. Research to improve risk perception and to develop innovative interventions that reduce CVD risk is needed for this population.</p>

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</description>

<author>Patricia A. Cioe</author>


<category>Dissertations, UMMS</category>

<category>Cardiovascular Diseases</category>

<category>HIV Infections</category>

<category>Risk Factors</category>

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<title>The Role of School Nurses in the Early Identification, Referral and Provision of Services for Students with Early Signs of Mental, Emotional or Behavioral Disorders: A Dissertation</title>
<link>http://escholarship.umassmed.edu/gsn_diss/25</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/gsn_diss/25</guid>
<pubDate>Fri, 28 Sep 2012 11:35:24 PDT</pubDate>
<description>
	<![CDATA[
	<p>The purpose of this qualitative study was to explore school nurses’ (SN) perceptions of factors influencing their ability to identify, refer, and provide mental health services to students with <em>early</em> signs of mental, emotional, and behavioral (MEB) needs. The National Research Council and Institute of Medicine have urged a <em>preventive</em> public health approach to decrease adverse outcomes of unidentified and untreated MEB needs among children (O’Connell, 2009). Historically and theoretically based in public health, SN have daily contact with students and are in an optimal location for early identification, referral and provision of services, yet little empirical research describing their role is available.</p>
<p>Five focus groups with 29 SN were conducted and four themes emerged through analysis of data: <em>Frequent flyers</em> : student visits to SN offices, the observations that alert SN to potential MEB needs; <em>Digging to get the whole picture</em> : the process SN frequently used to collect information necessary to confirm MEB needs; <em>Road to referral</em> : the resources used and barriers encountered within the referral process; and, <em>Safety zone</em> : the important role SN play in the provision of services to students with early signs of MEB needs. Within the provision of services was a collective subtheme across all five focus groups: <em>What we need to better help our kids.</em> In this category SN identified their educational limitations and learning needs, as well as potential strategies to improve provision of services for students with MEB needs.</p>
<p>The findings of this study provide a lens into the complex and little explored are of early identification, referral and intervention processes used by SN to care for students with MEB needs. Understanding the role of the SN is a critical first step towards improving outcomes.</p>

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</description>

<author>Susan Boland-Shepherd</author>


<category>Dissertations, UMMS</category>

<category>School Nursing</category>

<category>Students</category>

<category>Mental Health Services</category>

<category>Early Medical Intervention</category>

<category>Mental Disorders</category>

<category>Children</category>

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<title>Factors Influencing Long-Term Health-Related Quality of Life Among Patients After Aneurysmal and Nonaneurysmal Subarachnoid Hemorrhage: A Dissertation</title>
<link>http://escholarship.umassmed.edu/gsn_diss/24</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/gsn_diss/24</guid>
<pubDate>Mon, 12 Mar 2012 12:53:00 PDT</pubDate>
<description>
	<![CDATA[
	<p>Subarachnoid hemorrhage (SAH) causes 5% of all strokes and is responsible for about 18,000 deaths per year in the United States (Aneurysmal Subarachnoid Hemorrhage, 2008). The incidence of SAH has been estimated at 6 to 8 per 100,000 persons per year (Linn, Rinkel, Algra, & van Gijn, 1996). In nearly 15% (range 5–34%) of patients with SAH, no source of hemorrhage can be identified via four-vessel cerebral angiography (Alen et al., 2003; Gupta et al., 2009), resulting in two major types of SAH: aneurysmal (ASAH) and nonaneurysmal (NASAH). Anecdotal evidence and contradictory research suggest that patients with NASAH experience some of the same health-related quality of life (HRQOL) issues as patients with ASAH. The purpose of this quantitative survey design study was to compare health-related quality of life (HRQOL) 1 to 3 years post-hemorrhage in patients who have experienced a NASAH to those who have experienced an ASAH. This is the first US study to specifically investigate HRQOL in NASAH and the second study comparing HRQOL outcomes between aneurysmal and nonaneurysmal subarachnoid hemorrhage patients. Our results are comparable to the first study by Hutter and Gilsbach, (1995), which also found that the two groups are much more similar than different. There were no significant differences between 28 of the 36 demographic and clinical characteristics examined in this study. Our study confirms previous findings that there is a significant impact on employment for both hemorrhage groups and an even greater inability to return to work for the NASAH patients. The nonaneurysmal group had more physical symptom complaints while the aneurysmal group had more emotional symptoms. Lastly, both groups had low levels of PTSD, and these levels did not differ significantly between groups. However, PTSD and social support were shown by regression analysis to impact HRQOL for both groups. We recommend that clinicians assess for PTSD in all subarachnoid hemorrhage patients and institute treatment early, which will decrease the negative effects on HRQOL. This may include offering psychological services or social work early in the hospital course to all SAH patients. Further research and policy changes are needed to assist in interventions that improve vocational reintegration after SAH. NASAH patients should no longer be referred to as having suffered a “benign hemorrhage.” They have had a life changing hemorrhage that may forever change their lives and impact their HRQOL.</p>

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</description>

<author>Arthur P. McIntosh</author>


<category>Dissertations, UMMS</category>

<category>Subarachnoid Hemorrhage</category>

<category>Health Status</category>

<category>Health Status Indicators</category>

<category>Quality of Life</category>

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<title>Women’s Experiences of Discontinuing Hormone Therapy: A Dissertation</title>
<link>http://escholarship.umassmed.edu/gsn_diss/23</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/gsn_diss/23</guid>
<pubDate>Thu, 15 Dec 2011 06:38:06 PST</pubDate>
<description>
	<![CDATA[
	<p>Although many women find relief from menopause through hormone therapy (HT), current guidelines recommend that HT be used only for short-term relief of symptoms. Women who attempt to stop HT often encounter troublesome recurrent symptoms leading to a diminished quality of life (QoL); 25% of women who discontinue eventually resume HT. Unfortunately, there is little information for women and their health care providers as to the best way to discontinue HT or how to prepare and guide women through this process. An in-depth description of women‘s experiences during HT discontinuation and the factors influencing recurrent symptoms, QoL and discontinuation outcome would provide knowledge to develop much needed counseling and support interventions. The purpose of this study was to explore women‘s experiences discontinuing hormone therapy for menopause.</p>
<p>This Internet-based mixed-methods study used a dominant Qualitative Descriptive design with embedded quantitative QoL measurements. Participants completed the quantitative questionnaires online while open-ended questions were completed either online or by telephone. Interview data were analyzed through Qualitative Content Analysis; descriptive statistics were used to explore the quantitative measures. Participants were stratified by discontinuation status for comparison of variations in discontinuation experiences, QoL and influencing factors.</p>
<p>Thirty-four women (20 stopped, 9 resumed, 4 tapering) were enrolled. One overarching theme--'a solitary journey'--emerged: although all women embarked on this journey, each woman traveled her own path. Two subthemes--'burden and interference' and 'appraising risk'--encompassed the symptom factors (severity, interference and sensitivity) that influenced women's experiences and the manner in which women evaluated their options. Other influencing factors included: readiness viii and reasons for stopping HT, beliefs about menopause and roles. QoL was strongly connected to symptoms for many but not all women. Information from health care providers was inconsistent; women desired more support from providers and other women.</p>
<p>The rich description of women's experiences stopping HT highlights the need for providers to assess women's sensitivity to symptoms and readiness to discontinue to determine which women might benefit from more support. Greater health literacy would enhance women's understanding of HT risks. More research is needed on symptom clusters and interference and strategies for minimizing their impact.</p>

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</description>

<author>Mary A. Fischer</author>


<category>Dissertations, UMMS</category>

<category>Menopause</category>

<category>Postmenopause</category>

<category>Estrogen Replacement Therapy</category>

<category>Quality of Life</category>

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<title>The Role of the Mass Media in Women’s Infant Feeding Decisions: A Dissertation</title>
<link>http://escholarship.umassmed.edu/gsn_diss/22</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/gsn_diss/22</guid>
<pubDate>Mon, 19 Sep 2011 06:03:24 PDT</pubDate>
<description>
	<![CDATA[
	<p>Breastfeeding has been established as providing the best and most complete nutrition for newborns, as this method promotes the infant’s health and supports infant growth (American Academy of Pediatrics [AAP], 2005). Mass media have been suggested as powerful and universal means of communication with the potential to impact social norms. Thus, this qualitative descriptive study explored, within the context of the Socioecological Framework, women’s decision making on whether to breastfeed or bottle-feed their infants and the effect of mass media on their decision.</p>
<p>Data were collected in individual audiotaped interviews with participants recruited from the Massachusetts Breastfeeding Coalition and UMass Memorial Medical Center. Interview data were compared to text and visual representation from 12 Internet sites on parenting and infant feeding. Data analysis was conducted simultaneously with data collection and was continued until saturation was achieved. The comparison findings demonstrated that the emerging themes from the participant interviews reflected the information represented on the Internet sites.</p>
<p>The main theme <em>Media Matters Not </em>suggested that mass media did not influence infant feeding decisions for this group of mothers. What did have an important impact on infant feeding decisions was the information and emotional support provided by partners, family, and HCPs (subtheme of <em>Influences on Decisions</em>). The participants offered suggestions of media messages they would like see in the future such as public service announcements of women breastfeeding their infants. In addition, the participants discussed media issues that had potential for influencing infant feeding decisions (<em>Media Messages—Good and Bad</em>), emphasized the need for public opinion to be altered so that breastfeeding in public would be viewed as more acceptable (<em>Community/Public Opinions</em>), and described suggestions for enhancing media messages about breastfeeding (<em>Recommendations for Future Media Messages</em>). The implications for nursing practice, public policy, and future research related to the topic were discussed.</p>

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</description>

<author>Paula Bylaska-Davies</author>


<category>Breast Feeding</category>

<category>Bottle Feeding</category>

<category>Infant</category>

<category>Mothers</category>

<category>Infant Care</category>

<category>Maternal Behavior</category>

<category>Decision Making</category>

<category>Mass Media</category>

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<title>Exploring Healthcare Experiences of Lesbian, Gay, and Bisexual College Students Using Community-Based Participatory Research: A Dissertation</title>
<link>http://escholarship.umassmed.edu/gsn_diss/21</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/gsn_diss/21</guid>
<pubDate>Thu, 15 Sep 2011 08:53:21 PDT</pubDate>
<description>
	<![CDATA[
	<p>Little is known about the healthcare experiences of lesbian, gay, and bisexual (LGB) young adults (ages 18-24) and even less is known about LGB college students (ages 18-24). Helping LGB college students effectively access appropriate, sensitive healthcare has the potential to reduce negative long-term health consequences. Therefore, the purpose of this study was to describe the healthcare experiences of LGB college students (ages 18-24) in the local college community using community-based participatory research (CBPR). Three online synchronous focus groups and one online individual interview were conducted with 19 LGB college students between January and February 2011. The focus groups were segmented into lesbian (<em>n</em>= 7), gay (<em>n</em>= 7), and female bisexual (<em>n</em> = 4) groups. One male bisexual was interviewed individually. The mean age of the sample was 20.7 years (SD = 1.2, range = 19-24). The sample was predominately White non-Hispanic (85%).</p>
<p>Qualitative content analysis was used to describe the healthcare experiences of lesbian, gay, and bisexual college students in the local community. One overarching theme (not all the same), one main theme (comfort during the clinical encounter), three sub themes (personalizing the clinical encounter, deciding to disclose and social stigma, and seeking support of self-identified sexual orientation) and one preliminary sub theme (perceived confidentiality) emerged from the analysis. One major action emerged from the analysis and supported the development of the social network site (on Facebook) entitled: College Alliance Towards Community Health (CATCH). The mission of CATCH is to provide LGB college students in the local community with a comfortable forum to learn about various healthcare concerns of lesbian, gay, and bisexual college students. Additional implications for nursing practice and implications for further research in the LGB college community are addressed.</p>

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</description>

<author>Caitlin M. Stover</author>


<category>Dissertations, UMMS</category>

<category>Homosexuality, Female</category>

<category>Homosexuality, Male</category>

<category>Bisexuality</category>

<category>Students</category>

<category>Health Services Needs and Demand</category>

<category>Health Status Indicators</category>

<category>Community-Based Participatory Research</category>

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<title>Patient Safety: A Multi-Climate Approach to the Nursing Work Environment: A Dissertation</title>
<link>http://escholarship.umassmed.edu/gsn_diss/20</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/gsn_diss/20</guid>
<pubDate>Tue, 07 Jun 2011 08:00:46 PDT</pubDate>
<description>
	<![CDATA[
	<p>The purpose of this study was to explore Zohar’s Multi-Climate Framework for Occupational Safety to determine the effects of staff nurse perceptions of safety priorities in their organization (safety climate) and their work ownership climate (Magnet Hospital designation) on safety citizenship behaviors viewed as in role or extra role. Safety citizenship behaviors are described as behaviors that go beyond the job description to ensure safety. Participants from a convenience sample of three Magnet designated community hospitals in New England completed three scales (Zohar’s Safety Climate Questionnaire, Essentials of Magnetism II and the Safety Citizenship Role Definitions Scale) representing the study variables via an online survey platform. Multivariate analysis of covariance informed the results. Findings include a positive unadjusted relationship between safety climate and work ownership climate (<em>r<sub>s</sub></em>=.492, <em>p</em><.001, N=92). Zohar’s model was not supported in this study as the interaction of safety climate and work ownership climate on nurse’s views about safety behaviors as in role versus extra role was not statistically significant (p=0.143). However, results did indicate that work environment alone exerted a small (effect size = .09) but significant role in predicting whether nurses viewed safety behaviors as in role versus extra role (<em>F</em> (1, 86) = 8.4, <em>p</em>=.005, N=92), controlling for work ownership climate and hospital. Implications include support for a continued focus on better understanding the importance of a positive nursing work environment, a characteristic shared by Magnet designated hospitals, on the presence of safety citizenship behaviors in the acute care environment. A professional work environment should be considered as an important factor in reducing errors in the acute care setting.</p>

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</description>

<author>Barbara H. Weatherford</author>


<category>Occupational Health</category>

<category>Safety</category>

<category>Safety Management</category>

<category>Nursing Staff</category>

<category>Nurses</category>

<category>Workplace</category>

<category>Dissertations, UMMS</category>

</item>






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<title>Parents of Children Newly Diagnosed with T1DM:
Experiences with Social Support and Family Management: A Dissertation</title>
<link>http://escholarship.umassmed.edu/gsn_diss/19</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/gsn_diss/19</guid>
<pubDate>Fri, 18 Feb 2011 13:55:15 PST</pubDate>
<description>
	<![CDATA[
	<p>The purpose of this mixed-methods descriptive study with parents of children newly diagnosed with Type 1 diabetes was to explore their experiences with peer social support following the Social Support to Empower Parents (STEP) intervention and to examine the usefulness of the Family Management Measure (FaMM) in this population. The specific aims were to describe parents' experiences with the STEP social support intervention, describe parents' day-to-day diabetes management as measured by the FaMM, describe the relationship between parental management scores in the six FaMM dimensions and the social support intervention dose used, and explore FaMM scores in relationship to parent satisfaction with the STEP social support intervention. Identified themes of availability, practical tips, and common ground resonated throughout the interviews with parents and reflected Ireys' emotional, informational, and affirmational social support framework. Regardless of the intervention dose, number of parent mentor contacts, or scores on the FaMM scales, all parents interviewed when questioned, gave a 5/5 for satisfaction with the STEP RCT, qualitatively underscoring the positive effect of the intervention.</p>

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</description>

<author>Ellen M. Rearick</author>


<category>Diabetes Mellitus, Type 1</category>

<category>Child</category>

<category>Parents</category>

<category>Family Health</category>

<category>Social Support</category>

<category>Dissertations, UMMS</category>

</item>






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<title>Nursing Unit Staffing: An Innovative Model Incorporating Patient Acuity and Patient Turnover</title>
<link>http://escholarship.umassmed.edu/gsn_diss/18</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/gsn_diss/18</guid>
<pubDate>Thu, 09 Sep 2010 06:34:37 PDT</pubDate>
<description>
	<![CDATA[
	<p>Changes in reimbursement make it imperative for nurse managers to develop tools and methods to assist them to stay within budget. Disparity between planned staffing and required staffing often requires supplemental staffing and overtime. In addition, many states are now mandating staffing committees to demonstrate effective staff planning. This retrospective quantitative study developed an empirical method for building nursing unit staffing plans through the incorporation of patient acuity and patient turnover as adjustments towards planning nursing workload. The theoretical framework used to guide this study was structural contingency theory (SCT).</p>
<p>Patient turnover was measured by Unit Activity Index (UAI). Patient acuity was measured using case mix index (CMI). Nursing workload was measured as hours per patient day (HPPD). The adjustment to HPPD was made through the derivation of a weight factor based on UAI and CMI. The study consisted of fourteen medical, surgical, and mixed medical-surgical units within a large academic healthcare center. Data from 3 fiscal years were used.</p>
<p>This study found that there were significant, but generally weak correlations between UAI and CMI and HPPD. The method of deriving a weight factor for adjusting HPPD was not as important as the decision-making relative to when to adjust planned HPPD. In addition, the measure of unit activity index was simplified which will assist researchers to more easily calculate patient turnover. As a result of this study, nurse managers and will be better able to adjust and predict HPPD in cases where benchmarking has been problematic. Data-driven adjustments to HPPD based on UAI and CMI will assist the nurse manager to plan and budget resources more effectively.</p>

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</description>

<author>Shirley J. Tierney</author>


<category>Nursing Staff, Hospital</category>

<category>Personnel Staffing and Scheduling</category>

<category>Nursing Administration Research</category>

<category>Workload</category>

<category>Dissertations, UMMS</category>

</item>






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<title>Self-Management of Type 1 Diabetes Across Adolescence: A Dissertation</title>
<link>http://escholarship.umassmed.edu/gsn_diss/17</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/gsn_diss/17</guid>
<pubDate>Thu, 25 Feb 2010 06:59:00 PST</pubDate>
<description>
	<![CDATA[
	<p>Little is known about what variables affect self-management practices of adolescents with T1D. Few studies have examined differences in self-management behaviors by stage of adolescence. Similarly, no studies have examined all of the attributes of self-management, including Collaboration with Parents and Goals. In order to fill the gaps in the literature, a secondary data analysis with a descriptive correlation design was conducted to describe T1D self-management behaviors (Collaboration with Parents, Diabetes Care Activities, Diabetes Problem Solving, Diabetes Communication and Goals) during early, middle and late stages of adolescence. This study also examined whether the roles of covariates (regimen, duration of illness (DOI), gender) in self-management behaviors vary by stage of adolescence. Data from 504 subjects aged 13 – 21 years were analyzed and the age variable was transformed into three adolescent stages early (13-14) (<em>n</em>=163), middle (15-16) (<em>n</em>=159) and late (17-21) (<em>n</em>=182).</p>
<p>The findings revealed significant differences between adolescent stages on Collaboration with Parents and the Diabetes Problem Solving subscale. The covariate analysis showed no significant effect modification for the covariates and stage on any of the subscales so the results did not differ from the ANOVA model. Covariate analysis showed significant associations between regimen and Collaboration with Parents, Diabetes Care Activities and Diabetes Problem Solving. DOI showed significant associations only with Diabetes Problem solving and gender had significant associations with Diabetes Care Activities and Diabetes Communication.</p>
<p>The mean scores on Collaboration with Parents show an incremental decline in collaboration with parents as adolescents move through stages. The higher mean Diabetes Problem Solving scores found in the late adolescent group compared correlated with a higher degree of problem solving in this group when compared to those in the early or middle adolescent stage group. Regimen had significant associations with three of the five subscales suggesting this is an important variable for future study. DOI did not have a significant impact on self-management whereas gender related differences in the areas of Diabetes Activities and Diabetes communication warrant further investigation.</p>

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</description>

<author>Lori A. Keough</author>


<category>Diabetes Mellitus, Type 1</category>

<category>Self Care</category>

<category>Patient Compliance</category>

<category>Adolescent</category>

<category>Adolescent Behavior</category>

</item>






<item>
<title>Post-Deployment Health Assessment in United States Service Members after Iraq Deployment: A Dissertation</title>
<link>http://escholarship.umassmed.edu/gsn_diss/16</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/gsn_diss/16</guid>
<pubDate>Mon, 21 Dec 2009 11:38:39 PST</pubDate>
<description>
	<![CDATA[
	<p>The purpose of this study was to identify health and emotional-related issues of service members after a deployment to Iraq. Secondary data analysis and a cross-sectional descriptive design, were used to analyze data from the Department of Defense Post Deployment Health Assessment (PDHA) database. The cognitive appraisal model of stress and coping (Lazarus and Folkman, 1984) guided this study. Several statistical techniques were used including: frequency distributions cross tab evaluations, factor analysis, reliability calculations, regression analysis and tests for mediation.</p>
<p>The study sample included 510, 352 service members (49,998 females, 460,349 males) with a mean age of 29 years. The sample represented all components and branches of the military. Of the total sample, 51.9% (n=264,777) saw wounded, killed or dead individuals and 22.1% (n=112,620) discharged their weapon in combat. Environmental exposures were an important source of stress. Exposures to sand and dust were the largest complaint (89.8% of the sample). Multiple physical symptoms were identified and 40% of the sample reported four or more symptoms (e.g. diarrhea, back pain, headache, fatigue). PTSD symptoms were identified in 11.8% (n = 60,200) and depressive symptoms in 26.5%, (n=123,808) of participants. Results of the study indicated that age, gender, rank, race/ethnicity, military component and branch were important predictors of emotional and health-related concerns in this sample. Appraisal variables (danger of being killed and exposure concerns) mediated the relationship between immediate (physical and depressive symptoms) and long term outcomes (health perception, PTSD symptoms) for the majority of the analyses; supporting the study hypothesis. However, length of deployment did not have a significant impact on stress-related outcomes in this study. Implications for practice, policy and future research are discussed.</p>

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</description>

<author>Sean T. Collins</author>


<category>Military Personnel</category>

<category>  Iraq War, 2003 -</category>

<category>Stress Disorders, Post-Traumatic</category>

<category>Combat Disorders</category>

<category>Adaptation, Psychological</category>

<category>Dissertations, UMMS</category>

</item>






<item>
<title>Student Nurses’ Experience of Learning with Human Patient Simulation</title>
<link>http://escholarship.umassmed.edu/gsn_diss/15</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/gsn_diss/15</guid>
<pubDate>Mon, 21 Dec 2009 11:38:38 PST</pubDate>
<description>
	<![CDATA[
	<p>Human patient simulation (HPS) has been used for over 40 years in medical education. A human patient simulator is a life-like, anatomically correct, computer driven mannequin with physiologic responses that mimic real patients. Since the introduction of computerized HPS in 2000, its use by medical and nursing students has grown exponentially. Approximately 500 nursing schools are using human patient simulators in nursing education. Researchers have suggested that using HPS can assist in reducing the gaps between theory and practice by improving critical thinking, decision making and patient outcomes. An increase in recognition of medical errors has dictated the need to improve education by allowing students and clinicians to learn in an environment that permits errors and do not put real patients in danger.</p>
<p>However, there is a dearth of research on the benefits, advantages and disadvantages of HPS as well as the learning experiences of students who used HPS in their nursing education. Therefore, the purpose of this qualitative study was to describe and analyze the learning experience of baccalaureate nursing students who used HPS during their education. Focus group interviews with HPS students were recorded and transcribed for content analysis in NVIVO, a qualitative analysis software program. The results of the analysis were categorized into four major themes: Structure, Environment, Instructor and Learning. The findings revealed that HPS students felt that structure was critical to optimize learning opportunities. Students wanted to be properly oriented to the environment of the HPS sessions, and they felt that the lack of realism of the simulators did not negatively affect their learning. Students wanted knowledgeable and competent instructors who had good interpersonal communication and interaction skills. Last, students expressed that there were benefits from acting as both the nurse and the observer during HPS. The opportunity to make mistakes without harming a patient and to experience different types of nurse-to-nurse reports were viewed as positive.</p>
<p>The findings of the study suggested that further research about student perceptions of HPS learning experiences could provide valuable information for educators and policymakers to improve the implementation of HPS in nursing and medical education.</p>

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</description>

<author>Jay Kyle Ober</author>


<category>Students, Nursing</category>

<category>Education, Nursing, Baccalaureate</category>

<category>Patient Simulation</category>

<category>Dissertations, UMMS</category>

</item>






<item>
<title>Emergency Department Nurses&apos; Experiences of Violent Acts in the Workplace</title>
<link>http://escholarship.umassmed.edu/gsn_diss/14</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/gsn_diss/14</guid>
<pubDate>Mon, 21 Dec 2009 11:38:37 PST</pubDate>
<description>
	<![CDATA[
	<p>Emergency department nurses are at high risk for violence in the workplace (Keely, 2002; Fernandez et al., 1998; Nachreiner et al., 2005; Mayer et al., 1999). It is estimated that between 52% and 82% of emergency nurses will experience physical violence and 100% of emergency department nurses will experience non-physical violence in their careers. Despite this fact, there are limited studies examining workplace violence among this vulnerable group (Fernandez et al., 1998; Levin et al., 1998). Therefore, the purpose of this qualitative descriptive study was to examine the experiences of emergency department nurses with workplace violence. Levin et al.’s (2003) Ecological Occupational Model (EOHM) was used to guide this study.</p>
<p>Four focus groups were conducted with 27 nurses who represented different types of emergency departments (rural community facility to large urban Level 1 trauma center). Results of the study suggested that the majority of participants (96%) experienced some form of work-related violence and 75% had attended at least one violence education class. The major themes of frustration and powerlessness emerged from the data. Sub themes included professional conflict while caring for violent patients, personal detachment as an emotional survival mechanisms, and feelings of victimization. Additional factors contributing to workplace violence included: personal attributes of the nurse, the workplace, and the community where the emergency department was located. These study results have potential to guide intervention development aimed at reducing workplace violence in the emergency department setting.</p>

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</description>

<author>Paul Steven MacKinnon</author>


<category>Emergency Nursing</category>

<category>Emergency Service, Hospital</category>

<category>Nurses</category>

<category>Violence</category>

<category>Workplace</category>

<category>Dissertations, UMMS</category>

</item>






<item>
<title>Emergency Nurses’ Experiences with Critical Incidents: A Dissertation</title>
<link>http://escholarship.umassmed.edu/gsn_diss/13</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/gsn_diss/13</guid>
<pubDate>Tue, 15 Sep 2009 12:51:43 PDT</pubDate>
<description>
	<![CDATA[
	<p>This qualitative descriptive research study was undertaken to describe the experiences of emergency nurses with critical incidents and identify strategies used to manage these situations in the emergency department setting. Critical incidents are events, such as death or serious injury, that cause a strong emotional reaction and may overwhelm a nurse‘s usual coping skills. Nineteen nurses who worked in one of two community-based emergency departments in Central Massachusetts were interviewed and asked to describe a critical incident they had experienced in their nursing career. Qualitative content analysis revealed two major themes: (1) critical incident experiences; and (2) aftermath; and five subthemes: (a) connections; (b) workplace culture; (c) responses; (d) lasting effects; and (e) strategies.</p>
<p>Critical incidents were limited to events with children, patient deaths, and interactions with family; this differed from prior research in that no incidents were identified involving multiple casualties, violence, or mutilating injuries. Connections occurred when the patient was known to the nurse or reminded the nurse of self or family. Responses were the reactions of the participants to the critical incident and were physical, psychological, and spiritual in nature. The majority of study participants cried in response to a critical incident. Workplace culture, a subtheme not found in other studies, involved their perceptions of expected behavior in the emergency department and emphasized the influence of workplace culture on newer or inexperienced nurses.</p>
<p>The theme of aftermath described the time period following critical incident. Lasting effects occurred in the form of vivid memories that were triggered by different stimuli. The subtheme, strategies, revealed that nurses desired, but lacked formal strategies to manage their reactions following a critical incident. Thus, they described the use of informal strategies such as talking to co-workers and family members.</p>
<p>Implications of this study support the need for educational preparation and support of emergency nurses who deal with critical incidents in the workplace. Intervening during the critical incident experience and having follow-up strategies in place to prevent distress and enhance coping in the aftermath are important for well-being, practice, and patient care in the emergency setting.</p>

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</description>

<author>Cynthia Francis Bechtel</author>


<category>Nurse’s Role</category>

<category>Emergency Nursing</category>

<category>Critical Care</category>

<category>Stress, Psychological</category>

<category>Academic Dissertations</category>

<category>Dissertations, UMMS</category>

</item>






<item>
<title>Clinical Decision Making by Critical Care Mid-Level Practitioners Working within an Interdisciplinary Team: A Dissertation</title>
<link>http://escholarship.umassmed.edu/gsn_diss/12</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/gsn_diss/12</guid>
<pubDate>Wed, 05 Aug 2009 13:03:27 PDT</pubDate>
<description>
	<![CDATA[
	<p>To improve patient safety a major change in health care reduced medical resident work hours to limit provider fatigue, in 2002 (Philibert, Friedmann, Williams, & Hours, 2002). This resulted in mid-level practitioners filling this provider void in health care teams, including critical care units (Buchanan, 1996; Christmas et al., 2005; Hoffman, Tasota, Scharfenberg, Zullo, & Donahoe, 2003; Hoffman, Tasota, Zullo, Scharfenberg, & Donahoe, 2005; Hooker & McCaig, 1996, 2001; Kaups, Parks, & Morris, 1998; Miller, Riehl, Napier, Barber, & Dabideen, 1998; Yeager, Shaw, Casavant, & Burns, 2006). In order to make appropriate clinical decisions for patients in critical care settings, mid-level practitioners are required to interpret data from multiple sources and to assimilate this information in a timely manner (Bernard, Corwin, & MacIntyre, 2000). Although these practitioners are actively involved in decision making individually and among interdisciplinary teams in critical care units, their decision making has not been described in the literature to date (Shortell et al., 1994).</p>
<p>Therefore, the purpose of this qualitative study was to describe how critical care mid-level practitioners (<em>N</em> = 17) make decisions within an interdisciplinary team, undergirded by the cognitive continuum theory. A qualitative research design using focus groups guided by naturalistic inquiry enabled data collection. An interview guide, developed from the literature review and undergirded by the cognitive continuum theory, was used to structure discussion in the focus groups. Additionally, a demographic questionnaire and vignette were used to aid in description of findings. Data was managed by note based analysis and summarized on a Microsoft Excel document. Qualitative description was used to illustrate the findings.</p>
<p>Prior to this study, there was a paucity of empirical literature describing the clinical decision making of critical care mid-level practitioners. The findings revealed a web of complexity in mid-level practitioner decision making on an interdisciplinary team. This included an overarching theme of <em>quality of care</em>, with central overlapping themes of <em>judgment</em>, <em>resources</em>, and <em>negotiation</em> interwoven with sub-themes of <em>trust</em>, <em>communication</em>, <em>experience</em>, and <em>team structure</em>. This study’s findings have direct implications for mid-level practitioner training courses, mid-level training, critical care orientation programs, theory development, and health policy.</p>

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</description>

<author>Melinda Darrigo</author>


<category>Nurse Practitioners</category>

<category>Physician Assistants</category>

<category>Decision Making</category>

<category>Interdisciplinary Communication</category>

<category>Patient Care Team</category>

<category>Academic Dissertations</category>

<category>Dissertations, UMMS</category>

</item>






<item>
<title>Women’s Knowledge of Cardiovascular Risk Factors, Level of Self-Nurturance and Participation in Heart-Healthy Behaviors: A Dissertation</title>
<link>http://escholarship.umassmed.edu/gsn_diss/11</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/gsn_diss/11</guid>
<pubDate>Wed, 05 Aug 2009 13:03:25 PDT</pubDate>
<description>
	<![CDATA[
	<p>The number one killer of women in the United States is cardiovascular disease (CVD). Cardiovascular risk factors (CVRFs) include advancing age, cigarette smoking, diabetes, dyslipidemia, family history, hypertension, obesity, sedentary lifestyle and high intake of saturated fats and low dietary fiber. A women’s risk for development of CVD dramatically increases after menopause and with the number of CVRFs. CVD is often preventable. Evidence supports addressing CVRFs reduction early (in the pre-menopausal years) through heart-healthy behaviors such as increasing physical activity, promoting healthy eating, moderate alcohol consumption and not smoking. Therefore, understanding premenopausal women’s CVRFs knowledge is an important area of inquiry. In addition, the Nemcek Wellness Model suggests that self-nurturance, as well as knowledge, may be an important factor for explaining women’s wellness behaviors. Thus, the purpose of this study was to investigate knowledge of CVRFs, level of self-nurturance and the performance of heart-healthy behaviors in women ages 35 to 55 years.</p>
<p>This study used a cross sectional survey design and venue sampling. The survey included demographic questions, the Self Nurturance Survey, the Heart Disease Facts Questionnaire, the Physical Activity Questionnaire, Prime Screen, and questions about financial strain, cigarette smoking, and alcohol use. The sample included 136 women (survey response rate = 57%), the majority of whom were white (94.9%), married (80.1%), did not smoke (80.1%) and rarely drank alcohol (57.4%).</p>
<p>Results indicated that study participants were very knowledgeable about CVRFs. (Mean knowledge score = 19.53, possible range = 0 to 25 with higher scores indicating greater knowledge). Knowledge did not predict physical activity (p = .07), diet (p = .08) or smoking status (p = .11) in this sample. Self-nurturance was moderately correlated (r = .33) with consuming a heart-healthy diet. Hypotheses derived from the Nemcek Wellness Model were not supported in this study. More research is needed to identify factors that will help women translate knowledge into heart-healthy behaviors.</p>

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</description>

<author>Annette Jakubisin Konicki</author>


<category>Cardiovascular Diseases</category>

<category>Health Behavior</category>

<category>Premenopause</category>

<category>Risk Factors</category>

<category>Primary Prevention</category>

<category>Academic Dissertations</category>

<category>Dissertations, UMMS</category>

</item>






<item>
<title>Certified Nursing Assistants’ Perceptions of Nursing Home Patient Safety Culture: Is There a Relationship to Clinical or Workforce Outcomes?: A Dissertation</title>
<link>http://escholarship.umassmed.edu/gsn_diss/10</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/gsn_diss/10</guid>
<pubDate>Mon, 14 Apr 2008 15:10:33 PDT</pubDate>
<description>
	<![CDATA[
	<p>Patient safety culture (PSC) is a critical factor in creating high   reliability healthcare organizations. However, few studies to date   have correlated PSC measures with actual safety outcomes. In   particular, nursing home studies have only recently appeared in the   literature. Nursing homes differ from hospitals in that the vast   majority of direct care is provided by certified nursing assistants   (CNAs), not licensed nurses. Thus nursing home PSC could differ in   important ways from PSC in acute care institutions.</p>
<p>This dissertation was a secondary data analysis that examined   whether CNAs’ perceptions of patient safety culture were correlated   with clinical outcomes in a random sample of 74 nursing homes in   five randomly selected states. This study matched CNA PSC survey   data using the Hospital Survey of Patient Safety Culture (HSOPSC)   with Minimum Data Set (MDS), Area Resource File (ARF) and Online   Survey Certification and Reporting (OSCAR) data from those same   homes during the first two quarters of 2005. In the original study,   1579 nurse aides out of 2872 completed the survey, for a 55%   response rate.</p>
<p>In addition to clinical outcomes, this study examined the   relationship between CNA PSC scores and staff turnover. The   relationship between certain demographic variables, such as level of   education, tenure as a CNA, and PSC scores was evaluated. The   relationship between certain facility characteristics, such as   profit status and bed occupancy was also assessed. An exploratory   factor analysis of the original HSOPSC instrument was re-run for   this nursing home CNA sample.</p>
<p>Data were analyzed using Poisson regression and multilevel   techniques; descriptive statistics were compiled for demographic   data. Major findings from the regression analyses and combined GEE   models suggest that certain factors, such as CNA turnover and LPN   staffing may predict CNA PSC scores. CNA PSC scores were associated   with rates of falls and restraint use, but were not associated with   differences in pressure ulcer rates in this sample. Few associations   for CNA PSC with individual subscales were identified. The   exploratory factor analysis revealed some potential differences in   how items and subscales factored in this nursing home CNA   population.</p>
<p>This dissertation represents an important step in the evaluation of   CNA PSC in nursing homes and the relationship of PSC to safety   outcomes. Future work on nursing home PSC and clinical and workforce   outcomes is described.</p>

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</description>

<author>Alice F. Bonner</author>


<category>Nurses’ Aides</category>

<category>Attitude of Health Personnel</category>

<category>Nursing Homes</category>

<category>  Outcome Assessment (Health Care)</category>

<category>Safety Management</category>

<category>Organizational Culture</category>

<category>Academic Dissertations</category>

<category>Dissertations, UMMS</category>

</item>






<item>
<title>Nursing Practice as Knowledge Work Within a Clinical Microsystem: A Dissertation</title>
<link>http://escholarship.umassmed.edu/gsn_diss/9</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/gsn_diss/9</guid>
<pubDate>Mon, 14 Apr 2008 15:10:31 PDT</pubDate>
<description>
	<![CDATA[
	<p>Nurses have a key role in keeping patients safe from medical errors   because they work at the point of care where most errors occur. Nursing work at   the intersection of patients and health care systems requires high levels of cognitive   activity to anticipate potential problems and effectively respond to rapidly evolving and   potentially harmful situations. The literature describes nursing work at the   intersection of patient and health care system as well as barriers to providing safe patient care. However,   little is known about the systems knowledge nurses use to negotiate the health care system on   their patients’ behalf, or how this systems information is exchanged between nurses.</p>
<p>Using the clinical microsystem as the conceptual framework, this   qualitative descriptive investigation identified and described: 1) the   components of systems knowledge needed by nurses, 2) how systems information is exchanged between   nurses, and 3) systems information exchanged between staff nurses and travel nurses. Data   were collected from a stratified maximum variation sample of 18 nurse leaders, staff   nurses, and travel nurses working within a high-functioning neonatal intensive care nursery   within a large academic medical center in New England. Data collection methods included   participant observation, document review, individual interviews, and a focus group session.   Data were analyzed through constant comparison for emerging themes   and patterns. Findings were compared for commonalities and differences within and across groups.</p>
<p>Three components of systems knowledge emerged: structural,   operational, and relational. Systems information exchange occurred through direct and   indirect means. Direct means included formal and informal mechanisms. The formal mechanism   of orientation was identified by each participant. Informal mechanisms such as peer   teaching, problem solving, and modeling behaviors were identified by participants from each of   the three nurse groups. Travel nurses’ descriptions of the common themes focused on   individual efficacy. Staff nurses focused on fostering smooth unit functioning. Nurse leaders   described common themes from a perspective of unit development. Four overarching   domains of systems information were exchanged between staff nurses and travel nurses:   practice patterns; staffing patterns and roles; tips, tricks, tidbits, and techniques;   and environmental elements. Communication emerged as a common theme across nurse groups and   domains of systems information exchanged. These findings have implications for nursing   orientation and staff development, continuous improvement at the local level, and   curriculum development.</p>

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</description>

<author>Lea R. Ayers LaFave</author>


<category>Nurses</category>

<category>Nursing Process</category>

<category>Professional Practice	Attitude of Health Personnel</category>

<category>Interprofessional Relations</category>

<category>Safety Management</category>

<category>Academic Dissertations</category>

<category>Dissertations, UMMS</category>

</item>





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