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Cross-Sectional Analysis of Patient-Centered Language Use in Journals Publishing Research Focused on Heart Failure. 心衰期刊发表研究中以患者为中心的语言使用横断面分析
IF 1.7 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2021-07-19 eCollection Date: 2021-01-01 DOI: 10.17294/2330-0698.1821
Vivian Pham, Benjamin Greiner, Ryan Ottwell, Matt Vassar, Micah Hartwell

Purpose: Detrimental effects of using non-patient-centered language (nPCL) have been reported for diabetes, mental illness, and obesity, and both the American Medical Association (AMA) and International Committee of Medical Journal Editors (ICMJE) recommend using patient-centered language in medical literature. Heart failure is a common yet stigmatized disease, and nPCL may further propagate stigma. This study analyzed current use of nPCL in journals focused on heart failure research and also examined whether the journals steer authors to adhere to AMA or ICMJE guidelines regarding nPCL.

Methods: Following systematic search of PubMed for heart failure-related articles published from May 1, 2018, to April 30, 2020, cross-sectional analysis was performed. Each selected article was inspected for an array of nPCL terms and frequency of nPCL usage. Chi-squared tests and multivariable logistic regressions were used to assess relationships between study characteristics and nPCL use.

Results: Of the 195 articles fully analyzed, 108 (55.4%) contained a nPCL term, the most frequently used being "heart failure patient" (78.7%), "burden" (23.1%), and "suffer" (15.7%). Use of nPCL was disproportionately more common in original research articles (63.5%) and less common in case reports (18.2%). Articles that did not detail any treatment or intervention used the most nPCL (71.1%). No statistically significant association was found between a journal's impact factor and its adherence to AMA or ICMJE recommendations.

Conclusions: nPCL is widely used in publications reporting on heart failure. We encourage authors and journals to reduce nPCL to help decrease the stigma patients with this disease often encounter.

目的:使用非以患者为中心的语言(nPCL)对糖尿病、精神疾病和肥胖的有害影响已被报道,美国医学协会(AMA)和国际医学杂志编辑委员会(ICMJE)都建议在医学文献中使用以患者为中心的语言。心力衰竭是一种常见但被污名化的疾病,而nPCL可能进一步传播污名化。本研究分析了目前nPCL在心力衰竭研究期刊上的使用情况,并检查了这些期刊是否引导作者遵守AMA或ICMJE关于nPCL的指南。方法:系统检索PubMed 2018年5月1日至2020年4月30日发表的心力衰竭相关文章,进行横断面分析。每个选定的文章都检查了一系列nPCL术语和nPCL使用频率。采用卡方检验和多变量logistic回归来评估研究特征与nPCL使用之间的关系。结果:在195篇文献中,108篇(55.4%)包含nPCL术语,使用频率最高的是“心力衰竭患者”(78.7%)、“负担”(23.1%)和“受苦”(15.7%)。nPCL在原创研究文章中的使用比例更高(63.5%),在病例报告中的使用比例更低(18.2%)。没有详细说明任何治疗或干预措施的文章使用了最多的nPCL(71.1%)。期刊的影响因子与其对AMA或ICMJE建议的依从性之间没有统计学上的显著关联。结论:nPCL在心力衰竭的报道中被广泛使用。我们鼓励作者和期刊减少nPCL,以帮助减少患有这种疾病的患者经常遇到的耻辱。
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引用次数: 4
The Weight of a Word. 一个词的分量
IF 1.7 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2021-07-19 eCollection Date: 2021-01-01 DOI: 10.17294/2330-0698.1879
Dennis J Baumgardner
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引用次数: 0
Loneliness in Primary Care Patients: Relationships With Body Mass Index and Health Care Utilization. 初级保健患者的孤独感:与体重指数和卫生保健利用的关系。
IF 1.7 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2021-07-19 eCollection Date: 2021-01-01 DOI: 10.17294/2330-0698.1808
Tamara K Oser, Siddhartha Roy, Jessica Parascando, Rebecca Mullen, Julie Radico, Alexis Reedy-Cooper, Jennifer Moss

Purpose: Rates of loneliness and obesity have increased in recent decades. Loneliness and obesity independently have been found to be risk factors for negative physical and mental health outcomes. This study examined the rates and interrelationships of loneliness, body mass index (BMI), and health care utilization in a primary care setting.

Methods: A cross-sectional survey of adult patients presenting for outpatient care at 7 family medicine clinical practices in Pennsylvania was conducted. Survey questions included self-reported measures of loneliness, height/weight, number of health care visits, and potential confounders (eg, sociodemographic variables, health status). Bivariate and multivariable linear regression models were used to analyze associations among loneliness, BMI, and health care utilization.

Results: In all, 464 eligible patients returned surveys for an overall response rate of 26%. Mean (standard deviation) loneliness score was 4.2 (1.7), mean BMI was 30.4 (7.6), and mean number of visits in year prior was 2.7 (3.6). On bivariate analysis, BMI was positively associated with loneliness (effect estimate: 0.50; P=0.03). On multivariable analysis, BMI was negatively associated with attending religious services and self-reported physical health and positively associated with self-reported mental health (P<0.05 for all), but not associated with loneliness. While not associated with loneliness, health care utilization was negatively associated with Hispanic ethnicity, marital status, and self-reported physical health (P<0.05 for all).

Conclusions: Given the detrimental effects loneliness and obesity have on health outcomes, it might be prudent for health care providers to prioritize health concerns for their patients by assessing loneliness and counseling regarding associated risks, particularly in patients with obesity.

目的:近几十年来,孤独和肥胖的比例有所上升。孤独和肥胖分别被发现是负面身心健康结果的危险因素。本研究考察了孤独感、身体质量指数(BMI)和初级保健机构医疗保健利用的比率和相互关系。方法:对宾夕法尼亚州7家家庭医学诊所门诊就诊的成年患者进行横断面调查。调查问题包括自我报告的孤独感、身高/体重、就诊次数和潜在的混杂因素(如社会人口变量、健康状况)。采用双变量和多变量线性回归模型分析孤独感、BMI和医疗保健利用之间的关系。结果:总共有464名符合条件的患者返回调查,总有效率为26%。平均(标准差)孤独评分为4.2(1.7),平均BMI为30.4(7.6),前一年平均就诊次数为2.7(3.6)。在双变量分析中,BMI与孤独感呈正相关(效应估计:0.50;P = 0.03)。在多变量分析中,BMI与参加宗教服务和自我报告的身体健康呈负相关,与自我报告的心理健康呈正相关(p结论:考虑到孤独和肥胖对健康结果的有害影响,卫生保健提供者通过评估孤独和相关风险咨询来优先考虑患者的健康问题可能是谨慎的,特别是在肥胖患者中。
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引用次数: 4
Perioperative Family Updates Reduce Anxiety and Improve Satisfaction: A Randomized Controlled Trial. 围手术期家庭更新减少焦虑并提高满意度:一项随机对照试验。
IF 1.7 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2021-04-19 DOI: 10.17294/2330-0698.1805
Lindsay S Howe, Dan Wigmore, Nathaniel J. Nelms, P. Schottel, C. Bartlett, D. Halsey, M. Krag, David J. Lunardini, R. Monsey, B. Beynnon, M. Blankstein
PurposeThis study aimed to determine if standardized updates at specific perioperative events affect anxiety and satisfaction of the family members and if the length of surgical procedure affects the satisfaction with updates.MethodsThis study was a randomized control trial. In the control group, surgeons communicated with the family only once near the completion of the procedure. In the intervention group, families received electronic updates at 3 significant perioperative events during the procedure. A postoperative survey rating family member satisfaction and anxiety levels, using a Likert scale of 0-5, was administered.ResultsMean level of overall satisfaction did not differ between groups (intervention: 4.68 ± 0.69 [95% CI: 4.50, 4.87]; control: 4.61 ± 0.78 [95% CI: 4.40, 4.82]; P=0.69). Mean anxiety levels were lower in the intervention group (2.48 ± 1.43 [2.10, 2.86]) than in the control group (3.12 ± 1.32 [2.77, 3.47]; P=0.01). Mean satisfaction with perioperative updates was higher in the intervention (4.48 ± 0.83 [4.26, 4.70]) versus control group (3.16 ± 1.89 [2.67, 3.65]; P=0.0001). For all subjects, there was positive correlation between procedure time and anxiety (Spearman's rho: 0.34; P=0.0002) and negative correlation between procedure time and overall satisfaction (Spearman's rho: -0.23; P=0.01).ConclusionsAnxiety and satisfaction with perioperative updates were significantly improved by additional perioperative updates. These findings indicate that updating families during significant standardized strategic perioperative events can reduce the anxiety of loved ones and are preferred by most families.
目的本研究旨在确定特定围手术期事件的标准化更新是否会影响家庭成员的焦虑和满意度,以及手术时间是否会影响更新的满意度。方法采用随机对照试验。在对照组中,外科医生在手术接近完成时只与家人交流过一次。在干预组中,家庭在手术期间收到了3个重要围手术期事件的电子更新。采用Likert量表0-5对家庭成员的满意度和焦虑程度进行了术后调查。结果各组的平均总体满意度无差异(干预组:4.68±0.69[95%CI:4.50,4.87];对照组:4.61±0.78[95%CI=4.40,4.82];P=0.069)。干预组的平均焦虑水平(2.48±1.43[2.10,2.86])低于对照组(3.12±1.32[2.77,3.47];P=0.01)(4.48±0.83[4.26,4.70])与对照组(3.16±1.89[2.67,3.65];P=0.0001),手术时间与焦虑呈正相关(Spearman’s rho:0.34;P=0.0002),手术时间与总体满意度呈负相关(Speerman’s rho:0.23;P=0.001)。这些发现表明,在重要的标准化策略围手术期事件中更新家庭信息可以减少亲人的焦虑,是大多数家庭的首选。
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引用次数: 7
Prevalence of Common Disease Conditions in a Large Cohort of Individuals With Down Syndrome in the United States. 在美国唐氏综合症人群中常见疾病的患病率
IF 1.7 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2021-04-19 eCollection Date: 2021-01-01 DOI: 10.17294/2330-0698.1824
Brian Chicoine, Anne Rivelli, Veronica Fitzpatrick, Laura Chicoine, Gengjie Jia, Andrey Rzhetsky

Purpose: Given the current life expectancy and number of individuals living with Down syndrome (DS), it is important to learn common occurrences of disease conditions across the developmental lifespan. This study analyzed data from a large cohort of individuals with DS in an effort to better understand these disease conditions, inform future screening practices, tailor medical care guidelines, and improve utilization of health care resources.

Methods: This retrospective, descriptive study incorporated up to 28 years of data, compiled from 6078 individuals with DS and 30,326 controls matched on age and sex. Data were abstracted from electronic medical records within a large Midwestern health system.

Results: In general, individuals with DS experienced higher prevalence of testicular cancer, leukemias, moyamoya disease, mental health conditions, bronchitis and pneumonia, gastrointestinal conditions, thyroid disorder, neurological conditions, atlantoaxial subluxation, osteoporosis, dysphagia, diseases of the eyes/adnexa and of the ears/mastoid process, and sleep apnea, relative to matched controls. Individuals with DS experienced lower prevalence of solid tumors, heart disease conditions, sexually transmitted diseases, HIV, influenza, sinusitis, urinary tract infections, and diabetes. Similar rates of prevalence were seen for lymphomas, skin melanomas, stroke, acute myocardial infarction, hepatitis, cellulitis, and osteoarthritis.

Conclusions: While it is challenging to draw a widespread conclusion about comorbidities in individuals with Down syndrome, it is safe to conclude that care for individuals with DS should not automatically mirror screening, prevention, or treatment guidelines for the general U.S. population. Rather, care for those with DS should reflect the unique needs and common comorbidities of this population.

目的:考虑到目前的预期寿命和唐氏综合征(DS)患者的数量,了解唐氏综合征在整个发育生命周期中常见的疾病状况是很重要的。本研究分析了大量DS患者的数据,以更好地了解这些疾病状况,为未来的筛查实践提供信息,制定医疗保健指南,并提高医疗保健资源的利用率。方法:这项回顾性描述性研究纳入了长达28年的数据,这些数据来自6078名DS患者和30326名年龄和性别匹配的对照组。数据是从中西部一个大型卫生系统的电子病历中提取的。结果:总体而言,与对照组相比,退行性椎体滑移患者的睾丸癌、白血病、烟雾病、精神健康状况、支气管炎和肺炎、胃肠道疾病、甲状腺疾病、神经系统疾病、寰枢半脱位、骨质疏松症、吞咽困难、眼睛/附件疾病、耳朵/乳突疾病和睡眠呼吸暂停的患病率更高。患有退行性椎体滑移的个体患实体瘤、心脏病、性传播疾病、艾滋病毒、流感、鼻窦炎、尿路感染和糖尿病的几率较低。淋巴瘤、皮肤黑色素瘤、中风、急性心肌梗死、肝炎、蜂窝织炎和骨关节炎的患病率也相似。结论:虽然对唐氏综合症患者的合并症得出一个广泛的结论是具有挑战性的,但可以肯定的是,对唐氏综合症患者的护理不应该自动反映美国普通人群的筛查、预防或治疗指南。相反,对退行性痴呆患者的护理应反映这一人群的独特需求和常见合并症。
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引用次数: 26
Assessing the Patient-Perceived Monetary Value of Patient-Reported Outcome Improvement for Patients With Chronic Knee Conditions. 评估慢性膝关节疾病患者报告预后改善的患者感知货币价值。
IF 1.7 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2021-04-19 DOI: 10.17294/2330-0698.1803
S. Floyd, A. Oostdyk, M. Cozad, John Brooks, P. Siffri, Brian Burnikel
PurposeThe high cost of orthopaedic care has attracted criticism in the current value-based health care environment. The objective of this work was to assess the properties of a willingness to pay (WTP)-based approach to estimate the monetary value that patients place on health improvements in chronic knee conditions following orthopaedic treatment.MethodsA sample of patients with a chronic knee condition were surveyed between January and May of 2018 at a large orthopaedic practice. Each patient provided their WTP for restoration to ideal knee health and completed the Single Assessment Numerical Evaluation (SANE) to describe their baseline knee state. Average WTP was calculated for the total sample and stratified by income, age, and baseline SANE (for which 0 is the worst and 100 is the best) levels. The patient-perceived monetary value of each unit of SANE improvement was assessed.ResultsThe study sample included 86 patients seeking orthopaedic care for a chronic knee condition. Mean baseline SANE score was 45.5 (standard deviation: 25.0). Mean WTP to obtain ideal knee function from baseline was $18,704 (standard deviation: $18,040). For the full sample, patients valued a 1-unit improvement in SANE score at $291.1 (β: 291.1; P<0.05). The amount of money patients were willing to pay to achieve ideal knee function varied with age, income, and baseline knee state.ConclusionsPatients appear to highly value improvement in chronic knee conditions. Willingness-to-pay survey results appear to track expected variation in patient outcome valuation by income and baseline knee condition and could be a valuable approach to assess value-based care in orthopaedics.
目的在当前以价值为基础的医疗环境下,骨科护理的高成本引起了人们的批评。本研究的目的是评估基于支付意愿(WTP)的方法的性质,以估计患者在骨科治疗后对慢性膝关节疾病健康改善的货币价值。方法对2018年1月至5月在一家大型骨科诊所就诊的慢性膝关节疾病患者进行调查。每位患者提供他们的WTP以恢复理想的膝关节健康,并完成单一评估数值评估(SANE)来描述他们的基线膝关节状态。计算总样本的平均WTP,并按收入、年龄和基线SANE(其中0为最差,100为最好)水平分层。评估患者感知的每单位SANE改善的货币价值。结果研究样本包括86例因慢性膝关节疾病寻求骨科治疗的患者。平均基线SANE评分为45.5(标准差:25.0)。从基线获得理想膝关节功能的平均WTP为18,704美元(标准差:18,040美元)。对于整个样本,患者对SANE评分改善1个单位的评价为291.1美元(β: 291.1;P < 0.05)。患者为获得理想的膝关节功能而愿意支付的费用因年龄、收入和基线膝关节状态而异。结论患者对慢性膝关节疾病的改善表现出高度重视。支付意愿调查结果似乎跟踪了收入和基线膝关节状况对患者预后评估的预期变化,可能是评估骨科中基于价值的护理的有价值的方法。
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引用次数: 1
Supply, Demand, and Quality: A Three-Pronged Approach to Blood Product Management in Developing Countries. 供应、需求和质量:发展中国家血液制品管理的三管齐下方法。
IF 1.7 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2021-04-19 DOI: 10.17294/2330-0698.1799
Kyle L. Gress, Karina Charipova, Ivan Urits, Omar Viswanath, A. Kaye
While transfusion of blood and blood products is instinctively linked to the provision of emergent care, blood and blood products are also routinely used for the treatment of subacute and chronic conditions. Despite the efforts of the World Health Organization and others, developing countries are faced with a three-part problem when it comes to access to and delivery of transfusions: insufficient supply, excessive demand, and inadequate quality of available supply. Developing countries rely heavily on replacement and remunerated donors rather than voluntary nonremunerated donors due to concerns regarding donation- and transfusion-transmitted infection as well as local and cultural beliefs. While increased awareness of HIV and improved testing techniques have jointly reduced infection-related apprehensions and improved the quality of available blood and blood products, continued efforts are warranted to bolster testing for other bloodborne pathogens. Similarly, although prevalence rates of anemia are high in some areas of the world, success in adequate widespread management of these conditions has been limited. One of the keys to expanding access to high-quality blood and blood products is thus to improve medical management of conditions that would otherwise require transfusion. Through a three-pronged approach to address quantity, quality, and demand, developing countries can enable themselves to build toward self-sufficient blood management services and increased independence from the support of international organizations.
虽然血液和血液制品的输血本能地与提供紧急护理联系在一起,但血液和血液制品也经常用于治疗亚急性和慢性疾病。尽管世界卫生组织和其他方面作出了努力,但发展中国家在获得和提供输血方面面临着一个三方面的问题:供应不足、需求过度和现有供应质量不足。由于对捐赠和输血传播感染以及当地和文化信仰的担忧,发展中国家严重依赖替代献血者和有偿献血者,而不是自愿无偿献血者。虽然提高对艾滋病毒的认识和改进检测技术共同减少了与感染有关的担忧,并提高了可用血液和血液制品的质量,但仍有必要继续努力加强对其他血源性病原体的检测。同样,虽然世界上一些地区的贫血患病率很高,但在适当的广泛管理这些疾病方面取得的成功有限。因此,扩大获得高质量血液和血液制品的关键之一是改善对需要输血的病症的医疗管理。通过解决数量、质量和需求的三管齐下的方法,发展中国家可以使自己能够建立自给自足的血液管理服务,并增加独立于国际组织的支持。
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引用次数: 3
Building Community-Engaged Multidisciplinary Partnerships to Improve Medication Management in Elderly Patients With Multiple Chronic Conditions. 建立社区参与的多学科合作伙伴关系以改善老年多重慢性病患者的用药管理。
IF 1.7 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2021-04-19 DOI: 10.17294/2330-0698.1778
I. Poon, Felicia Skelton, Lena R. Bean, Dominique Guinn, Terica L Jemerson, Ngozi D. Mbue, Creaque V Charles, U. A. Ndefo
PurposeMany studies in preventing adverse drug events have been researcher-driven, yet few have engaged patients in the development of a project. This project aims to engage minority elderly patients with multiple chronic conditions in the development of research questions and strategies to improve medication safety.MethodsElderly patients (≥65 years old) who were prescribed 7 or more chronic medications were recruited through a university-based aging resource network in a historically African American community in Houston, Texas. Patients and a caregiver participated in a multidisciplinary workgroup comprised of a physician, pharmacists, a nurse, health educators, and a social worker. Patients were engaged by utilizing the 4 patient-centered outcomes research engagement principles. The workgroup created a strategic plan, completed an environmental scan, identified research problems, and reviewed current evidence-based approaches in the literature. Workgroup findings were presented to a broader audience within a community town hall setting, and input was collected from a community-wide survey.ResultsFrom April 2018 to July 2018, 3 patients and 1 caregiver participated in 5 multidisciplinary workgroup meetings. A total of 74 seniors attended the town hall meeting, and 69 completed the surveys. The most common drug-related problems among survey participants were doubts about drug advertisements (79%) and drug interactions (70%). Most participants (88%) were more comfortable in receiving face-to-face counseling compared to an app or virtual visits. Findings aided in developing 3 grant proposals.ConclusionsThis narrative provides a roadmap for conducting multidisciplinary, patient-centered participatory research to refine research strategies in minimizing drug-related problems.
目的许多预防药物不良事件的研究都是由研究人员推动的,但很少有患者参与项目的开发。该项目旨在让患有多种慢性病的少数民族老年患者参与研究问题和策略的制定,以提高药物安全性。方法通过德克萨斯州休斯顿一个历史悠久的非裔美国人社区的大学老龄资源网络招募接受7种或7种以上慢性药物治疗的老年患者(≥65岁)。患者和护理人员参加了一个由医生、药剂师、护士、健康教育工作者和社会工作者组成的多学科工作组。采用4项以患者为中心的结果研究参与原则对患者进行参与。该工作组制定了一项战略计划,完成了环境扫描,确定了研究问题,并审查了文献中当前的循证方法。工作组的调查结果在社区市政厅环境中向更广泛的受众介绍,并从社区范围的调查中收集意见。结果2018年4月至2018年7月,3名患者和1名护理人员参加了5次多学科工作组会议。共有74名老年人参加了市政厅会议,69人完成了调查。调查参与者中最常见的毒品相关问题是对药物广告(79%)和药物相互作用(70%)的怀疑。与应用程序或虚拟访问相比,大多数参与者(88%)更愿意接受面对面的咨询。调查结果有助于制定3项赠款提案。结论该叙述为开展多学科、以患者为中心的参与性研究提供了路线图,以完善研究策略,最大限度地减少毒品相关问题。
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引用次数: 4
Musings on Patient Willingness to Pay. 关于病人支付意愿的思考。
IF 1.7 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2021-04-19 eCollection Date: 2021-01-01
Dennis J Baumgardner
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引用次数: 0
A Patient-Centered Study Examining Self-Identification of Mental Health Challenges Among Female Military Officers. 一项以患者为中心的研究,研究女性军官对心理健康挑战的自我认同。
IF 1.7 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2021-04-19 DOI: 10.17294/2330-0698.1776
Rosellen Roche, J. Manzi, Katelyn Bard
Due to the expansion of leadership roles in the military for women, female military personnel now face stressors equal to, and yet unique from, their male counterparts. This pilot study surveyed 73 female U.S. Army officers regarding their experiences of leadership and mental wellness within the military. A mixed-methods survey was distributed via 2 private Facebook groups for female Army officers following an anonymized convenience sampling. This anonymous, patient-centered protocol was used to protect against known stigma surrounding disclosing mental health concerns in the military. Respondents were asked a series of questions including perceived mental health status and access to behavioral health services. Most respondents reported feelings of stress related to their roles as officers (86.6%). Self-reported feelings of anxiety (83.6%) and depression (65.7%) were high. In contrast, only 30.1% had ever received a formal diagnosis of anxiety or depression by a mental health professional. Our survey confirmed a large percentage, 65.7% of respondents, reported avoiding mental/behavioral health services. Female military officers are able to recognize their feelings as symptoms of anxiety and depression; however, many take active steps to hide these symptoms from their family members and senior officers and avoid seeking professional care.
由于女性在军队中的领导作用扩大,女性军事人员现在面临着与男性同等但又独特的压力。这项试点研究调查了73名美国陆军女性军官,了解她们在军队中的领导经验和心理健康状况。在匿名便利抽样后,通过两个私人脸书群组为女性陆军军官分发了一份混合方法调查。这种匿名的、以患者为中心的协议被用来防止在军队中公开心理健康问题的已知污名。受访者被问及一系列问题,包括感知的心理健康状况和获得行为健康服务的机会。大多数受访者报告与他们作为军官的角色有关的压力感(86.6%)。自我报告的焦虑感(83.6%)和抑郁感(65.7%)较高。相比之下,只有30.1%的人曾被心理健康专家正式诊断为焦虑或抑郁。我们的调查证实,65.7%的受访者表示避免心理/行为健康服务。女性军官能够将自己的感受视为焦虑和抑郁的症状;然而,许多人采取积极措施,向家人和高级官员隐瞒这些症状,并避免寻求专业护理。
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引用次数: 0
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