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A call for a trauma-informed approach during compulsory care for enduring anorexia nervosa with combined PTSD - an autoethnographic perspective.对患有创伤后应激障碍合并的持续性神经性厌食症患者进行强制治疗期间采用创伤知情方法的呼吁——一种自我民族志视角
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本文引用的文献

1
Identification and Management of Peripartum Depression.围产期抑郁症的识别与管理
Am Fam Physician. 2016 May 15;93(10):852-8.
2
Repeated depression screening during the first postpartum year.产后第一年期间的重复抑郁筛查。
Ann Fam Med. 2015 May-Jun;13(3):228-34. doi: 10.1370/afm.1777.
3
The American College of Obstetricians and Gynecologists Committee Opinion no. 630. Screening for perinatal depression.美国妇产科医师学会意见书第630号:围产期抑郁症筛查
Obstet Gynecol. 2015 May;125(5):1268-1271. doi: 10.1097/01.AOG.0000465192.34779.dc.
4
Stories of postpartum depression: exploring health constructs and help-seeking in mothers' talk.产后抑郁症的故事:在母亲的讲述中探索健康观念与求助行为
Women Health. 2014;54(4):373-87. doi: 10.1080/03630242.2014.896442.
5
Suffering in silence: reasons for not disclosing depression in primary care.默默承受痛苦:初级保健中隐瞒抑郁的原因。
Ann Fam Med. 2011 Sep-Oct;9(5):439-46. doi: 10.1370/afm.1277.
6
Incorporating recognition and management of perinatal and postpartum depression into pediatric practice.将围产期和产后抑郁的识别和管理纳入儿科实践。
Pediatrics. 2010 Nov;126(5):1032-9. doi: 10.1542/peds.2010-2348. Epub 2010 Oct 25.
7
Maternal identity negotiations among low-income women with symptoms of postpartum depression.低收入产后抑郁症状妇女的产妇身份协商。
Qual Health Res. 2011 Mar;21(3):373-85. doi: 10.1177/1049732310385123. Epub 2010 Oct 8.
8
Validation of PHQ-2 and PHQ-9 to screen for major depression in the primary care population.PHQ-2 和 PHQ-9 用于在初级保健人群中筛查重度抑郁症的验证。
Ann Fam Med. 2010 Jul-Aug;8(4):348-53. doi: 10.1370/afm.1139.
9
Suffering in silence: a qualitative meta-data-analysis of postpartum depression.默默承受:产后抑郁症的定性元数据分析
J Marital Fam Ther. 2009 Apr;35(2):145-58. doi: 10.1111/j.1752-0606.2009.00112.x.
10
Postpartum depression screening at well-child visits: validity of a 2-question screen and the PHQ-9.儿童健康检查时的产后抑郁筛查:两问题筛查法及患者健康问卷-9的有效性
Ann Fam Med. 2009 Jan-Feb;7(1):63-70. doi: 10.1370/afm.933.

产后抑郁症的自传体研究

An Autoethnographic Examination of Postpartum Depression.

机构信息

Piedmont HealthCare Family Medicine, Statesville, North Carolina

Lehigh Valley Health Network, Allentown, Pennsylvania.

出版信息

Ann Fam Med. 2017 Nov;15(6):540-545. doi: 10.1370/afm.2107.

DOI:10.1370/afm.2107
PMID:29133493
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5683866/
Abstract

PURPOSE

This article examines postpartum depression (PPD) using autoethnography to explore the stigmatization of depression and cultural expectations of motherhood. Because the personal experiences of living with PPD are often absent from primary care literature, this article uses first-person narrative and analysis of intensive mothering to explore the barriers to seeking PPD treatment, the need for increasing physician confidence and comfort using screening tools, and the impact PPD stigma has on patients and their health care.

METHODS

Autoethnography, as a relatively unfamiliar methodology in primary care, is used to illuminate individual experiences of living with PPD. The author details a series of encounters as wife, mother, and patient by narrating what it means to live with the disease. A thematic analysis of the series of first-person narratives was employed to further understand the culture of motherhood and shed light on the stigmatization of PPD.

RESULTS

Four themes emerged from the analysis revealing the pressures surrounding the cultural ideologies of intensive mothering and the stigma of mental illness: essentialism, failure, shame, and avoidance.

DISCUSSION

There is a need to reframe cultural perceptions of motherhood and PPD to positively impact familial interactions and health care encounters for those who live with the illness. The article calls for providing broader diagnostic efforts, more comprehensive care, and engagement with patients in shared decision making around the diagnosis and treatment of PPD.

摘要

目的

本文通过自传体民族志研究产后抑郁症(PPD),探讨抑郁症的污名化和母性的文化期望。由于 PPD 的个人患病经历在初级保健文献中经常缺失,本文使用第一人称叙述和密集育母分析,探讨了寻求 PPD 治疗的障碍、增加医生使用筛查工具的信心和舒适度的需求,以及 PPD 污名对患者及其健康的影响。

方法

自传体民族志作为初级保健中一种相对陌生的方法,用于阐明个人 PPD 患病经历。作者通过叙述作为妻子、母亲和患者的一系列经历,详细描述了密集育母文化下的个人经历。对一系列第一人称叙述进行主题分析,以进一步了解母性文化,并揭示 PPD 的污名化。

结果

分析中出现了四个主题,揭示了密集育母文化理念和精神疾病污名化所带来的压力:本质主义、失败、羞耻和回避。

讨论

需要重新构建对母性和 PPD 的文化观念,以积极影响那些患有这种疾病的人的家庭互动和医疗保健体验。本文呼吁提供更广泛的诊断努力、更全面的护理,并在 PPD 的诊断和治疗方面与患者共同做出决策。