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Mindfulness-Based Interventions for the Occurrence of Postpartum Depression in Elderly Primiparas.

Rui Mei, Fan Peng, Jing Xiong, Chanyuan Liu, Xiu Liu, Fang Wang, Lu Lv

Contrast media & molecular imaging August 13, 2022 DOI: 10.1155/2022/4202676 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Observational study with a nested non-randomized intervention comparison Peer reviewed
Sample size 200
Population Elderly primiparas who delivered in a single hospital between January 2016 and December 2019
Intervention Mindfulness-based intervention (MBI)
Measures Five Facet Mindfulness Questionnaire, 10-item Connor-Davidson Resilience Scale, Hamilton Depression Rating Scale, Schizophrenia Quality of Life Scale
Topics Meditation Depression
Keywords Humans Depression, postpartum Risk factors Quality of life Aged Infant, newborn Female
Key findings Education level, marital status, household monthly income per person, sex of the newborn, milk volume, sleep quality, and relationship with in-laws were identified as risk factors for postpartum depression in elderly primiparas. Among women with PPD, those who received a mindfulness-based intervention showed higher mindfulness and resilience scores and lower depression and quality-of-life scale scores than those who received no intervention.

Abstract

This study aimed to investigate the independent risk factors for the occurrence of postpartum depression (PPD) in elderly primiparas and the effect of mindfulness-based intervention (MBI) on improving the PPD. Two hundred cases of elderly primiparas who underwent delivery in our hospital from January 2016 to December 2019 were enrolled as study participants and divided into an occurrence group (n = 60) and a nonoccurrence group (n = 140) according to whether they developed PPD. The occurrence group was divided into a study group (n = 30) receiving MBI and a control group (n = 30) without any intervention. Independent risk factors influencing the occurrence of PPD were identified using univariate and multivariate logistic regression analyses. The effect of the intervention was also analyzed in the study group. Education level, marital status, household monthly income per person, sex of the newborn, milk volume, sleep quality, and relationship with in-laws were risk factors for the development of PPD. After the intervention, Five Facet Mindfulness Questionnaire scores were increased in the study group and were higher than in the control group (P < 0.05). The study group also exhibited higher 10-item Connor-Davidson Resilience Scale scores, lower Hamilton Depression Rating Scale and Schizophrenia Quality of Life Scale scores than the control group (P < 0.05). A variety of independent risk factors affected the occurrence of PPD in elderly primiparas, and MBI should be targeted clinically to reduce their negative emotions, increase psychological resilience, and improve their quality of life.

Comparable studies

Other non-randomized and open-label trials on depression, most cited first.

Study Year Design Participants
Psilocybin with psychological support for treatment-resistant depression: an open-label feasibility study. Patients with moderate-to-severe, unipolar, treatment-resistant major depression 2016 Open-label feasibility trial n = 12
Psilocybin with psychological support for treatment-resistant depression: six-month follow-up. Patients with severe, unipolar, treatment-resistant major depression 2017 Open-label trial n = 20
Quality of Acute Psychedelic Experience Predicts Therapeutic Efficacy of Psilocybin for Treatment-Resistant Depression Patients with treatment-resistant depression 2018 Clinical trial n = 20
Rapid Resolution of Suicidal Ideation After a Single Infusion of anN-Methyl-D-Aspartate Antagonist in Patients With Treatment-Resistant Major Depressive Disorder Subjects with DSM-IV-diagnosed treatment-resistant major depressive disorder 2010 Open-label trial n = 33
Antidepressant Effects of a Single Dose of Ayahuasca in Patients With Recurrent Depression Patients with recurrent depression 2015 Open-label trial n = 17

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