scholarly journals Maternal and Paternal Representations in Assisted Reproductive Technology and Spontaneous Conceiving Parents: A Longitudinal Study

2021 ◽  
Vol 12 ◽  
Author(s):  
Marcella Paterlini ◽  
Federica Andrei ◽  
Erica Neri ◽  
Elena Trombini ◽  
Sara Santi ◽  
...  

Aim of this study was to investigate whether parental mental representations during pregnancy and after delivery differed between parents who conceived after Assisted Reproductive Treatments (ART) and spontaneous conceiving (SC) parents. Effects of specific ART variables (previous ART attempts, treatment type and cause of infertility) were also taken into account. Seventeen ART couples and 25 SC couples were recruited at Santa Maria Nuova Hospital (Reggio Emilia, Italy). At both 32 weeks of gestation (T1) and 3 months postpartum (T2) participants completed the Semantic Differential of the IRMAG, a self-report tool which measures specific domains of mental representations pertaining either individual (Child, Self-as-woman/man, and Partner) or parental (Self-as-parent, Own parent) characteristics. Results showed that ART parents had significantly more positive representations of the child compared to SC parents, while the scores at Partner dimension improved from T1 to T2 for SC parents only. With regards to ART history, scores at the Self-as-woman/man dimension were significantly less positive for ICSI than IVF parents and improved substantially from T1 to T2 only in case of mothers with previous ART attempts and of fathers at the first ART cycle. The representation of own parents increased from T1 to T2 in case of infertility diagnosis due to male factors, while a decrease emerged when infertility was due to female factors. Findings suggest the need to investigate parental mental representations after ART, in order to improve the understanding on the transition to parenthood of infertile couples and to target more specific intervention for parenting support.

2021 ◽  
pp. 088626052110014
Author(s):  
Doris F. Pu ◽  
Christina M. Rodriguez ◽  
Marina D. Dimperio

Although intimate partner violence (IPV) is often conceptualized as occurring unilaterally, reciprocal or bidirectional violence is actually the most prevalent form of IPV. The current study assessed physical IPV experiences in couples and evaluated risk and protective factors that may be differentially associated with reciprocal and nonreciprocal IPV concurrently and over time. As part of a multi-wave longitudinal study, women and men reported on the frequency of their IPV perpetration and victimization three times across the transition to parenthood. Participants also reported on risk factors related to personal adjustment, psychosocial resources, attitudes toward gender role egalitarianism, and sociodemographic characteristics at each wave. Participants were classified into one of four IPV groups (reciprocal violence, male perpetrators only, female perpetrators only, and no violence) based on their self-report and based on a combined report, which incorporated both partners’ reports of IPV for a maximum estimate of violence. Women and men were analyzed separately, as both can be perpetrators and/or victims of IPV. Cross-sectional analyses using self-reported IPV data indicated that IPV groups were most consistently distinguished by their levels of couple satisfaction, across gender; psychological distress also appeared to differentiate IPV groups, although somewhat less consistently. When combined reports of IPV were used, sociodemographic risk markers (i.e., age, income, and education) in addition to couple functioning were among the most robust factors differentiating IPV groups concurrently, across gender. In longitudinal analyses, sociodemographic vulnerabilities were again among the most consistent factors differentiating subsequent IPV groups over time. Several gender differences were also found, suggesting that different risk factors (e.g., women’s social support and men’s emotion regulation abilities) may need to be targeted in interventions to identify, prevent, and treat IPV among women and men.


2021 ◽  
Vol 39 (15_suppl) ◽  
pp. e23557-e23557
Author(s):  
Jonathan R. Day ◽  
Benjamin Miller ◽  
Sarah L. Mott ◽  
Bradley T. Loeffler ◽  
Munir Tanas ◽  
...  

e23557 Background: Sarcomas are a diverse group of neoplasms that vary greatly in clinical presentation and responsiveness to treatment. Given the differences in the sites of involvement, rarity, and treatment modality, a multidisciplinary approach is required. Previous literature suggests patients with sarcoma suffer from poorer quality of life (QoL) especially physical and functional well-being. This study aims to understand if there is an association between treatment at a tertiary sarcoma center and a difference in QoL. Methods: De-identified data was obtained from the Sarcoma Tissue Repository at University of Iowa. Mixed effects regression models were utilized to evaluate the association between disease and treatment characteristics and QoL. QoL was assessed using the self-report FACT-G questionnaire at 12-, 24-, and 36-months post-diagnosis; overall scores and the 4 well-being subscales (Physical, Emotional, Social, Functional) were calculated. Results: 443 patients were identified. Soft tissue sarcomas were more prevalent (87.6%) than bone (12.4%). 53% of patients received chemotherapy and 38.6% got radiation therapy. Sarcomas were most frequently located in the lower extremities(ext.) (33.1%), followed by abdomen (20.9%), pelvic (13.6%), upper ext. (13.1%), thorax (11.3%), head & neck (7.8%). For ext. sarcoma; lower ext: 144 (71.3%), Upper ext: 58 (28.7%). Patients with extremity sarcoma; 133 had limb sparing and 48 had amputations. FACT-G Scores did not appreciably vary between 12, 24-, and 36-month for any QoL responses. Overall well-being had a mean score reported of 87.7 (sd = 15.7). Social well-being sores averaged 23.5 (5.0). Emotional well-being (EWB) 19.2 (4.1) and functional well-being (FWB) 21.3 (6.1), and physical well-being (PWB) 23.7 (4.6). There was no association between overall, PWB, EWB, or FWB with the histological subtype, radiation treatment, type of limb surgery, or any location in the same patients over time. Chemotherapy treatments were associated with lower well-being in multiple domains; PWB scores being 2.01 points lower, (p < 0.01), EWB scores being 1.27 points lower (p = 0.01) and FWB scores being 1.72 (p = 0.03), and 4.44 points lower overall (p = 0.03), on average, after adjusting for overall changes across time. Patients with ext. sarcoma only overall FACT-G scores differed 6.72 points higher for upper ext. than lower ext (p = 0.04). Conclusions: Overall QoL areas were similar to normative FACT-G scores both overall and specific areas. Having received chemotherapy was associated with lower well-being scores physically, emotionally, functionally, and overall. There were no clinically relevant differences reported in QoL scores between 12-,24-, and 36-months in the same patients. Further work is needed to describe QoL differences among patients with sarcoma at tertiary centers and examine what protective factors may influence patient well-being.


Author(s):  
Joseph Shatzmiller

This chapter briefly reviews the art history from 1230–1450 CE in order to better understand the cultural profile of the rabbi, and to evaluate the contribution of the wall paintings in his house as indications of the artistic horizons of German Jews of the fourteenth century. It also shows how Jews had to abandon the art that they cherished for generations, yet they found ways to keep alive their fascination with the beautiful and to nurse their aesthetic needs. The interior synagogue of Santa Maria la Blanca of Toledo and that of the recently reconstructed Sinagoga Mayor of Segovia manifest a profound attachment to Islamic public architecture. Jews showed great appreciation for the decorative value of their Hebrew alphabet. They also learned to paint inanimate or geometric images in miniature letters on the covers of their Bibles.


2019 ◽  
Vol 123 (3) ◽  
pp. 806-824 ◽  
Author(s):  
Alyson F. Shapiro ◽  
John M. Gottman ◽  
Brandi C. Fink

The goal of the present research was to test the efficacy of the Bringing Baby Home couple-focused psychoeducational program for promoting father involvement and related satisfaction. A randomized clinical trial design was used to randomly assign 136 pregnant couples to either an intervention or control group. Father involvement post-intervention was assessed through self-report of engagement in parenting tasks. Intent-to-treat analysis of covariance analyses indicated that fathers who participated in the Bringing Baby Home program reported significantly more involvement in parenting tasks, satisfaction with the division of parenting labor, and feeling appreciated by their wives. Both husbands and wives were also more satisfied with the division of labor when fathers were more involved in parenting. Results suggest that couple-focused psychoeducational programs can be successful for promoting father involvement.


2012 ◽  
Vol 22 (2) ◽  
pp. 363-383 ◽  
Author(s):  
Sarah J. Schoppe-Sullivan ◽  
Sarah C. Mangelsdorf

2017 ◽  
Author(s):  
Brian A. Nosek

With the rise of social cognition, use of response latency as a dependent variable has become common in social psychological research. Response latency has been used by researchers to investigate processes that are not easily testable with other methodologies, such as self-report. Response latency’s usefulness as a methodological tool is notable due to its broad application in social psychology, from research on close relationships and attribution to investigations of the self and attitudes. This paper reviews the breadth of social psychological research that has used response latency to inform about mental representations, cognitive processes, and motivational tendencies.


2020 ◽  
Author(s):  
Christopher D Petsko ◽  
Ryan Lei ◽  
Jonas R. Kunst ◽  
Emile Bruneau ◽  
Nour Kteily

Research suggests that some people, particularly those on the political right, have a tendency to blatantly dehumanize low-status groups. However, these findings have largely relied on self-report measures, which are notoriously subject to social desirability concerns. To better understand just how widely blatant forms of intergroup dehumanization might extend, the present paper leverages an unobtrusive, data-driven perceptual task to examine how U.S. respondents mentally represent ‘Americans’ vs. ‘Arabs’ (a low-status group in the U.S. that is often explicitly targeted with blatant dehumanization). Data from two reverse-correlation experiments (original N = 108; pre-registered replication N = 336) and seven rating studies (N = 2,301) suggest that U.S. respondents’ mental representations of Arabs are significantly more dehumanizing than their representations of Americans. Furthermore, analyses indicate that this phenomenon is not reducible to a general tendency for our sample to mentally represent Arabs more negatively than Americans. Finally, these findings reveal that blatantly dehumanizing representations of Arabs can be just as prevalent among individuals exhibiting low levels of explicit dehumanization (e.g., liberals) as among individuals exhibiting high levels of explicit dehumanization (e.g., conservatives)—a phenomenon into which exploratory analyses suggest liberals may have only limited awareness. Taken together, these results suggest that blatant dehumanization may be more widespread than previously recognized, and that it can persist even in the minds of those who explicitly reject it.


Author(s):  
Lucinda B. Leung ◽  
Hannah N. Ziobrowski ◽  
Victor Puac-Polanco ◽  
Robert M. Bossarte ◽  
Corey Bryant ◽  
...  

Abstract Background Physician responsiveness to patient preferences for depression treatment may improve treatment adherence and clinical outcomes. Objective To examine associations of patient treatment preferences with types of depression treatment received and treatment adherence among Veterans initiating depression treatment. Design Patient self-report surveys at treatment initiation linked to medical records. Setting Veterans Health Administration (VA) clinics nationally, 2018–2020. Participants A total of 2582 patients (76.7% male, mean age 48.7 years, 62.3% Non-Hispanic White) Main Measures Patient self-reported preferences for medication and psychotherapy on 0–10 self-anchoring visual analog scales (0=“completely unwilling”; 10=“completely willing”). Treatment receipt and adherence (refilling medications; attending 3+ psychotherapy sessions) over 3 months. Logistic regression models controlled for socio-demographics and geographic variables. Key Results More patients reported strong preferences (10/10) for psychotherapy than medication (51.2% versus 36.7%, McNemar χ21=175.3, p<0.001). A total of 32.1% of patients who preferred (7–10/10) medication and 21.8% who preferred psychotherapy did not receive these treatments. Patients who strongly preferred medication were substantially more likely to receive medication than those who had strong negative preferences (odds ratios [OR]=17.5; 95% confidence interval [CI]=12.5–24.5). Compared with patients who had strong negative psychotherapy preferences, those with strong psychotherapy preferences were about twice as likely to receive psychotherapy (OR=1.9; 95% CI=1.0–3.5). Patients who strongly preferred psychotherapy were more likely to adhere to psychotherapy than those with strong negative preferences (OR=3.3; 95% CI=1.4–7.4). Treatment preferences were not associated with medication or combined treatment adherence. Patients in primary care settings had lower odds of receiving (but not adhering to) psychotherapy than patients in specialty mental health settings. Depression severity was not associated with treatment receipt or adherence. Conclusions Mismatches between treatment preferences and treatment type received were common and associated with worse treatment adherence for psychotherapy. Future research could examine ways to decrease mismatch between patient preferences and treatments received and potential effects on patient outcomes.


Blood ◽  
2011 ◽  
Vol 118 (21) ◽  
pp. 4431-4431 ◽  
Author(s):  
Paul Jacobsen ◽  
Kendra L. Sweet ◽  
Yun-Hsiang Lee ◽  
Sara Tinsley ◽  
Jeffrey E Lancet ◽  
...  

Abstract Abstract 4431 Introduction: The use of TKIs represents a major advance in the treatment of CML over previous therapies in terms of both disease response and treatment-related morbidity. Therapeutic responses to TKIs in CML are, however, rarely equivalent to cures. In most patients, residual disease remains and treatment interruptions are often followed by recurrence. Consequently, TKI therapy will be life long for most patients. The necessity of taking an oral medication daily for life, combined with the potential for treatment interruptions to result in recurrence, points strongly to the importance of studying medication adherence in CML patients prescribed TKIs. Toward this end, the present study evaluated adherence and reasons for nonadherence among CML patients who had been receiving TKI therapy for at least six months. Method: Patients were eligible for the study if they were diagnosed with CML in the chronic phase, treated with the same TKI (imatinib, nilotinib or dasatinib) for at least six months, on the same TKI dose for the past two months, and in complete cytogenic response. They were identified by reviewing clinic records and approached to participate either via mail or during a routine clinic visit. Those who provided informed consent completed a background information form assessing demographic characteristics and a self-report questionnaire assessing rates of adherence and reasons for nonadherence in the past 30 days adapted from research on adherence to tamoxifen. Clinical data were obtained through review of medical records. Descriptive statistics were used to summarize adherence information. Chi-square tests and t-tests were performed to examine relationships between indices of adherence and demographic and clinical characteristics. The study was approved by the University of South Florida Institutional Review Board. Result: Of 68 patients asked to participate, 62 (91.2%) agreed and provided complete data. These patients (53.2% male, 46.8% female) were an average of 55 years old (range = 18 to 81). They had been diagnosed with CML an average of 4.6 years previously (range = 0.6 to 12.8 years) and had been taking imatinib (56.5%), nilotinib (30.6%), or dasatinib (12.9%) for an average of 3.1 years (range = 0.5 to 8.3 years). These patients were prescribed 1 (50%), 2 (20.7%), 3 (12.1%), 4 (15.5%), and 6 (1.7%) TKI pills per day. In the past 30 days, 4 patients (6.4%) reported taking more TKIs pills per day than prescribed and 23 patients (37.1%) reported taking fewer TKI pills per day than prescribed. Among all patients, the number of days one or more doses were missed were 1 day (12.9%), 2 to 3 days (12.9%), 4 to 6 days (6.6%) and 6 or more days (4.7%). Patients who missed a dose reported that they did so because they forgot (34.8%), chose to (47.8%), or both (17.4%). Among patients who chose to miss a dose, the most common reason was “because of how the medication makes me feel” (58.3%). Whether or not patients missed a dose in the past 30 days was not significantly related to demographic variables (i.e., age, gender, education, race, marital status, employment status, or income) or clinical variables (time since diagnosis, time on current treatment, type of TKI therapy, number of TKIs pills per day, or achievement of a complete molecular response). Conclusion: The results indicate that nonadherence to prescribed TKI therapy is common and suggest the need to develop and evaluate interventions to promote continued high adherence over time. Findings further suggest that use of reminders and routine symptom assessment and management should be included as components of a comprehensive intervention strategy. Disclosures: No relevant conflicts of interest to declare.


2012 ◽  
Vol 40 (4) ◽  
pp. 425-437 ◽  
Author(s):  
Rachel Calam ◽  
Steven Jones ◽  
Matthew R. Sanders ◽  
Robert Dempsey ◽  
Vaneeta Sadhnani

Background: Children of parents with bipolar disorder are at increased risk of disturbance. Aims: This study examined relationships between parental mood, parenting, household organization and child emotional and behavioural adjustment in families with a parent with bipolar disorder to determine areas of specific need for parenting support. Method: 48 parents were recruited through advertisements via self-help organizations. The study was conducted online. Parental mood and activity was assessed by self-report questionnaires (CES-D, ISS, MDQ and SRM); parenting was assessed using the Parenting Scale (PS). The SDQ was used to assess the parent's view of their child's emotional and behavioural difficulties. The Confusion, Hubbub and Order Scale (CHAOS) assessed household organization. Results: Parents reported high levels of difficulties across all measures and scores were above clinical cut-offs on most scales. Children were reported as showing high levels of disturbance on the SDQ, including all sub-scales. Parenting and depression scores were significantly positively correlated, as were depression, parenting and CHAOS score. Regression analyses indicated that CHAOS was the strongest predictor of Total Difficulties and Emotional Symptoms on the SDQ. Conclusions: Families are likely to benefit from interventions tailored to meet their parenting needs.


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