A qualitative study of the information needs of high-risk women undergoing prophylactic oophorectomy

2000 ◽  
Vol 9 (6) ◽  
pp. 486-495 ◽  
Author(s):  
N. Hallowell
Healthcare ◽  
2021 ◽  
Vol 9 (11) ◽  
pp. 1552
Author(s):  
Winifred Chinyere Ukoha ◽  
Ntombifikile Gloria Mtshali

Preconception care is biomedical, behavioural, and social health interventions provided to women and couples before conception. This service is sometimes prioritised for women at high risk for adverse pregnancy outcomes. Evidence revealed that only very few women in Africa with severe chronic conditions receive or seek preconception care advice and assessment for future pregnancy. Thus, this study aimed to explore the perceptions and practice of preconception care by healthcare workers and high-risk women in Kwa-Zulu-Natal, South Africa. This exploratory, descriptive qualitative study utilised individual in-depth interviews to collect data from 24 women at high risk of adverse pregnancy outcomes and five healthcare workers. Thematic analysis was conducted using Nvivo version 12. Five main themes that emerged from the study include participants’ views, patients’ access to information, practices, and perceived benefits of preconception care. The healthcare workers were well acquainted with the preconception care concept, but the women had inconsistent acquaintance. Both groups acknowledge the role preconception care can play in the reduction of maternal and child mortality. A recommendation is made for the healthcare workers to use the ‘One key’ reproductive life plan question as an entry point for the provision of preconception care.


2002 ◽  
Vol 87 (1) ◽  
pp. 52-56 ◽  
Author(s):  
Katherine Leeper ◽  
Rochelle Garcia ◽  
Elizabeth Swisher ◽  
Barbara Goff ◽  
Benjamin Greer ◽  
...  

Author(s):  
Sushma Rajbanshi ◽  
Mohd Noor Norhayati ◽  
Nik Hussain Nik Hazlina

Maternal and neonatal morbidity and mortality tend to decrease if referral advice during pregnancy is utilized appropriately. This study explores the reasons for nonadherence to referral advice among high-risk pregnant women. A qualitative study was conducted in Morang District, Nepal. A phenomenological inquiry was used. Fourteen participants were interviewed in-depth. High-risk women who did not comply with the referral to have a hospital birth were the study participants. Participants were chosen purposively until data saturation was achieved. The data were generated using thematic analysis. Preference of homebirth, women’s diminished autonomy and financial dependence, conditional factors, and sociocultural factors were the four major themes that hindered hospital births. Women used antenatal check-ups to reaffirm normalcy in their current pregnancies to practice homebirth. For newly-wed young women, information barriers such as not knowing where to seek healthcare existed. The poorest segments and marginalized women did not adhere to referral hospital birth advice even when present with high-risk factors in pregnancy. Multiple factors, including socioeconomic and sociocultural factors, affect women’s decision to give birth in the referral hospital. Targeted interventions for underprivileged communities and policies to increase facility-based birth rates are recommended.


2005 ◽  
Vol 96 (2) ◽  
pp. 439-443 ◽  
Author(s):  
Roelien I. Olivier ◽  
Lottie A.C. Lubsen-Brandsma ◽  
Hester van Boven ◽  
Marc van Beurden

2020 ◽  
Author(s):  
Tarsha Jones ◽  
Ashlee Guzman ◽  
Thomas Silverman ◽  
Katherine Freeman-Costin ◽  
Rita Kukafka ◽  
...  

BACKGROUND : Chemopreventive agents such as selective estrogen receptor modulators (SERMs) and aromatase inhibitors (AIs) have proven efficacy in reducing breast cancer risk by 41%-79% in high risk women. Women at high risk of developing breast cancer face the complex decision of whether to take SERMs or AIs for breast cancer chemoprevention. RealRisks, is a patient-centered web-based decision aid (DA) that was designed to promote understanding of breast cancer risk and to engage diverse women in planning a preference-sensitive course of decision-making about taking chemoprevention. OBJECTIVE We aimed to understand perceptions of women at high-risk for developing breast cancer regarding their experience using RealRisks, a DA designed to promote uptake of breast cancer chemoprevention and to understand their information needs. METHODS We completed enrollment to a randomized controlled trial (RCT) among 300 racially/ethnically diverse women at high-risk of breast cancer, who were assigned to standard educational materials alone or in combination with RealRisks. We conducted semi-structured interviews with a subset of 27 high-risk women enrolled in the intervention arm of the RCT who initially accessed the tool on average one-year prior, to understand how they interacted with the tool. All interviews were audio-recorded, transcribed verbatim, and compared against the digital audio recordings to ensure accuracy of the content. We used content analysis to generate themes. RESULTS The mean age of the 27 participants was 60.9 years (SD=10.3). Participants were 18.5% non-Hispanic black, 14.8% Hispanic/Latina, and 3.7% Asian. Most participants (78%) reported using RealRisks after being granted access to the DA. Four overarching themes emerged from the qualitative analyses: (1) acceptability of the intervention, (2) specifically endorsed elements of the DA, (3) recommendations for improvements, and (4) information needs. Most women who used RealRisks found it acceptable (n=21/27) and considered it to be helpful. Most women (n=13/21) reported that RealRisks was easy to navigate, user-friendly, and easily accessible online. The majority felt that RealRisks improved their knowledge about breast cancer risk and chemoprevention options (n=18/21), and that RealRisks informed their decision-making about whether or not to take chemoprevention (n=17/21). Some women (n=9/21) shared recommendations for improvements, as they wanted more tailoring based upon user characteristics, felt the DA was targeting a narrow population of Hispanic/Latina by using graphic novel-style narratives, wanted more understandable terminology, and felt that the tool had too strong of an emphasis on chemoprevention drugs. Participants also shared their information needs on mammography screening frequency and modifiable lifestyle factors. CONCLUSIONS This qualitative study has demonstrated the acceptability of the RealRisks web-based DA among a diverse group of high-risk women with some recommendations for improvement. These results emphasize the need for more tailoring of the DA based on user characteristics, a comprehensive approach to reducing breast cancer risk, and information needs.


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