The impact of systemic sclerosis on women's health evaluated with an ad hoc-developed patient-reported questionnaire.

IF 1.4 Q3 RHEUMATOLOGY
Maria-Grazia Lazzaroni, Liala Moschetti, Eleonora Pedretti, Laura Andreoli, Francesca Ramazzotto, Sonia Zatti, Ilaria Galetti, Paolo Airò, Angela Tincani, Franco Franceschini
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Abstract

Objective: The impact of disease on women's health-related quality of life has become increasingly important in patients with rheumatic diseases (RDs). Systemic sclerosis (SSc) mostly affects women with a broad spectrum of clinical presentations and severity, and a variable impact on daily living. The objective of the present study was to specifically address "women's health" in systemic sclerosis patients through a dedicated questionnaire.

Methods: An anonymous self-reported questionnaire (only in Italian) was developed in collaboration with obstetricians and gynecologists and subsequently revised and approved by five patient representatives. The questionnaire was administered to SSc patients during scheduled visits in an outpatient Rheumatology SSc Clinic.

Results: Between April 2021 and March 2023, 168 patients accepted to participate; among them, 44.1% had received their SSc diagnosis during reproductive age (<45 years). The questionnaire was composed of 44 questions and included 5 sections encompassing different topics. A high rate of adherence to female cancer screening programs was recorded (86.9% for cervix and 93.6% for breast cancer), while a non-regular gynecological follow-up was observed in 36.4%, mostly in patients with more severe disease phenotype. Only 42.3% accepted to compile the Female Sexual Function Index (FSFI), which indicated a sexual dysfunction (score ⩽ 26.55) in 66.2% of patients. A worse sexual function was shown to be associated with different disease manifestations, including digital ulcers. More than 90% of patients who expressed a desire for pregnancy after diagnosis received medical pre-conception counseling and were satisfied with the information provided. In contrast, discussion about contraception occurred in 37.8% of patients who had been diagnosed during fertile age. Family planning still represents an unmet need, as 43.6% of patients did not achieve their desired family size, mainly due to concerns about their capacity to care for their children.

Conclusion: The newly developed questionnaire provides a unique opportunity to comprehensively assess the experience of women with SSc. Disease burden was shown to negatively impact sexual function and adherence to regular gynecological visits. Furthermore, receiving a diagnosis during reproductive age may increase the likelihood of a reduced family size. Clinicians who take care of women with SSc should implement these domains into routine management, thus improving the health literacy of their patients.

系统性硬化症对妇女健康的影响用一种特别开发的病人报告的问卷进行评估。
目的:在风湿病(rd)患者中,疾病对女性健康相关生活质量的影响越来越重要。系统性硬化症(SSc)主要影响女性,具有广泛的临床表现和严重程度,对日常生活的影响也各不相同。本研究的目的是通过一份专门的问卷调查,专门探讨系统性硬化症患者的“女性健康”问题。方法:与产科医生和妇科医生合作开发了一份匿名自我报告问卷(仅意大利语),随后由五名患者代表修改和批准。问卷调查是在门诊风湿病SSc诊所安排的就诊期间对SSc患者进行的。结果:在2021年4月至2023年3月期间,168名患者接受参与;其中44.1%在育龄期被诊断为SSc(结论:新开发的问卷为全面评估SSc妇女的经历提供了独特的机会。疾病负担对性功能和定期妇科就诊的依从性有负面影响。此外,在育龄期间接受诊断可能会增加缩小家庭规模的可能性。照顾SSc妇女的临床医生应将这些领域纳入日常管理,从而提高患者的健康素养。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
4.10
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