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Background <p>Sickle cell disease (SCD) increasingly requires a holistic approach. Narratives have been used to complement clinical and observational findings related to quality of life (QoL). The “Sickle Cell Anemia Narrations” project aimed to help frame the illness burden and QoL of the multi-ethnic population with SCD in Italy via a narrative approach.</p> Results <p>Twenty-one adult patients with SCD and 10 informal caregivers from seven SCD centers and two Patient Associations volunteered for this project. Researchers collected anonymous narratives and independently analyzed them through content analysis. Lack of SCD knowledge on multiple levels was found to strongly impact the illness experience independent of ethnicity. Fear of stigma at school, the challenging management of vaso-occlusive crises, and a lack of SCD knowledge at the workplace were reported. Fifty-five percent of participants reported a lack of SCD knowledge among healthcare professionals working outside the expert centers and 33% reported misdiagnosis. Caregivers highlighted the lack of coordination among territorial healthcare facilities.</p> Conclusions <p>Our findings confirm that SCD represents a critical burden for patients and caregivers and indicate that lack of SCD knowledge may bolster the barriers to care, thus revealing the urgent need to enhance awareness to foster inclusion and quality of care.</p>

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Narratives unveil knowledge and awareness-related issue, reinforcing patients’ self-identity in sickle cell disease

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年2月19日

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  • Lucia De Franceschi,
  • Carla Galvani,
  • Giovan Battista Ruffo,
  • Raffaella Colombatti,
  • Giovanna Graziadei,
  • Giovanni Palazzi,
  • Donatella Venturelli,
  • Valeria Maria Pinto,
  • Alessandra Quota,
  • Annalisa Scopinaro,
  • Raffaele Vindigni,
  • Paola Chesi,
  • Gian Luca Forni,
  • Antonia Gigante,
  • Antonietta Cappuccio,
  • Alessandra Fiorencis,
  • Francesca Begali,
  • Jacopo Ceolan,
  • Silvia Vitale,
  • Simone Villaboni,
  • Maria Giulia Marini

摘要

Background

Sickle cell disease (SCD) increasingly requires a holistic approach. Narratives have been used to complement clinical and observational findings related to quality of life (QoL). The “Sickle Cell Anemia Narrations” project aimed to help frame the illness burden and QoL of the multi-ethnic population with SCD in Italy via a narrative approach.

Results

Twenty-one adult patients with SCD and 10 informal caregivers from seven SCD centers and two Patient Associations volunteered for this project. Researchers collected anonymous narratives and independently analyzed them through content analysis. Lack of SCD knowledge on multiple levels was found to strongly impact the illness experience independent of ethnicity. Fear of stigma at school, the challenging management of vaso-occlusive crises, and a lack of SCD knowledge at the workplace were reported. Fifty-five percent of participants reported a lack of SCD knowledge among healthcare professionals working outside the expert centers and 33% reported misdiagnosis. Caregivers highlighted the lack of coordination among territorial healthcare facilities.

Conclusions

Our findings confirm that SCD represents a critical burden for patients and caregivers and indicate that lack of SCD knowledge may bolster the barriers to care, thus revealing the urgent need to enhance awareness to foster inclusion and quality of care.