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Factors that contribute to disparities in time to acute leukemia diagnosis in young people: an in depth qualitative
Lucky Ding1, Julia E Szymczak2, Erica Evans1
1University of California San Francisco (UCSF) School of Medicine, San Francisco, CA, USA.
Insights
Delays in diagnosing pediatric leukemia are often due to non-medical factors like appointment access and financial concerns, disproportionately affecting minority families. Addressing these systemic issues in primary care is key to reducing disparities.
Area of Science:
- Pediatric Oncology
- Health Services Research
- Health Disparities
Background:
- Racial and ethnic disparities in pediatric acute leukemia outcomes are known.
- Determinants of diagnostic delays in US pediatric leukemia are understudied.
Purpose of the Study:
- Identify factors contributing to delays before pediatric leukemia diagnosis.
- Understand parental experiences with the diagnostic process.
Main Methods:
- Qualitative study using in-depth semi-structured interviews.
- Purposive sampling for diversity in race, ethnicity, income, and language.
- Analysis using inductive theory-building and constant comparative method; chart review for data complementation.
Main Results:
- Parents reported frustration when intuition conflicted with provider decisions and felt testing was delayed.
- Delays stemmed from symptom misattribution, appointment access issues, and financial barriers.
- Low-income Black and Hispanic participants disproportionately reported appointment and financial concerns.
Conclusions:
- Non-disease-related factors significantly contribute to diagnostic delays in pediatric leukemia.
- Addressing diagnostic timeliness in primary care is crucial for reducing outcome disparities.
- Systemic interventions are needed to mitigate delays and improve equity in pediatric cancer care.
Background:
Racial and ethnic disparities in outcomes for Black and Hispanic children with acute leukemia have been well documented, however little is known about the determinants of diagnostic delays in pediatric leukemia in the United States. The primary objective of this study is to identify factors contributing to delays preceding a pediatric leukemia diagnosis.
Methods:
This qualitative study utilized in-depth semi-structured interviews. Parents and/or patients within two years of receiving a new acute leukemia diagnosis were asked to reflect upon their family's experiences preceding the patient's diagnosis. Subjects were purposively sampled for maximum variation in race, ethnicity, income, and language. Interviews were analyzed using inductive theory-building and the constant comparative method to understand the process of diagnosis. Chart review was conducted to complement qualitative data.
Results:
Thirty-two interviews were conducted with a diverse population of English and Spanish speaking participants from two tertiary care pediatric cancer centers. Parents reported feeling frustrated when their intuition conflicted with providers' management decisions. Many felt laboratory testing was not performed soon enough. Additional contributors to delays included misattribution of vague symptoms to more common diagnoses, difficulties in obtaining appointments, and financial disincentives to seek urgent or emergent care. Reports of difficulty obtaining timely appointments and financial concerns were disproportionately raised among low-income Black and Hispanic participants. Comparatively, parents with prior healthcare experiences felt better able to navigate the system and advocate for additional testing at symptom onset.
Conclusions:
While there are disease-related factors contributing to delays in diagnosis, it is important to recognize there are multiple non-disease-related factors that also contribute to delays. Evidence-based approaches to reduce outcome disparities in pediatric cancer likely need to start in the primary care setting where timeliness of diagnosis can be addressed.
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