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Development of a Family-Centered Communication Tool for Kidney Health in Premature Infants: Qualitative Focus Group
Michelle C Starr1, Samantha Wallace2, Courtney Moore3
1Division of Pediatric Nephrology, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, United States.
Insights
Caregivers of premature infants are open to discussing kidney health risks during NICU stays. Developing effective communication tools is key for long-term monitoring and adherence to care plans.
Area of Science:
- Neonatology
- Pediatric Nephrology
- Health Communication
Background:
- Premature infants face significant risks of acute kidney injury (AKI) and chronic kidney disease (CKD).
- The risk of CKD in premature infants is often underestimated by healthcare teams and caregivers.
- Effective communication strategies are crucial for ensuring proper follow-up and adherence to care for these vulnerable infants.
Purpose of the Study:
- To investigate family caregiver attitudes towards kidney health and risk communication during neonatal intensive care unit (NICU) admissions.
- To understand caregiver preferences for receiving information about the risk of CKD in premature infants.
Main Methods:
- Qualitative group sessions augmented with human-centered design methods (card sorting, projective methods, experience mapping).
- Inclusion of caregivers whose premature infants experienced AKI or other kidney complications.
- Assessment of both parent preferences and clinician perspectives.
Main Results:
- Caregivers and clinicians identified barriers and facilitators for long-term kidney monitoring and risk communication.
- Caregivers prioritized the type, depth, and timing of information delivery.
- Emphasis was placed on collaboration between hospital teams and primary care providers.
Conclusions:
- Family caregivers are receptive to discussions about kidney health during neonatal admissions.
- Future work will focus on developing and testing family-centered communication tools based on caregiver preferences.
Background:
Premature infants are at increased risk of kidney-related complications, including acute kidney injury (AKI) and chronic kidney disease (CKD). The risk of CKD in prematurely born infants is underrecognized by health care teams and caregivers. Understanding how to communicate the risk of CKD to caregivers is essential for longitudinal clinical follow-up and adherence.
Objective:
This study aimed to determine family caregiver attitudes toward kidney health and risk communication during a neonatal intensive care admission. We also sought to understand caregiver preferences for the communication of information surrounding the risk of CKD in premature infants.
Methods:
We augmented standard qualitative group sessions with human-centered design methods to assess parent preferences and clinician perspectives. Caregivers recruited had a prematurely born child who spent time in the neonatal intensive care unit at Riley Hospital for Children in Indianapolis, Indiana, and experienced AKI or another kidney complication, which put them at risk for future CKD. We used a variety of specific design methods in these sessions, including card sorting, projective methods, experience mapping, and constructive methods.
Results:
A total of 7 clinicians and 8 caregivers participated in 3 group sessions. Caregivers and clinicians readily acknowledged barriers to and drivers of long-term kidney monitoring as well as opportunities for communication of the risk of long-term kidney disease. Caregivers' primary concerns were for both the type and depth of information conveyed as well as the time at which it was communicated. Participants emphasized the importance of collaboration between the hospital care team and the primary care provider. Participant input was synthesized into several prototype concepts and, ultimately, into a rough prototype of a website and an informational flyer.
Conclusions:
Caregivers of premature infants are open to communication about kidney health during their neonatal admission. The next phase of this work will translate caregivers' preferences into family-centered communication tools and test their efficacy in the neonatal intensive care unit.
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