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T. Hoveling

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10 records found

Journal article (2026) - Tamara Hoveling, Jelle Ijzenbrandt, Saba Hinrichs-Krapels, Linda Ritzen, Wichor M. Bramer, Erik van Raaij, Jeremy Faludi, Conny Bakker, Jan Carel Diehl
Background
The healthcare sector contributes substantially to environmental pollution, affecting ecosystems and public health. Circular economy (CE) strategies offer potential solutions, but existing frameworks provide limited guidance for healthcare, overlooking factors such as infection control, decontamination, and staff workload.

Methods
We developed the Circular Healthcare Flows visual, a taxonomy of CE strategies for medical devices, using observations in sterilization departments, recycling facilities, and manufacturing plants; 21 expert interviews; and a systematic review of 1104 studies (68 full-text reviews). Additional stakeholder feedback validated and refined the taxonomy.

Findings
The taxonomy identifies 13 CE strategies—refuse, replace, rethink, reduce, reuse, maintain, repair, refurbish, remanufacture, repurpose, recycle, renew, and recover—and organizes them in a healthcare-specific framework. Iterative feedback ensured that the taxonomy is clear, practically applicable, and addresses sector-specific regulatory, clinical, and operational constraints.

Interpretation
The Circular Healthcare Flows visual provides a practical tool to standardize terminology and guide the implementation of CE strategies in healthcare. By offering conceptual structure and actionable guidance, it supports informed decision-making, facilitates collaboration among stakeholders, and encourages consistent application of circular strategies across the sector.

Funding
IJzenbrandt was partially funded by Erasmus University Rotterdam and the Health and Technology Convergence Alliance of TU Delft, Erasmus MC, and Erasmus University Rotterdam. Hoveling was funded through the DiCE project (EU grant agreement no. 101060184). Opinions expressed are those of the authors and do not necessarily reflect those of the EU or REA. ...
Journal article (2026) - Tamara Hoveling, Naomi Muindi, Jeremy Faludi, Conny Bakker
This study explores how circular design principles can be applied to single-use laparoscopic staplers to improve their carbon footprint without compromising critical requirements such as safety, performance, and financial feasibility. Using a research-through-design approach, four alternative concepts were developed: a fully recyclable device, a partially reusable device, a multifunctional device, and a manual device, aiming to reduce the carbon footprint while maintaining clinical performance of the device. Iterative design cycles incorporated feedback from Medtech professionals and from qualitative surveys with additional industry stakeholders. Fast-track life cycle assessments (LCAs) estimated environmental impact compared to the baseline device, while stakeholder feedback assessed trade-offs and synergies related to safety, usability, workflow compatibility, and regulatory compliance. Here, “trade-offs” refer to improvements in circularity coming with losses in other requirements, while “synergies” improve both circularity and other requirements together. Results revealed that each concept delivered potential carbon footprint reductions, particularly the reusable, multifunctional, and manual variants. Trade-offs included increased sterilization burden, altered surgical workflow, and reduced user familiarity; synergies included lower material and logistics costs from reuse and multifunctional design, achieved without compromising safety or usability. The findings highlight that achieving circularity in medical device design involves more than technical considerations; it requires a systems-level approach. Effective implementation depends on aligning design strategies with regulatory requirements, clinical workflows, and supply chain practices. This study provides recommendations to navigate trade-offs and identify synergies, supporting a structured approach to advancing sustainable practices in healthcare. ...

Designing Medical Devices for a Circular Economy

Doctoral thesis (2026) - Tamara Hoveling, C.A. Bakker, J. Faludi
Climate change is widely recognized as the greatest threat to human health, yet healthcare itself contributes significantly to environmental harm. Environmental pressures beyond climate change, such as the encroachment on wild lands that increases pandemic risks and the growing demand for scarce resources used in modern technologies, also contribute to these health risks. Despite these challenges, many high-tech solutions continue to rely on scarce materials but are used only briefly, and an increasing number of products are designed to be disposable. Single-use items, whether packaging, medical disposables, or complex electronic devices, are often discarded after minimal patient contact, as this is perceived to maximize safety.

A particular challenge within this context is posed by medical devices containing electronic components. These devices depend on critical raw materials and energy-intensive production processes and are composed of complex multi-material assemblies. At end of life, their disposal raises environmental concerns, as collection and recycling systems achieve only partial material recovery, while improper treatment of electronic waste can release hazardous substances into the environment. Together with rapid technological development and strict regulatory requirements, these factors complicate the application of circular approaches in design. This dissertation examines not only why this is the case, but also how it can be improved.

The central research question of this dissertation is therefore:
How can medical devices containing electronic components be redesigned to support a circular economy while ensuring clinical and regulatory compliance?

To answer this question, the dissertation is structured in five parts. Part I introduces the problem, exploring healthcare’s environmental impact, medical device design challenges, and the rationale for circular economy principles. Part II investigates the current state of medical device design through literature review and qualitative methods, identifying barriers and opportunities for circularity and clarifying how stakeholders can collaborate effectively. It also presents the Circular Healthcare Flows visual taxonomy, which shows how R-strategies can be implemented and maps how materials, components, and devices can circulate within clinical, regulatory, and operational contexts, providing a shared language and conceptual clarity for designers, clinicians, and policymakers. Part III presents two design case studies, demonstrating practical application of circular economy principles and highlighting trade-offs, integration challenges, and strategies to overcome them. Part IV translates these insights into practical approaches, forming the foundation for a Circular Design Guide. Finally, Part V discusses lessons learned, reflections, and directions for future research.

The research shows that circular strategies in healthcare are possible but context dependent. Analysis of over 1,400 medical devices revealed that while some devices incorporate reuse, most remain single use. Barriers are not only technological—they stem from regulations, institutional practices, and risk perceptions, while inconsistent terminology and concepts complicate coordination across stakeholders. The visual taxonomy helps address this conceptual ambiguity, enabling stakeholders to align on terminology, understand circular flows, and make context-sensitive decisions.

Design experiments illustrated how insights can be applied. Mid-level R-strategies such as reuse, repair, and refurbishment provide tangible environmental benefits without disrupting clinical workflows. Broader strategies, such as refuse, rethink, and reduce, offer greater impact but require reconsidering device use and care delivery. Trade-offs between circularity, safety, usability, and compliance can be navigated—and sometimes leveraged—through careful design, stakeholder engagement, and iterative testing.

These findings informed recommendations for a Circular Design Guide, offering practical steps to embed circularity into everyday medical device development. The research demonstrates that circular design in healthcare is achievable when environmental ambitions are balanced with clinical, regulatory, and operational realities.

Beyond individual devices, the work emphasizes broader implications. Collaboration across disciplines and organizations, digital tools to track and optimize device lifecycles, and education to embed circular thinking into practice are essential to scaling impact. Overall, this dissertation shows that sustainability and circularity in healthcare are not abstract ideals, but actionable approaches supported by tools such as the visual taxonomy and Circular Design Guide for medical devices, which can guide policy, industry practice, and future research. ...
Like many health devices, smart pill boxes designed to enhance medication adherence often incorporate electronic components and smart sensors. However, the production and disposal of these rising numbers of electronics contribute significantly to the global e-waste crisis, exacerbating the negative climate impact of the healthcare industry. To minimize the impact of such electronic health devices, redesign based on circular economy principles is crucial. However, currently no clear circular design methodology exists to apply those principles in the healthcare domain. This paper discusses a case study in which we propose conceptual redesigns that aim to mitigate the environmental impact of smart pill boxes and help align them with circular economy principles. We employ a research-through-design approach in which we attempt to apply the well-known “10R strategies” (i.e. refuse, rethink, reduce, reuse, repair, refurbish, remanufacture, repurpose, recycle, and recover) as a design method. While doing this, we assessed their applicability in a design process and added value in making the device circular through reflective journalling, and their estimated effectiveness on minimizing environmental impacts by comparing fast-track LCAs for each design decision. In this way, we were able to provide insights into the intricacies of designing a more sustainable and circular device in this manner, and subsequently formulate recommendations for designing similar devices in the future. ...

Barriers, opportunities and best practices from a design perspective

In an era of electronics-driven healthcare, the disposability of many medical devices raises environmental concerns. Transitioning these devices towards a circular economy, involving practices like reuse, remanufacturing, and recycling, holds promise. Our paper explores this transition through desk research, literature review, and expert interviews, examining the current state of circular design in electronic medical devices. We unveil barriers, opportunities, and design recommendations for circularization. First, we highlight the circularity potential of medical devices currently on the market, implementing e.g. refuse, reuse, recycle, etc. Second, we present barriers for circular medical device design, (e.g. (perceived) safety and infection risks, (perceived) regulatory difficulties, financial constraints, and difficulties in collection and separation) and opportunities to overcome these barriers. Finally, we present 29 design-specific recommendations for creating circular medical devices. Our insights into circular healthcare practices urge design engineers to integrate sustainable principles into medical device development without compromising safety, quality, or functionality. ...
Journal article (2022) - Harm J. Scholten, Yomi Hoever, Elke Kanters, Tamara Hoveling, Marco de Wild, Erik H.M. Korsten, R. Arthur Bouwman
Journal article (2022) - Harm J. Scholten, Yomi Hoever, Fredericus H. J. van Loon, Elke Kanters, Tamara Hoveling, Marco de Wild, R. Arthur Bouwman, Erik H.M. Korsten
Study objective: The three-dimensional shape of the ultrasound beam produces a thicker scan plane than most users assume. Viewed longitudinally, a needle placed lateral to a vessel just outside the central scanning plane can be displayed incorrectly in the ultrasound image as if placed intravascularly. This phenomenon is called the beam width artefact, also known as the elevation or slice thickness artefact. The goal of this study was to demonstrate the potential negative effect of the beam width artefact on the performance of in-plane ultrasound-guided vascular access procedures, and to provide a solution. Design: Randomized, double-blinded study Setting: Department of anaesthesiology and intensive care of a teaching hospital Participants: 31 experienced (anesthesiologists and intensivists) and 36 inexperienced (anesthetic nurses) ultrasound users Interventions: We developed an acoustic lens that narrows the scan plane to reduce the beam width artefact. The lens was tested in a simulated vascular access study. Measurements: The primary endpoint was first pass success. Secondary endpoints were the number of punctures and needle withdrawals, procedure time, needle visibility and operator satisfaction. Main results: First pass success was highly enhanced using the acoustic lens, with a success rate of 92.5% versus 68.7% without the lens (difference 23.8, 95% confidence interval 11.0–35.3, p < 0.001). The total number of punctures needed to obtain intravenous access was also reduced using the lens (1.10 versus 1.38, difference 0.27, 95% CI 0.11–0.43, p = 0.002). Procedure time, needle withdrawals, needle visibility and satisfaction were similar. Both inexperienced and experienced users benefited from the acoustic lens. Conclusions: The beam width artefact has a significant effect on the performance of ultrasound-guided needle-based procedures. The efficacy of in-plane superficial vascular access procedures can be enhanced by narrowing the imaging plane using an acoustic lens. ...
Conference paper (2021) - Tamara Hoveling, Juliette van Haren, Frank Delbressine
Extremely premature babies (24 to 28 weeks) have underdeveloped bodies, resulting in a survival rate of only 50-70%. To increase this rate, researchers around the globe are developing an artificial womb (AW), a safe environment that mimics the natural uterus, allowing the fetus to develop further. To successfully transfer the fetus from the natural uterus to the AW - while avoiding the respiratory reflex and thus neonatal transition - it is important that no air enters the lungs. To improve safety and minimize animal testing, the transfer procedure is first tested and trained using a fetal manikin simulation. To this end, the intent of this study was to perform a literature analysis to understand how the breathing reflex of a premature infant can be simulated in a fetal manikin. This study resulted in an overview of triggers known to initiate the respiration at birth and ways to detect these triggers, leading to a proposal for an electromechanical system. This proposal was incorporated into a realistic-looking prototype, which was subsequently evaluated with medical end users. ...
Conference paper (2021) - Lu Liu, Tamara Hoveling, Panos Markopoulos
Design fiction (DF) is gaining ground as an approach that helps designers to explore possible futures. As a method founded upon critical attitudes and creative thinking, DF may be challenging for design students. In this study, we explore how design students use DF during creative design activities. Students engaged in an individual digital brainstorm and an in-depth, semi-structured interview about their experiences with the brainstorm based on DF. The results show that DF can be challenging for students who do not have a clear appreciation of what is technologically feasible for a particular time frame in the future and do not yet have the breadth of knowledge to argue about broader topics that DF is particularly attuned to into the discussion as, for example, economics and societal norms. This study contributes insights into how DF impacts the students’ design thinking, as well as difficulties they had regarding their individual thinking process. ...