Objectives Patients resuscitated from an out‐of‐hospital circulatory arrest (OHCA) commonly present without an obvious etiology. We assessed the diagnostic capability and safety of early head‐to‐pelvis computed tomography (CT) imaging in such patients. Methods From November 2015 to February 2018, we enrolled 104 patients resuscitated from OHCA without obvious cause (idiopathic OHCA) to an early sudden‐death CT (SDCT) scan protocol within 6 h of hospital arrival. The SDCT protocol included a noncontrast CT head, an electrocardiogram‐gated cardiac and thoracic CT angiogram, and a nongated venous‐phase abdominopelvic CT angiogram. Patients needing urgent cardiac catheterization or hemodynamically unable to tolerate SDCT were excluded. Cardiac CT analyses were blinded, but other SDCT findings were clinically available. Primary endpoints were the number of OHCA causes identified by SDCT compared to the adjudicated cause and critical diagnoses identified by SDCT, including resuscitation complications. Safety endpoints were acute kidney injury (AKI) and inappropriate treatments based on SDCT findings. Acute coronary syndrome was the presumed etiology if any major coronary artery had a >50% stenosis without another OHCA cause. Results SDCT scans occurred within 1.9 ± 1.0 h of hospital arrival and identified 39% (41/104) of all OHCA causes and 95% (39/41) of causes potentially identifiable by SDCT. Critical findings were identified by SDCT in 98% (43/44) of patients that included potentially life‐threatening resuscitation complications of liver or spleen laceration (n = 6); pneumothorax or thoracic organ laceration (n = 8); and mediastinal, pericardial, or vascular hemorrhage (n = 3). SDCT exclusively identified 13 (13%) OHCA causes that would otherwise not be identified without SDCT imaging. No inappropriate treatments resulted from SDCT findings. AKI was common (28%) but only one (1%) patient required new dialysis. Conclusions This observational cohort study suggests that early SDCT scanning is safe, can expedite the diagnosis of potential causes, and can meaningfully change clinical management after idiopathic OHCA.

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The design of medical technologies for developing countries is a multidisciplinary process. We describe a model process for an appropriate medical device design. D-Lab Health combines real world projects and partners with a diverse student team to provide experiential educational opportunities in a developing country health care setting; in turn, the partners benefit from student medical device designs. In order to effectively communicate practical design strategies toward an appropriate design for medical technology, a series of accelerated technology learning modules was developed using commercially available and customized medical devices. Each module included a formal framework for the students to think about the competing priorities of the user, chooser, payer, and approver of such global health technologies, christened the "global health innovation compass." These modules provided a hands-on laboratory experience that demystified the design process. This was particularly useful for nonengineering students who were able to add value to the project through their life-sciences background. An essential component of the course was a weeklong visit to our field partners in Nicaragua to enable the students to get first hand experience and to identify a health need they could address with a technology solution. Subsequently, the students utilized their hands-on training to develop medical device prototypes within an abbreviated production schedule of 3 weeks. We describe the design process for one such prototype "a low cost glucometer."The current methodologies of clinical heart transplantation limit the ischemic window to 4-6 h. Periods longer than this can induce dysfunction in the organ and can lead to increased patient morbidity and mortality. An alternative to the current methods of static cold storage ͑CS͒ is continuous hypothermic perfusion ͑CHP͒, where a hypothermic oxygenated crystalloid solution is mechanically perfused through the coronary arteries. This has been shown to preserve the function for up to 72 h, but the techniques have yet to be optimized. We have developed an apparatus and methodology for performing CHP on large mammalian hearts, followed by reanimation in our in vitro Langendorff apparatus ͑The Visible Heart TM ͒. We are also investigating the utility of the cardioprotective agents docosahexaenoic acid and ͓D-Ala2, D-Leu5͔ enkephalin, both of which have shown cardioprotective effects in our laboratory, and we believe that their addition to the preservation solution can further extend the transplant window. A series of pilot studies has been performed to date, with modestly successful results. Hearts preserved with CHP seem to show better functionality than CS hearts but far worse functionality than hearts reanimated immediately after explant. We hope to use this system to optimize CHP methodology and eventually develop a system for prolonging the window for heart transplantation.

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