Reliable vital sign assessments are crucial for the management of patients with infectious diseases. Wearable devices enable easy and comfortable continuous monitoring across settings, especially in pediatric patients, but information about their performance in acutely unwell children is scarce. Vital signs were continuously measured with a multi-sensor wearable device (Everion^®, Biofourmis, Zurich, Switzerland) in 21 pediatric patients during their hospitalization for appendicitis, osteomyelitis, or septic arthritis to describe acceptance and feasibility and to compare validity and reliability with conventional measurements. Using a wearable device was highly accepted and feasible for health-care workers, parents, and children. There were substantial data gaps in continuous monitoring up to 24 h. The wearable device measured heart rate and oxygen saturation reliably (mean difference, 2.5 bpm and 0.4% SpO₂) but underestimated body temperature by 1.7 °C. Data availability was suboptimal during the study period, but a good relationship was determined between wearable device and conventional measurements for heart rate and oxygen saturation. Acceptance and feasibility were high in all study groups. We recommend that wearable devices designed for medical use in children be validated in the targeted population to assure future high-quality continuous vital sign assessments in an easy and non-burdening way.

Background/Objectives: Atrial fibrillation (AF) remains a major risk factor for stroke. It is often asymptomatic and paroxysmal, making it difficult to detect with conventional electrocardiography (ECG). While photoplethysmography (PPG)-based devices like smartwatches have demonstrated efficacy in detecting AF, they are rarely integrated into hospital infrastructure. The study aimed to establish a seamless system for real-time AF screening in hospitalized high-risk patients using a wrist-worn PPG device integrated into a hospital’s data infrastructure. Methods: In this investigator-initiated prospective clinical trial conducted at the University Hospital Basel, patients with a CHA₂DS₂-VASc score ≥ 2 and no history of AF received a wristband equipped with a PPG sensor for continuous monitoring during their hospital stay. The PPG data were automatically transmitted, analyzed, stored, and visualized. Upon detection of an absolute arrhythmia (AA) in the PPG signal, a Holter ECG was administered. Results: The analysis encompassed 346 patients (mean age 72 ± 10 years, 175 females (50.6%), mean CHA₂DS₂-VASc score 3.5 ± 1.3)). The mean monitoring duration was 4.3 ± 4.4 days. AA in the PPG signal was detected in twelve patients (3.5%, CI: 1.5–5.4%), with most cases identified within 24 h (p = 0.004). There was a 1.3 times higher AA burden during the nighttime compared to daytime (p = 0.03). Compliance was high (304/346, 87.9%). No instances of AF were confirmed in the nine patients undergoing Holter ECG. Conclusions: This study successfully pioneered an automated infrastructure for AF screening in hospitalized patients through the use of wrist-worn PPG devices. This implementation allowed for real-time data visualization and intervention in the form of a Holter ECG. The high compliance and early AA detection achieved in this study underscore the potential and relevance of this novel infrastructure in clinical practice.

Background: The transition from hospital to primary care is a vulnerable period for patients. Telemedicine may enhance continuity of care; however, evidence on its role in supporting hospital-to-primary-care transitions remains limited. Objective: We implemented and evaluated a telephone-based follow-up program to support the transition from hospital to home and primary care, focusing on patient health as well as patient and health care provider satisfaction. Methods: In this prospective, single-center intervention study (University Hospital Basel, September 2022-December 2024), 234 patients discharged from the emergency unit or internal medicine wards received structured telemedical follow-up for up to 10 days until their first primary care appointment. Primary outcomes were patient health and satisfaction; secondary outcomes were health care provider satisfaction. Data were collected using patient-reported outcome measures, patient-reported experience measures, and provider assessments and analyzed descriptively and analytically ( P =.05). Results: Patient-reported outcome measure and patient-reported experience measure scores changed during follow-up, while no deterioration was observed. Health care provider satisfaction varied, with telemedical physicians reporting the highest ratings, hospital physicians intermediate ratings, and general practitioners the lowest, citing challenges in information transfer and perceived added value. Conclusions: This study outlines both the potential benefits and the practical challenges of implementing a telephone follow-up program after hospital discharge. Variations in physician satisfaction highlight the need for more user-friendly technical infrastructure and clearer role definitions. Future multicenter studies with broader patient samples, usual care controls, and simplified recruitment processes are required to strengthen the feasibility and generalizability of this approach.