Background: Improving physical activity, especially in combination with optimizing protein intake, after surgery has a potential positive effect on recovery of physical functioning in patients after gastrointestinal and lung cancer surgery. The aim of this randomized controlled trial is to evaluate the efficacy of a blended intervention to improve physical activity and protein intake after hospital discharge on recovery of physical functioning in these patients. Methods: In this multicenter single-blinded randomized controlled trial, 161 adult patients scheduled for elective gastrointestinal or lung cancer surgery will be randomly assigned to the intervention or control group. The purpose of the Optimal Physical Recovery After Hospitalization (OPRAH) intervention is to encourage self-management of patients in their functional recovery, by using a smartphone application and corresponding accelerometer in combination with coaching by a physiotherapist and dietician during three months after hospital discharge. Study outcomes will be measured prior to surgery (baseline) and one, four, eight, and twelve weeks and six months after hospital discharge. The primary outcome is recovery in physical functioning six months after surgery, and the most important secondary outcome is physical activity. Other outcomes include lean body mass, muscle mass, protein intake, symptoms, physical performance, self-reported limitations in activities and participation, self-efficacy, hospital readmissions and adverse events. Discussion: The results of this study will demonstrate whether a blended intervention to support patients increasing their level of physical activity and protein intake after hospital discharge improves recovery in physical functioning in patients after gastrointestinal and lung cancer surgery. Trial registration: The trial has been registered at the International Clinical Trials Registry Platform at 14–10-2021 with registration number NL9793. Trial registration data are presented in Table 1.
Background: Optimizing transitional care by practicing family-centered care might reduce unplanned events for patients who undergo major abdominal cancer surgery. However, it remains unknown whether involving family caregivers in patients’ healthcare also has negative consequences for patient safety. This study assessed the safety of family involvement in patients’ healthcare by examining the cause of unplanned events in patients who participated in a family involvement program (FIP) after major abdominal cancer surgery. Methods: This is a secondary analysis focusing on the intervention group of a prospective cohort study conducted in the Netherlands. Data were collected from April 2019 to May 2022. Participants in the intervention group were patients who engaged in a FIP. Unplanned events were analyzed, and root causes were identified using the medical version of a prevention- and recovery-information system for monitoring and analysis (PRISMA) that analyses unintended events in healthcare. Unplanned events were compared between patients who received care from family caregivers and patients who received professional at-home care after discharge. A Mann-Whitney U test was used to analyze data. Results: Of the 152 FIP participants, 68 experienced an unplanned event and were included. 112 unplanned events occurred with 145 root causes since some unplanned events had several root causes. Most root causes of unplanned events were patient-related factors (n = 109, 75%), such as patient characteristics and disease-related factors. No root causes due to inadequate healthcare from the family caregiver were identified. Unplanned events did not differ statistically (interquartile range 1–2) (p = 0.35) between patients who received care from trained family caregivers and those who received professional at-home care after discharge. Conclusion: Based on the insights from the root-cause analysis in this prospective multicenter study, it appears that unplanned emergency room visits and hospital readmissions are not related to the active involvement of family caregivers in surgical follow-up care. Moreover, surgical follow-up care by trained family caregivers during hospitalization was not associated with increased rates of unplanned adverse events. Hence, the concept of active family involvement by proficiently trained family caregivers in postoperative care appears safe and feasible for patients undergoing major abdominal surgery.
Background: Major surgery is associated with negative postoperative outcomes such as complications and delayed or poor recovery. Multimodal prehabilitation can help to reduce the negative effects of major surgery. Offering prehabilitation by means of mobile health (mHealth) could be an effective new approach. Objective: The objectives of this pilot study were to (1) evaluate the usability of the Be Prepared mHealth app prototype for people undergoing major surgery, (2) explore whether the app was capable of bringing about a change in risk behaviors, and (3) estimate a preliminary effect of the app on functional recovery after major surgery. Methods: A mixed-methods pilot randomized controlled trial was conducted in two Dutch academic hospitals. In total, 86 people undergoing major surgery participated. Participants in the intervention group received access to the Be Prepared app, a smartphone app using behavior change techniques to address risk behavior prior to surgery. Both groups received care as usual. Usability (System Usability Scale), change in risk behaviors 3 days prior to surgery, and functional recovery 30 days after discharge from hospital (Patient-Reported Outcomes Measurement Information System physical functioning 8-item short form) were assessed using online questionnaires. Quantitative data were analyzed using descriptive statistics, chi-square tests, and multivariable linear regression. Semistructured interviews about the usability of the app were conducted with 12 participants in the intervention group. Thematic analysis was used to analyze qualitative data. Results: Seventy-nine people-40 in the intervention group and 39 in the control group-were available for further analysis. Participants had a median age of 61 (interquartile range 51.0-68.0) years. The System Usability Scale showed that patients considered the Be Prepared app to have acceptable usability (mean 68.2 [SD 18.4]). Interviews supported the usability of the app. The major point of improvement identified was further personalization of the app. Compared with the control group, the intervention group showed an increase in self-reported physical activity and muscle strengthening activities prior to surgery. Also, 2 of 2 frequent alcohol users in the intervention group versus 1 of 9 in the control group drank less alcohol in the run-up to surgery. No difference was found in change of smoking cessation. Between-group analysis showed no meaningful differences in functional recovery after correction for baseline values (β=-2.4 [95% CI -5.9 to 1.1]). Conclusions: The Be Prepared app prototype shows potential in terms of usability and changing risk behavior prior to major surgery. No preliminary effect of the app on functional recovery was found. Points of improvement have been identified with which the app and future research can be optimized. Trial Registration: Netherlands Trial Registry NL8623; https://www.trialregister.nl/trial/8623.
Recycling of plastics plays an important role to reach a climate neutral industry. To come to a sustainable circular use of materials, it is important that recycled plastics can be used for comparable (or ugraded) applications as their original use. QuinLyte innovated a material that can reach this goal. SmartAgain® is a material that is obtained by recycling of high-barrier multilayer films and which maintains its properties after mechanical recycling. It opens the door for many applications, of which the production of a scoliosis brace is a typical example from the medical field. Scoliosis is a sideways curvature of the spine and wearing an orthopedic brace is the common non-invasive treatment to reduce the likelihood of spinal fusion surgery later. The traditional way to make such brace is inaccurate, messy, time- and money-consuming. Because of its nearly unlimited design freedom, 3D FDM-printing is regarded as the ultimate sustainable technique for producing such brace. From a materials point of view, SmartAgain® has the good fit with the mechanical property requirements of scoliosis braces. However, its fast crystallization rate often plays against the FDM-printing process, for example can cause poor layer-layer adhesion. Only when this problem is solved, a reliable brace which is strong, tough, and light weight could be printed via FDM-printing. Zuyd University of Applied Science has, in close collaboration with Maastricht University, built thorough knowledge on tuning crystallization kinetics with the temperature development during printing, resulting in printed products with improved layer-layer adhesion. Because of this knowledge and experience on developing materials for 3D printing, QuinLyte contacted Zuyd to develop a strategy for printing a wearable scoliosis brace of SmartAgain®. In the future a range of other tailor-made products can be envisioned. Thus, the project is in line with the GoChem-themes: raw materials from recycling, 3D printing and upcycling.
De zorg voor mensen met kanker heeft een kantelpunt bereikt. Om de zorg kwalitatief goed, behapbaar, betaalbaar te houden, wordt in toenemende mate ingezet op Passende Zorg, zoals recent beschreven in het Kader Passende Zorg van Zorginstituut Nederland. Dit geldt ook voor groeiende en vergrijzende groep mensen met kanker aan de spijsverteringsorganen (GI-kanker). Zij gaan na een operatie sneller naar huis om te herstellen dan voorheen; hierdoor neemt het belang voor goede herstelzorg toe. Met een sterk consortium van drie ziekenhuizen, een patiëntenorganisatie, twee oncologische samenwerkingsverbanden, drie beroepsverenigingen van paramedici en twee hogescholen, willen wij in het onderzoeksproject PREFERENCE onderzoeken hoe we deze mensen optimaal kunnen ondersteunen in hun fysiek herstel, kwaliteit van leven en participatie. We steken daarbij in op de elementen van Passende Zorg. Op dit moment ontbreekt bij fysiotherapeuten, oefentherapeuten en diëtisten, kennis over hoe ondersteuning in de eerstelijn, dichtbij de patiënt, het best met de patiënt en zorgprofessionals onderling kan plaatsvinden. Stimuleren van eigen regie van de patiënt is daarbij belangrijk. Toch merken zowel zorgverleners als patiënten met GI-kanker dat op dit moment de herstelzorg onvoldoende aansluit bij de behoeften van de patiënt. Ook dierbaren worden op dit moment onvoldoende betrokken. De vragen uit de praktijk leiden tot de onderzoeksvraag: Hoe ziet de optimale, gepersonaliseerde zorg in de eerstelijn eruit voor patiënten na een operatieve verwijdering van GI-kanker ter bevordering van fysiek herstel, participatie en kwaliteit van leven? In vier deelstudies verzamelen we kennis over bestaande behoeften bij patiënten en zorgverleners, identificeren we bestaande oplossingen die aansluiten bij deze behoeften en ontwikkelen, testen en evalueren we een set aan nieuwe oplossingen waarmee de onderlinge samenwerking van alle betrokkenen wordt gestimuleerd en passende (herstel)zorg voor patiënten met GI-kanker en hun dierbaren optimaal wordt ingericht.
In Nederland bezoeken ongeveer 30 op de 1.000 inwoners hun huisarts vanwege schouderklachten, waarvan velen een operatie ondergaan. Na deze operaties dragen patiënten gedurende zes weken een sling, wat vaak leidt tot nachtelijk ongemak en pijn. Het “Schouder- en Elleboog Expertisecentrum" in het Deventer Ziekenhuis voert regelmatig panelgesprekken om de nazorg voor schouderoperaties te evalueren. Uit deze gesprekken blijkt dat patiënten consistent slaapproblemen ervaren na de operatie, vanwege het ontbreken van de middelen voor een comfortabele slaappositie, wat als een belangrijke stressfactor wordt benadrukt. Dit KIEM-project streeft ernaar dit probleem aan te pakken door een innovatief, ergonomisch gevormd kussen te ontwikkelen met een geïntegreerde textiele druksensor in nauwe samenwerking met zowel medische professionals als slaapdeskundigen. De druksensorinformatie wordt gebruikt om inzicht te geven in beweging en drukverdeling om zo het ontwerp van het kussen aan te passen naar een gewenste ondersteuning. Bovendien kunnen kussens met behulp van de juiste drukverdeling worden ontworpen voor verschillende slaaphoudingen en lichaamsbouwen. De samenwerking tussen het Deventer Ziekenhuis, Ducky Dons, Auping, Universiteit Twente en het lectoraat S&FT biedt nieuwe mogelijkheden op het gebied van ergonomische kussens voor medische toepassingen. Dit project resulteert in innovatieve slimme textielmaterialen door geavanceerde technologieën te gebruiken in de Saxion laboratoria, samen met de hoogwaardige textielmaterialen van Ducky Dons. Bovendien zal de Universiteit van Twente de data-analyse uitvoeren, wat essentieel is voor het begrijpen van de resultaten en het optimaliseren van slaap comfort. De functionaliteit van de kussens zal ook worden geanalyseerd en getest met behulp van de testfaciliteiten van Auping, waarbij de betrokkenheid van diverse zorgprofessionals van het Deventer Ziekenhuis van belang is. Het beoogde resultaat is het verbeteren van de slaapkwaliteit en de nazorg voor deze patiëntengroep, evenals het potentieel om een bredere doelgroep te helpen met deze op maat gemaakte oplossing.