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The use of virtual nominal groups in healthcare research: An extended scoping review.

IntroductionThe Nominal Group Technique (NGT) is a consensus group method used to synthesize expert opinions. Given the global shift to virtual meetings, the extent to which researchers leveraged virtual platforms is unclear. This scoping review explores the use of the vNGT in healthcare research during the COVID-19 pandemic.MethodsFollowing the Arksey and O'Malley's framework, eight cross-disciplinary databases were searched (January 2020-July 2022). Research articles that reported all four vNGT stages (idea generation, round robin sharing, clarification, voting) were included. Media Synchron

Psychometric properties of the Chinese version of the M.D. Anderson symptom Inventory-Multiple Myeloma Module: a translation and validation study.

BACKGROUND: The reliability of the M.D. Anderson Symptom Inventory-Multiple Myeloma Module (MDASI-MM) was evaluated through its Chinese translation among Chinese patients with multiple myeloma. METHODS: The MDASI-MM scale underwent translation into Chinese following Brislin's two-way translation paradigm, incorporating ortho-translation, back-translation, pre-surveying, and cultural adaptation. The scale's validity and reliability were assessed using a sample of five hundred multiple myeloma patients from three tertiary general hospitals in Zhejiang Province, China, selected through convenien

Психометрическая оценка шкалы восприятия искусственного интеллекта для больных раком: подход к структурному уравнению.

РАЦИОНАЛЬ, ЦЕЛИ И ЗАДАЧИ: Искусственный интеллект (ИИ) всё более интегрируется в онкологическую помощь, и онкологические сестры играют ключевую роль в образовании пациентов, коммуникации и восприятии этих технологий. Несмотря на то, что ИИ всё более интегрируется в здравоохранение, существующие шкалы восприятия ИИ и принятия технологий в основном были разработаны для общих здравоохранительных условий и не достаточно отражают уникальные клинические, этические и связанные с рабочим процессом аспекты онкологической практики. Целью этой работы было разработка и психометрическая валидация шкалы, из

Health-related quality of life domains relevant to people in Europe undergoing cancer treatment: a systematic review of qualitative research.

PurposeTo identify and synthesize evidence from European qualitative studies on cancer-related quality of life outcomes, needs, experiences, preferences, and concerns of people undergoing cancer treatment in the last decade.MethodsSystematic review ( https://www.crd.york.ac.uk/PROSPERO , CRD42024575065) of European studies using qualitative methodology, assessing constructs related to HRQoL, and involving adults receiving cancer treatment. The search was performed in PubMed and Scopus from January 2013 to July 2024. Titles, abstracts, and full texts screening, data extraction and risk of bias

Онко@home: сопоставление стоимости и возмещения расходов на лечение рака на дому со стандартом медицинского обслуживания.

СПРАВОЧНАЯ ИНФОРМАЦИЯ: Онкологическая госпитализация на дому (HH) была осуществлена в бельгийском контексте для оценки осуществимости онкологической госпитализации на дому. В первой модели HH (HH1), реализованной three Бельгийские больницы, two Организации по уходу на дому и группа независимых медсестер, анализ крови и наблюдение перед внутривенной терапией проводились квалифицированной домашней медсестрой в доме пациента за день до посещения дневной больницы. В рамках второй модели HH (HH2), внедренной в one госпиталь, администрация two Лечение подкожного (Azacitidine and Bortezomib) миэлодип

Воздействие онлайновой программы поддержки пациентов под руководством медсестер на усталость, сон и качество жизни у пациентов с множественным склерозом: квазиэкспериментальное исследование.

Множественный склероз (MS) становится все более распространенным. Физические расстройства и проблемы со сном, особенно усталость, ухудшают качество жизни этих пациентов. One Одним из наиболее успешных и долгосрочных стратегий борьбы с симптомами является обучение пациентов. Цель этого исследования заключалась в оценке воздействия онлайновой программы поддержки под руководством медсестер на усталость, сон и качество жизни пациентов с множественным склерозом (PwMS). МЕТОДЫ: Это квазиэкспериментальное исследование было проведено в амбулаторной клинике MS одной из университетских больниц в Стамбул

European Cancer Organisation Essential Requirements for Quality Cancer Care: Hematological malignancies.

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Staff perspectives on the feasibility of a clinical pathway for anxiety and depression in cancer care, and mid-implementation adaptations.

BackgroundClinical pathways (CPs) are intended to standardise and improve care but do not always produce positive outcomes, possibly because they were not adapted to suit the specific context in which they were enacted. This qualitative study aimed to explore staff perspectives of implementation of a CP for routine screening, assessment, referral and management of anxiety and depression (the ADAPT CP) for patients with cancer, focussing on perceived feasibility of the CP and negotiated adaptations made during the implementation phase.MethodsThe ADAPT CP was implemented in 12 urban and regional

Transforming End-of-Life Care

Currently, hospice care which focuses on caring for a terminally ill person delivers holistic, supportive, interdisciplinary, and patient-centered management. There have been nu-merous efforts to establish hospice care for people who are in the end-stage of their illness.

Navigating isolation- barriers and multidimensional support needs in symptom self-management for HSCT patients within laminar airflow rooms: a descriptive qualitative study.

BACKGROUND: Hematopoietic stem cell transplantation (HSCT) is a crucial therapy for hematological malignancies and other conditions. However, the intensive therapy and required isolation place significant physical and psychological burdens on patients. Although effective symptom self-management during isolation is pivotal, the current efforts are often challenged, leading to distress and feelings of loss of control. Nevertheless, research specifically addressing the self-management needs and barriers faced by patients with HSCT confined to laminar airflow rooms is limited. This study aimed to

The SMARTIE Program: A Novel Initiative to Evaluate the Impact of AP Continuing Education on Clinical Practice.

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Cost analysis of skeletal-related events in Spanish patients with bone metastases from solid tumours.

PurposeTo estimate the cost per skeletal-related event (SRE) in patients with bone metastases secondary to solid tumours in the Spanish healthcare setting.MethodsPatients diagnosed with bone metastases secondary to breast, prostate or lung cancer were included in this multicentre, observational study. SREs are defined as pathologic fracture (vertebral and non-vertebral fracture), radiation to bone, spinal cord compression or surgery to bone. Health resource utilisation associated with these events (inpatient stays, outpatient, emergency room and home health visits, nursing home stays and proce

Strategies to improve patient-reported outcome completion rates in longitudinal studies.

PURPOSE: The quality of patient-reported outcome (PRO) data can be compromised by non-response (NR) to scheduled questionnaires, particularly if reasons for NR are related to health problems, which may lead to unintended bias. The aim was to investigate whether electronic reminders and real-time monitoring improve PRO completion rate. METHODS: The population-based study "Quality of life in Danish multiple myeloma patients" is a longitudinal, multicentre study with consecutive inclusion of treatment-demanding newly diagnosed or relapsed patients with multiple myeloma. Education of study nurses

Using journey mapping to understand the experience and need for patients with chimeric antigen receptor T-cell therapy.

ObjectiveTo map the journey and needs of patients receiving chimeric antigen receptor T-cell (CAR-T) therapy, providing a reference for improving the comprehensive management of patients receiving clinical CAR-T cell therapy, as well as enhancing patients' overall well-being.MethodsA qualitative grounded theory approach was used. From August 2024 to January 2025, patients receiving CAR-T cell therapy at a university hospital in Wuhan, China, were enrolled through purposive sampling. The research data were collected from descriptive observation, focused observation, and selective observation. T

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… Advanced practice nursing and CAR-t cell therapy: opportunities, challenges and future directions Semin Oncol Nurs 40 2024 151628 10.1016/j.soncn.2024.151628 38594105 3 Hayden P.J. Roddie C. Bader P. …

Tablet Acceptability in Older Outpatients Undergoing Cancer Chemotherapy.

Background/Objectives: Patient acceptability of oral anticancer drugs is a critical factor that influences treatment in older outpatients receiving cancer chemotherapy and plays a central role in enhancing adherence and treatment effectiveness. Identifying older outpatients receiving cancer chemotherapy who exhibit poor tablet acceptability before initiating oral anticancer therapy and offering alternative treatment options are beneficial. Therefore, we investigated the characteristics of patients with poor tablet acceptability by focusing on the tablet size, geriatric assessment, and polyphar

The use of smart technologies for enhancing palliative care: A systematic review.

IntroductionWith the rapid advancement of technology, smart technologies have permeated various sectors, including palliative care in healthcare. Based on the available literature, similar studies have elucidated the application of individual and isolated smart technologies in palliative care, with their benefits, and limitations. This research, therefore, focuses on the conceptualisation of various smart technologies and makes holistic recommendations on the effective and efficient use of smart technologies in healthcare to enhance palliative care.PurposeThe purpose of this study is to system

How to talk about death? A cross-sectional survey on patients', informal caregivers' and health care professionals' views in the setting of allogenic hematopoietic stem cell transplantation.

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a potentially curative treatment, which carries a high risk of complications and mortality, highlighting the necessity of discussions about life threat. This study explores the perspectives of patients, informal caregivers (ICs), and healthcare professionals (HCPs) regarding the timing, content, and challenges of these discussions. Multicenter cross-sectional survey in comprehensive care centers across Germany, involving patients with allo-HSCT, ICs, and HCPs. Questionnaires assessed perceived concerns about life threat, communi

The first hematopoietic stem cell transplantation centre in Iraqi Kurdistan: nursing perspectives and education.

AimTo describe the nursing capacity-building process within the foundation of a hematopoietic stem cell transplantation (HSCT) centre at the Hiwa Cancer Hospital (HCH), Sulaymaniyah, Iraqi Kurdistan, referring to nursing education, empowerment and leadership.Methods1) Capacity building, the process by which individuals, organisations, institutions and societies develop abilities to perform functions, solve problems and set and achieve objectives, was implemented; 2) Nurse intervention was based exclusively on training and coaching on site, which is an innovative approach, since more often expe

Качество жизни людей с множественным склерозом в Португалии.

ВВЕДЕНИЕ: Множественный склероз существенно влияет на качество жизни тех, кто страдает от этого конкретного состояния. ЦЕЛЬ: Оценка качества жизни людей с множественным склерозом и анализ взаимосвязи между болезнью и связанными с ней последствиями и различными социально-демографическими, клиническими и функциональными переменными. МАТЕРИАЛЫ И МЕТОДЫ: Наблюдение, перекрестное, описательное и количественное исследование, проведенное с использованием непробивной удобной выборки, состоящей из 70 пациентов, страдающих множественным склерозом, зарегистрированных Ассоциацией по множественному склероз

Managing Matajoosh: determinants of first Nations' cancer care decisions.

BackgroundAccessing cancer treatment requires First Nation peoples living in rural and remote communities to either commute to care, or to relocate to an urban centre for the length or part of the treatment. While Canadians living in rural and remote communities must often make difficult decisions following a cancer diagnosis, such decisions are further complicated by the unique policy and socio-historical contexts affecting many First Nation peoples in Canada. These contexts often intersect with negative healthcare experiences which can be related to jurisdictional confusion encountered when