Ulrik Kihlbom

Ulrik Kihlbom

Professor
E-postadress: ulrik.kihlbom@ki.se
Telefon: +46852483653
Mobiltelefon: +46705156040
Besöksadress: Widerströmska huset, Tomtebodavägen 18A, 17165 Solna
Postadress: C7 Lärande, Informatik, Management och Etik, C7 Etik Helgesson, 171 77 Stockholm

Om mig

  • Jag är professor i medicinsk klinisk etik vid Etikenheten och arbetar inom min forskning främst med medicinetiska frågor som rör patienters perspektiv och beslutsfattande inom hälso- och sjukvård. Andra forskningsintressen rör etik inom socialtjänst, folkhälsa och den praktiska etikens metodologi. För närvarande leder jag det tvärvetenskapliga projektet "För barnets bästa? Etiska, juridiska och empiriska undersökningar av socialtjänstbeslut om umgängesbegränsningar", finansierat av Vetenskapsrådet (2024-2026) med forskare från filosofi, folkhälsovetenskap, juridik och socialt arbete (se länk till projektets hemsida till höger på denna sida). Sedan mars 2023 arbetar jag även i ett ERAPerMed-projekt som handlar om att personanpassa interventioner för att mildra tidiga MS-symptom.

    Jag undervisar på flera kurser vid läkarprogrammet och andra utbildningar inom KI såväl som för anställda inom hälso- och sjukvården. Jag är också medlem i Karolinska universitetsjukhusets etikråd, barnetikrådet vid Astrid Lindgrens barnsjukhus och i SBUs vetenskapliga råd, samt i LIME-institutionens utbildningsnämnd. 

Artiklar

Alla övriga publikationer

  • Book chapter: ETHICAL CHALLENGES IN CANCER DIAGNOSIS AND THERAPY: RECENT RESULTS IN CANCER RESEARCH. 2021;p. 119-134
    Ethical Aspects of Regulating Oncology Products
    Kihlbom U; Guizzaro L; Drosos S; Pignatti F
  • Book chapter: ETHICAL, SOCIAL AND PSYCHOLOGICAL IMPACTS OF GENOMIC RISK COMMUNICATION. 2020;p.
    Introduction
    Kihlbom U
  • Book chapter: ETHICAL, SOCIAL AND PSYCHOLOGICAL IMPACTS OF GENOMIC RISK COMMUNICATION. 2020;p.
    "They don't really understand"
    Kihlbom U
  • Book: 2020
    Ethical, Social and Psychological Impacts of Genomic Risk Communication
    Kihlbom U; Hansson MG; Schicktanz S
  • Book chapter: ETHICAL, SOCIAL AND PSYCHOLOGICAL IMPACTS OF GENOMIC RISK COMMUNICATION. 2020;p.
    Epilogue
    Kihlbom U
  • Book chapter: WHAT ABOUT THE FAMILY? PRACTICES OF RESPONSIBILITY IN CARE. 2019;p.
    Healthcare Decisions
    Kihlbom U; Munthe C
  • Review: ADVANCES IN AGGREGATION INDUCED EMISSION MATERIALS IN BIOSENSING AND IMAGING FOR BIOMEDICAL APPLICATIONS, PT A. 2018;158:299-323
    Renzi C; Provencal N; Bassil KC; Evers K; Kihlbom U; Radford EJ; Koupil I; Mueller-Myhsok B; Hansson MG; Rutten BPF
  • Published conference paper: BIOETHICS. 2000;14(4):287-309
    Kihlbom U

Forskningsbidrag

  • Swedish Research Council for Health Working Life and Welfare
    1 January 2025 - 31 December 2027
    Research problem and specific questionsSuicide prevention is a high-priority public health goal. Assessing patients´ suicide risk is a basis for clinical decisions in psychiatry, including decisions about involuntary care. However, there is currently a lack of clear evidence on how suicide risk should be assessed and how risk assessments should be used, leading to uncertainty and possible inequality in clinical assessments and decisions.- How are suicide risk assessments conducted and what basis do they provide for clinical decisions, including decisions about involuntary care?- How do patients perceive suicide risk assessments and what is their view on the role of suicide risk assessments in psychiatry?- How do judges perceive suicide risk assessments and what relevance do they have for court decisions regarding involuntary psychiatric care?- How should suicide risk assessments be conducted and how should they be used in healthcare?Data and methods1) Interviews with psychiatrists about how they conduct suicide risk assessments and how they use their assessments. The data will be analyzed using qualitative content analysis.2) Interviews with patients about their experiences and views of suicide risk assessments. We will use thematic analysis to analyse the data.3) A survey study based on case vignettes and questions on suicide risk assessments and involuntary psychiatric care. The survey will be sent to Swedish psychiatrists. We will use descriptive and inferential methods to analyze the results.4) Focus group interviews with judges in the Administrative Courts regarding suicide risk as a reason for involuntary psychiatric care. We will use qualitative content analysis to analyze the data. 5) Ethical analysis based on studies 1-4 and current research on suicide prediction. The aim is to present an analysis and an ethical framework to guide assessments of suicide risk in healthcare.Social Relevance and utilisationThe overarching goal of the project is to provide a basis for evidence-based, clinically meaningful, equal, and patient-centered assessments of suicide risk.Plan for project realisationThe project will be conducted over three years by an interdisciplinary research team that includes expertise in psychiatry, medical ethics, and law. We intend to publish the results in the form of research articles and also to develop a framework for suicide risk assessments to be used as decision support in healthcare
  • Swedish Research Council
    1 January 2024 - 31 December 2026
    The overall purpose of this project is to critically explore decision making in social care with a focus on the principle of the “best interest of the child” in matters related to restricting children’s and legal guardians’ right to socialization in compulsory care. We will take an interdisciplinary approach in examining the ethical and legal foundations of the principle of the best interest of the child, exploring how it is understood and applied by social workers in this decision-making context. On these grounds and in collaboration with social workers as research partners, we will develop recommendations and tools to support decision-making.The specific aims of this project are to:Identify and assess the legal and ethical principles and values that underpin the notion of the best interest of the child.Identify how social workers in Sweden understand and apply the notion of the best interest of the child in the context of making decisions about restricting children’s contact with their parents.Formulate the most reasonable ethical and legal requirements for making decisions guided by the best interest of the child in social care.Develop the first stages of an intervention that in may inform and support decisions in social care.By using methods of legal science, analytic philosophy, qualitative and quantitative empirical methodology and social interventions, the results will be relevant to scholars in different fields as well as to social workers and other stakeholders.
  • RELIABLE
    ERA PerMed/Vinnova
    1 March 2022 - 28 February 2025
  • Innovative Medicines Initiative (IMI) 2
    1 October 2016 - 31 May 2022

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