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Bahtsevani, Christel
Publikationer (10 of 27) Visa alla publikationer
Axelsson, M., Bahtsevani, C., Neziraj, M., Persson, K. & Kumlien, C. (2023). A registry study of oral health problems and preventive interventions among older persons receiving municipal healthcare - PROSENIOR. Nursing Open, 10(2), 525-534
Öppna denna publikation i ny flik eller fönster >>A registry study of oral health problems and preventive interventions among older persons receiving municipal healthcare - PROSENIOR
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2023 (Engelska)Ingår i: Nursing Open, E-ISSN 2054-1058, Vol. 10, nr 2, s. 525-534Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Aim: The aim was to identify planned and completed preventive interventions among older persons with oral health problems receiving municipal health care. A further aim was to determine the correspondence between oral health problems and planned preventive interventions among older persons with oral health problems receiving municipal health care. Design: Cross-sectional register study. Methods: Oral health data from the Swedish national quality registry, Senior Alert, were extracted for 4,024 older persons (>= 65 years) receiving municipal health care in a county in Southern Sweden. Data were statistically analysed. Results: A large majority of older persons (97.4%) with assessed oral health problems had at least one planned preventive intervention, and approximately three quarters of the planned interventions were completed. There seemed to be a mismatch between type of oral health problems and preventive interventions as not all older persons had a planned preventive intervention related to their specific oral health problem.

Ort, förlag, år, upplaga, sidor
John Wiley & Sons, 2023
Nyckelord
nursing, oral health, prevention, risk assessment, Senior Alert
Nationell ämneskategori
Omvårdnad
Identifikatorer
urn:nbn:se:mau:diva-55110 (URN)10.1002/nop2.1318 (DOI)000851512000001 ()36631732 (PubMedID)2-s2.0-85135862891 (Scopus ID)
Tillgänglig från: 2022-09-23 Skapad: 2022-09-23 Senast uppdaterad: 2024-02-05Bibliografiskt granskad
Appelgren, M., Persson, K., Bahtsevani, C. & Borglin, G. (2022). Swedish registered nurses' perceptions of caring for patients with intellectual and developmental disability: A qualitative descriptive study. Health & Social Care in the Community, 30(3), 1064-1076
Öppna denna publikation i ny flik eller fönster >>Swedish registered nurses' perceptions of caring for patients with intellectual and developmental disability: A qualitative descriptive study
2022 (Engelska)Ingår i: Health & Social Care in the Community, ISSN 0966-0410, E-ISSN 1365-2524, Vol. 30, nr 3, s. 1064-1076Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Patients with intellectual and developmental disability (IDD) are often misinterpreted and misunderstood. Studies show that, in general, healthcare professionals have limited knowledge about IDD, and registered nurses (RNs) often report feeling unprepared to support this group of patients. Therefore, more knowledge about how to adequately address care for this patient group is warranted. This qualitative study employs an interpretative descriptive design to explore and describe Swedish RNs' perceptions of caring for patients with IDD, here in a home-care setting. Twenty RNs were interviewed between September 2018 and May 2019, and the resulting data were analysed through an inductive qualitative content analysis. The study adheres to consolidated criteria for reporting qualitative research (COREQ). Our analysis found that nurses' perceptions of caring for patients with an IDD could be understood from three overarching categories: nursing held hostage in the context of care, care dependent on intuition and proven experience and contending for the patients' right to adequate care. Our findings show that the home-care context and organisation were not adjusted to the needs of the patients. This resulted in RNs feeling unable to provide care in accordance with their professional values. They also explained that they had not mastered the available augmentative and alternative communication tools, instead using support staff as interpreters for their patients. Finally, on a daily basis, the RNs caring for this group of patients took an active stance and fought for the patients' right to receive the right care at the right time by the right person. This was particularly the case with issues involving psychiatric care.

Ort, förlag, år, upplaga, sidor
John Wiley & Sons, 2022
Nyckelord
content analysis, intellectual and development disability, interview, nurses, qualitative research
Nationell ämneskategori
Omvårdnad
Identifikatorer
urn:nbn:se:mau:diva-42492 (URN)10.1111/hsc.13307 (DOI)000651886700001 ()34009687 (PubMedID)2-s2.0-85106260426 (Scopus ID)
Tillgänglig från: 2021-05-31 Skapad: 2021-05-31 Senast uppdaterad: 2024-02-05Bibliografiskt granskad
Wessman, Y. & Bahtsevani, C. (2020). Living with challenges in the shadow of diabetes’: An interview study among adults with diabetic peripheral neuropathy (ed.). Nordic journal of nursing research, 40(2), 73-80
Öppna denna publikation i ny flik eller fönster >>Living with challenges in the shadow of diabetes’: An interview study among adults with diabetic peripheral neuropathy
2020 (Engelska)Ingår i: Nordic journal of nursing research, ISSN 2057-1585, E-ISSN 2057-1593, Vol. 40, nr 2, s. 73-80Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Diabetic peripheral neuropathy is a diabetes-related complication with vague and progressive symptoms with few available treatments. The aim of this study was to describe the experiences of diabetic peripheral neuropathy among adults living with type 1 diabetes. Twelve interviews were performed and qualitative content analysis was used. The overarching theme ‘living with challenges in the shadow of diabetes’ substantiated by the categories ‘pay attention to changes over time’, ‘frequent needs to facilitate living’ and ‘burdens to manage’ represents a daily awareness of the complication where autodidactic strategies were implemented. The conclusion indicates that it might be beneficial if nurses in diabetes care initiate an open-minded dialogue with adults with diabetic peripheral neuropathy to highlight their experiences and to discuss further strategies to facilitate living.

Ort, förlag, år, upplaga, sidor
Sage Publications, 2020
Nyckelord
diabetic peripheral neuropathy, type 1 diabetes, experiences, adults, interview study, qualitative research
Nationell ämneskategori
Medicin och hälsovetenskap
Identifikatorer
urn:nbn:se:mau:diva-4994 (URN)10.1177/2057158519881751 (DOI)2-s2.0-85132251758 (Scopus ID)30793 (Lokalt ID)30793 (Arkivnummer)30793 (OAI)
Tillgänglig från: 2020-02-28 Skapad: 2020-02-28 Senast uppdaterad: 2024-02-05Bibliografiskt granskad
Appelgren, M., Bahtsevani, C., Persson, K. & Borglin, G. (2018). Nurses’ experiences of caring for patients with intellectual developmental disorders: a systematic review using a meta-ethnographic approach (ed.). BMC Nursing, 17, Article ID 51.
Öppna denna publikation i ny flik eller fönster >>Nurses’ experiences of caring for patients with intellectual developmental disorders: a systematic review using a meta-ethnographic approach
2018 (Engelska)Ingår i: BMC Nursing, ISSN 1472-6955, E-ISSN 1472-6955, Vol. 17, artikel-id 51Artikel, forskningsöversikt (Refereegranskat) Published
Abstract [en]

Background: Research suggests that registered nurses (RNs) do not feel adequately prepared to support patients with intellectual disability disorder (IDD). This is unsurprising, as few European health sciences curricula include undergraduate and graduate training courses in IDD. As RNs are often in the front line of care, eliciting in-depth knowledge about how they experience nursing this group of patients is vital. Our aim in this study was to develop a conceptual understanding about RNs’ experiences of nursing patients with IDD. Method: We undertook a systematic review and meta-ethnography to synthesise qualitative research studies found in PubMed, CINAHL, PsycINFO, ERIC databases and by manual searching to identify additional studies. We condensed translatable second-order constructs, and developed an idiomatic translation. Finally, we formulated line of argument (LOA) syntheses to capture the core of the idiomatic translations. Results: We included eighteen published studies from eight countries involving 190 RNs. The RNs’ experience of nursing patients with IDD were reflected in 14 LOAs. Six of these reflected a tentatively more distinctive and at times unique conceptualisation of RNs’ experience of nursing this group of patients. The remaining eight LOAs represented a conceptualisation of nursing per se, a conceptualisation of nursing that was interpreted as a universal experience regardless of context and patient group. Conclusion: Lack of awareness and knowledge are likely breeding grounds for the ‘otherness’ that still surrounds this group of patients. In encounters between patients and RNs, focusing on the person behind the disability label could be one way to secure relevant nursing care for patients with IDD. Undertaking appropriate under- and postgraduate education alongside the implementation of nursing models focusing on patient-centred care would help RNs in reducing the health and care inequalities this group of patients still face.

Ort, förlag, år, upplaga, sidor
Springer Nature, 2018
Nyckelord
Care, Idiomatic Translations, Intellectual developmental disorders, Line of Argument Synthesis, Qualitative Research, Qualitative Synthesis
Nationell ämneskategori
Medicin och hälsovetenskap
Identifikatorer
urn:nbn:se:mau:diva-863 (URN)10.1186/s12912-018-0316-9 (DOI)000451843600001 ()30524202 (PubMedID)2-s2.0-85058953680 (Scopus ID)26919 (Lokalt ID)26919 (Arkivnummer)26919 (OAI)
Tillgänglig från: 2020-02-27 Skapad: 2020-02-27 Senast uppdaterad: 2024-02-06Bibliografiskt granskad
Örmon, K., Sunnqvist, C., Bahtsevani, C. & Torstensson Levander, M. (2016). Disclosure of abuse among female patients within general psychiatric care: a cross sectional study (ed.). BMC Psychiatry (16), Article ID 79.
Öppna denna publikation i ny flik eller fönster >>Disclosure of abuse among female patients within general psychiatric care: a cross sectional study
2016 (Engelska)Ingår i: BMC Psychiatry, E-ISSN 1471-244X, nr 16, artikel-id 79Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Background Experiences of abuse are common among women in general psychiatric care. Even so, there are to our knowledge no previous national or international studies exploring disclosure in a general psychiatric setting of female patient’s experiences of abuse to staff or to formal and informal networks. This study aimed to explore women’s disclosure of experiencing physical, emotional and/or sexual abuse during their most recent contact with staff at a general psychiatric clinic. The study also aimed to determine whether the women have previously disclosed abuse to anyone. Methods A consecutive sampling of eligible female patients at a general psychiatric clinic in an urban area of southern Sweden answered the NorVold Abuse Questionnaire, NorAQ, a self-administrated questionnaire. NorAQ has previously been used and further developed to compare the prevalence of abuse in women present in gynecological outpatient settings in the five Nordic countries. Seventy-seven women with experiences of abuse participated in the research. Descriptive statistics were used to analyse the data. Results Most respondents did not disclose their experiences of abuse to staff at the general psychiatric clinic. Women with experiences of physical abuse (n = 40), emotional abuse (n = 37) and sexual abuse (n = 37) chose not to disclose their experiences. Respondents disclosed abuse more often to others than to staff. Conclusions Our findings indicated the importance of including routine questions concerning abuse experiences as a natural part of female patients’ medical history.

Ort, förlag, år, upplaga, sidor
BioMed Central, 2016
Nyckelord
Adult survivors of abuse, Domestic Violence, Intimate partner violence
Nationell ämneskategori
Medicin och hälsovetenskap
Identifikatorer
urn:nbn:se:mau:diva-14811 (URN)10.1186/s12888-016-0789-6 (DOI)000372740200001 ()27009054 (PubMedID)2-s2.0-84962019974 (Scopus ID)20580 (Lokalt ID)20580 (Arkivnummer)20580 (OAI)
Tillgänglig från: 2020-03-30 Skapad: 2020-03-30 Senast uppdaterad: 2024-02-05Bibliografiskt granskad
Willman, A., Bahtsevani, C., Nilsson, R. & Sandström, B. (2016). Evidensbaserad omvårdnad: en bro mellan forskning och klinisk verksamhe (4., [rev.] uppl.ed.). Studentlitteratur AB
Öppna denna publikation i ny flik eller fönster >>Evidensbaserad omvårdnad: en bro mellan forskning och klinisk verksamhe
2016 (Svenska)Bok (Övrigt vetenskapligt)
Abstract [sv]

Evidensbaserad omvårdnad definieras i denna bok som både ett förhållningssätt och en process. Förhållningssättet innebär en vilja att använda bästa tillgängliga vetenskapliga bevis som underlag för vårdbeslut. Processen består i hur man praktiskt går tillväga för att finna, sammanställa, kritiskt värdera och implementera detta underlag. Evidensbaserad omvårdnad handlar således om en strävan att bedriva omvårdnad på en god och säker grund och att tillgodose samhällets krav på att forskningsresultat utnyttjas på bästa sätt. Denna fjärde upplaga har förtydligats och alla länkar samt webbadresser har uppdaterats. Ett nytt avsnitt om ledarskapets betydelse för implementering av evidens har tillkommit. På bokens webbsida finns en film som visar evidensbaserad omvårdnad i klinisk verksamhet.

Ort, förlag, år, upplaga, sidor
Studentlitteratur AB, 2016. s. 186 Upplaga: 4., [rev.] uppl.
Nyckelord
evidensbaserad omvårdnad, klinisk verksamhet, systematisk litteraturstudie
Nationell ämneskategori
Medicin och hälsovetenskap
Identifikatorer
urn:nbn:se:mau:diva-16133 (URN)20586 (Lokalt ID)978-91-44-10902-2 (ISBN)20586 (Arkivnummer)20586 (OAI)
Tillgänglig från: 2020-03-30 Skapad: 2020-03-30 Senast uppdaterad: 2022-06-27Bibliografiskt granskad
Bahtsevani, C. & Idvall, E. (2016). To Assess Prerequisites Before an Implementation Strategy in an Orthopaedic Department in Sweden (ed.). Orthopedic Nursing, 35(2), 100-107
Öppna denna publikation i ny flik eller fönster >>To Assess Prerequisites Before an Implementation Strategy in an Orthopaedic Department in Sweden
2016 (Engelska)Ingår i: Orthopedic Nursing, ISSN 0744-6020, E-ISSN 1542-538X, Vol. 35, nr 2, s. 100-107Artikel i tidskrift (Refereegranskat)
Abstract [en]

Promoting Action on Research Implementation in Health Services (PARiHS) asserts that the success of knowledge implementation relates to multiple factors in a complex and dynamic way, and therefore the effects of implementation strategies vary by method and context. An instrument based on the PARiHS framework was developed to help assess critical factors influencing implementation strategies so that strategies can be tailored to promote implementation. The purpose of this study was to use the Evaluation Before Implementation Questionnaire (EBIQ), to describe staff perceptions in one orthopaedic department, and to investigate differences between wards. Staff members in four different wards at one orthopaedic department at a university hospital in Sweden were invited to complete a questionnaire related to planning for the implementation of a clinical practice guideline. The 23 items in the EBIQ were expected to capture staff perceptions about the evidence, context, and facilitation factors that influence the implementation process. Descriptive statistics and differences between wards were analyzed. Although the overall response rate was low (n = 49), two of the four wards accounted for most of the completed questionnaires (n = 25 and n = 12, respectively), enabling a comparison of these wards. We found significant differences between respondents' perceptions at the two wards in six items regarding context and facilitation in terms of receptiveness to change, forms of leadership, and evaluation and presence of feedback and facilitators. The EBIQ instrument requires further testing, but there appears to be initial support for pre-implementation use of the EBIQ as a means to enhance planning for implementation.

Ort, förlag, år, upplaga, sidor
Ingenta, 2016
Nyckelord
Nursing, Orthopedics
Nationell ämneskategori
Medicin och hälsovetenskap
Identifikatorer
urn:nbn:se:mau:diva-4654 (URN)10.1097/NOR.0000000000000225 (DOI)000373535200006 ()27028686 (PubMedID)2-s2.0-84962736597 (Scopus ID)21456 (Lokalt ID)21456 (Arkivnummer)21456 (OAI)
Tillgänglig från: 2020-02-28 Skapad: 2020-02-28 Senast uppdaterad: 2024-02-05Bibliografiskt granskad
Janzon, E., Abidi, T. & Bahtsevani, C. (2015). Can physical activity be used as a tool to reduce depression in patients after a cardiac event? What is the evidence? A systematic literature study (ed.). Scandinavian Journal of Psychology, 56(2), 175-181
Öppna denna publikation i ny flik eller fönster >>Can physical activity be used as a tool to reduce depression in patients after a cardiac event? What is the evidence? A systematic literature study
2015 (Engelska)Ingår i: Scandinavian Journal of Psychology, ISSN 0036-5564, E-ISSN 1467-9450, Vol. 56, nr 2, s. 175-181Artikel i tidskrift (Refereegranskat)
Abstract [en]

A reduction in the incidence of cardiovascular diseases (CVD) has been reported in the Western world, but post-infarction depression often occurs and is related to poor medical outcomes. The aim of this study was to examine the scientific literature by a systematic review, in order to find evidence for whether physical activity can be a tool to reduce depression in patients who have suffered a cardiac event. Three databases were systematically searched (PubMed, CINAHL, and Cochrane), and the GRADE protocol was used in combination with a revised Amstar-protocol for the systematic review. Scientific reports fitting the area were scarce. Finally, ten studies were included in this study: one meta-analysis, five randomized controlled trials, and four clinical trials. The results showed low to moderate evidence for the use of low to moderate levels of exercise as a tool to reduce depression in post-coronary artery event patients. This study concluded positive effects of physical activity as a tool to reduce depression in post-coronary artery event patients. Physiotherapists could be further involved in increasing physical activity after cardiac events. More studies are needed in the area.

Ort, förlag, år, upplaga, sidor
John Wiley & Sons, 2015
Nyckelord
Aerobic exercise, depression, myocardial infarction, physical activity
Nationell ämneskategori
Medicin och hälsovetenskap
Identifikatorer
urn:nbn:se:mau:diva-14593 (URN)10.1111/sjop.12190 (DOI)000351217500008 ()25756318 (PubMedID)2-s2.0-84925128129 (Scopus ID)20015 (Lokalt ID)20015 (Arkivnummer)20015 (OAI)
Tillgänglig från: 2020-03-30 Skapad: 2020-03-30 Senast uppdaterad: 2024-02-05Bibliografiskt granskad
Örmon, K., Torstensson Levander, M., Bahtsevani, C. & Sunnqvist, C. (2015). The life course of women who have experienced abuse: a life chart study in general psychiatric care (ed.). Journal of Psychiatric and Mental Health Nursing, 22(5), 316-325
Öppna denna publikation i ny flik eller fönster >>The life course of women who have experienced abuse: a life chart study in general psychiatric care
2015 (Engelska)Ingår i: Journal of Psychiatric and Mental Health Nursing, ISSN 1351-0126, E-ISSN 1365-2850, Vol. 22, nr 5, s. 316-325Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Violence against women is a worldwide problem and has an impact on the lives of women and girls. The study aims to investigate the life course of women within psychiatric care who have experienced abuse. The women’s resources, stressful events, experience of abuse, perpetrators, mental ill health, and care and support throughout the life course are also highlighted. Eleven women who had all sought general psychiatric care in an urban area in Sweden participated. A computer software program was used for constructing life charts for each participant, and manifest content analysis was used to analyse the data. The women’s social status and resources differed, and some of them spoke of only experiencing few stressful events growing up, while others described a stressful childhood. All of the women had been abused sometime during their life course, and most of the perpetrators were known to the women. Even so, the women had seldom disclosed their childhood abuse. As adults, the women were diagnosed with psychiatric diagnoses, and suicidal behaviour increased. The life chart offers rich information and a broader picture of the life history of women who experienced abuse as well as constituting a tool useful for identifying women with experiences of abuse.

Ort, förlag, år, upplaga, sidor
John Wiley & Sons, 2015
Nyckelord
child abuse, Domestic violence, Intimate Partner violence, Time Geography, Life chart
Nationell ämneskategori
Medicin och hälsovetenskap
Identifikatorer
urn:nbn:se:mau:diva-15036 (URN)10.1111/jpm.12177 (DOI)000355247300005 ()25311151 (PubMedID)2-s2.0-84929952160 (Scopus ID)17913 (Lokalt ID)17913 (Arkivnummer)17913 (OAI)
Tillgänglig från: 2020-03-30 Skapad: 2020-03-30 Senast uppdaterad: 2024-02-05Bibliografiskt granskad
Örmon, K., Torstensson Levander, M., Sunnqvist, C. & Bahtsevani, C. (2014). The duality of suffering and trust: abused women's experiences of general psychiatric care: an interview study (ed.). Journal of Clinical Nursing, 23(15-16), 2303-2312
Öppna denna publikation i ny flik eller fönster >>The duality of suffering and trust: abused women's experiences of general psychiatric care: an interview study
2014 (Engelska)Ingår i: Journal of Clinical Nursing, ISSN 0962-1067, E-ISSN 1365-2702, Vol. 23, nr 15-16, s. 2303-2312Artikel i tidskrift (Refereegranskat)
Abstract [en]

Aims and objectives To elucidate how women subjected to physical, emotional and/or sexual abuse experience the care provided at a general psychiatric clinic after the disclosure of abuse. Background Violence against women is a major global public health issue, which has an impact on women's lives and mental health as well as generating frequent hospital admission. Design Qualitative design with an inductive approach. Methods Interviews with nine women who were recipients of general psychiatric care and had disclosed experiences of abuse to a member of staff were conducted. Qualitative inductive content analysis was used. Results The overall theme emerging from the narratives, ‘dependency as a reality containing a duality of suffering and trust,’ links the categories together. Each subcategory is presented in relation to the categories ‘being belittled,’ ‘being misinterpreted’ and ‘being cared for.’ Experiences of care as caring and noncaring were found in the narratives. Caring could include situations experienced as the women being acknowledged and listened to, situations where staff approached and supported the women in a sensitive way. Experiences of noncaring were when the abuse was disregarded, and when the women were not believed in, were left with burdens of guilt and were offended. A noncaring environment focused primarily on the diagnosis, and the experienced abuse was seen as secondary. Conclusions Abused women are subjected to psychiatric environments where staff are divided into groups of those who believed in and supported the abused women and those who regarded experiences of abuse as a secondary issue and focused on the mental disorder. Relevance to clinical practice This study provides knowledge of how abused women experience the care provided at a general psychiatric clinic after the disclosure of abuse.

Ort, förlag, år, upplaga, sidor
John Wiley & Sons, 2014
Nyckelord
abused women, disclosure of abuse, experiences, general psychiatric care, inductive content analysis, interview
Nationell ämneskategori
Medicin och hälsovetenskap
Identifikatorer
urn:nbn:se:mau:diva-15161 (URN)10.1111/jocn.12512 (DOI)000339431800024 ()24372702 (PubMedID)2-s2.0-84904390021 (Scopus ID)16755 (Lokalt ID)16755 (Arkivnummer)16755 (OAI)
Tillgänglig från: 2020-03-30 Skapad: 2020-03-30 Senast uppdaterad: 2024-02-05Bibliografiskt granskad
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