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Institute
Naturentfremdung
(2018)
Hintergrund: Im Zuge der weltweiten Flüchtlingsbewegungen ist in den letzten Jahren eine hohe Anzahl an geflüchteten Personen nach Deutschland gekommen. Laut amtlicher Statistik lebten Ende 2018 ca. 1.780.000 Schutzsuchende in Deutschland (Statistisches Bundesamt 2019). Der Anteil weiblicher Schutzsuchender beträgt ca. 37,4 Prozent. Zirka 51 Prozent der geflüchteten Frauen, die in Deutschland ankommen und Asyl beantragen, befinden sich im gebärfähigen Alter zwischen 15 und 45 Jahren (Statistisches Bundesamt 2019a; _b). Darüber, wie viele schutzsuchende Frauen schwanger eingereist sind oder zum Zeitpunkt ihres Aufenthaltes in der Erstaufnahmeeinrichtung schwanger geworden sind, liegen keine Daten vor. Ebenso fehlen bisher in Deutschland repräsentative gesundheitsbezogene Daten von Schutzsuchenden (Frank, Yesil-Jürgens & Razum et al. 2017). Insbesondere zu den gesundheitlichen Problemlagen und Bedürfnissen von schutzsuchenden Frauen im Bereich Schwangerschaft, Geburt und postpartaler Phase liegen keine Erkenntnisse vor (Bozorgmehr, Mohsenpour & Saure et al. 2016; Heslehurst, Brown & Pemu et al. 2018). Internationale Studien deuten allerdings darauf hin, dass die gesundheitsbezogene Bedarfslage schutzsuchender Frauen komplex ist (Gagnon, Zimbeck & Zeitlin et al. 2009;van den Akker & van Roosmalen 2016). Die systematische Identifizierung von Versorgungsbedarfen und eine bedarfsgerechte Versorgungsplanung sind deshalb derzeit kaum möglich (Mörath 2019). Aus rechtlicher Perspektive ist diese unbefriedigende Situation ebenfalls problematisch (Klotz 2018). Die Umsetzung des völkerrechtlich bindenden internationalen Rechts auf ein für sie [Anmerk. d. V. : die Person] erreichbares Höchstmaß an körperlicher und geistiger Gesundheit (BGBI. 1976), welches von Deutschland 1976 ratifiziert wurde, sowie des UN-Übereinkommens zur Beseitigung jeder Diskriminierung der Frau von 1979 (BGBI. 1985) und der in der EU-Richtlinie 2013/33/EU in Kapitel IV aufgeführten Bestimmungen für schutzbedürftige Personen erfordert für diese spezifische Personengruppe vielfache Bemühungen. Denn die Förderung und Verbesserung der sexuellen und reproduktiven Gesundheit bzw. Rechte von schutzsuchenden Frauen kann einen Beitrag zu ihrer gesellschaftlichen Integration nach sich ziehen (Janssens, Bosmans & Temmerman 2005). Zuzüglich zur rechtlichen Situation schutzsuchender Frauen gilt das Recht ihrer Kinder auf Gesundheit. Im Artikel 24 der UN-Kinderrechtskonvention (UN, Committee on the Rights of the Child 2013) ist dieses verankert und unterstreicht u. a. für die Vor- und Nachsorge relevante Versorgungsbereiche wie z. B. prä- und postnatale Versorgung der Mütter, Aufklärung über Gesundheit und Ernährung u. w. m. (Deutsches Institut für Menschenrechte 2017).
Problem: Familien in der ambulanten palliativen Situation unterliegen vielen Belastungen, welche bislang in Deutschland nur unzureichend erforscht wurden. Fragestellung: Wie kann die Situation von Familien in der ambulanten palliativen Betreuung auf Grundlage des aktuellen Forschungsstands für eine schriftliche Befragung in Deutschland konzeptualisiert werden? Methode: Basierend auf einer Literaturrecherche wurden Publikationen identifiziert, welche die Bedürfnisse und Belastungen der Familien untersuchten. Die Treffer wurden inhaltlich analysiert und kategorisiert. Auf dieser Grundlange wurden Instrumente recherchiert, welche die relevanten Kategorien adressieren. Die daraus ausgewählten Instrumente wurden zu einem Screeninginstrument zusammengefasst. Ergebnisse: Die 529 relevanten Publikationen beinhalten 38 Themengebiete in acht Kategorien. Hieraus wurde ein 71 Items umfassendes Screeninginstrument zusammengestellt, welches die palliative Situation der Familien in Deutschland erheben soll.
Hintergrund/ Antrag der Bundestagsfraktionen vom 08.11.2011:
Von den Fraktionen CDU/CSU, FDP, SPD und Die Linke wurde am 08.11.2011 ein Entschließungsantrag an den Deutschen Bundestag eingereicht, der sich gegen eine Anhebung der schulischen Anfor-derungen als Zugang zur Ausbildung in der allgemeinen Gesund-heits- und Krankenpflege sowie zur Hebamme/ Entbindungspfleger von zehn auf zwölf Schuljahre ausspricht. Begründet wird der An-trag mit der hohen Qualität der Ausbildung in diesen Bereichen, die eine Anhebung der Zugangsvoraussetzungen nach Ansicht der Antragsteller überflüssig macht. Zudem würde durch die Anhebung der schulischen Anforderungen der Kreis der potenziellen Bewerbe-rinnen und Bewerber eingeschränkt und dadurch der Fachkräfte-mangel in der Pflege verschärft. Der Antrag wurde am 9.11.2011 im Ausschuss „Gesundheit“ des Bundestages verabschiedet.
Background
Lay family caregivers of patients receiving palliative care often confront stressful situations in the care of their loved ones. This is particularly true for families in the home-based palliative care settings, where the family caregivers are responsible for a substantial amount of the patient’s care. Yet, to our knowledge, no study to date has examined the family caregivers’ exposure to critical events and distress with home-based palliative care has been reported from Germany. Therefore, we attempt to assess family caregiver exposure to the dying patient’s critical health events and relate that to the caregiver’s own psychological distress to examine associations with general health within a home-based palliative care situation in Germany.
Methods
A cross-sectional study was conducted among 106 family caregivers with home-based palliative care in the Federal State of North Rhine Westphalia, Germany. We administered the Stressful Caregiving Adult Reactions to Experiences of Dying (SCARED) Scale. Descriptive statistics and linear regression models relating general health (SF-36) were used to analyze the data.
Results
The frequency of the caregiver’s exposure, or witness of, critical health events of the patient ranged from 95.2% “pain/discomfort” to 20.8% “family caregiver thought patient was dead”. The highest distress scores assessing fear and helpfulness were associated with “family caregiver felt patient had enough’” and “family caregiver thought patient was dead”. Linear regression analyses revealed significant inverse associations between SCARED critical health event exposure frequency (beta = .408, p = .025) and total score (beta = .377, p = .007) with general health in family caregivers.
Conclusions
Family caregivers with home-based palliative care in Germany frequently experience exposure to a large number of critical health events in caring for their family members who are terminally ill. These exposures are associated with the family caregiver’s degree of fear and helplessness and are associated with their worse general health. Thus the SCARED Scale, which is brief and easy to administer, appears able to identify these potentially upsetting critical health events among family caregivers of palliative care patients receiving care at home. Because it identified commonly encountered critical events in these patients and related them to adverse general health of family caregivers, the SCARED may add to clinically useful screens to identify family caregivers who may be struggling.
Aim: The aim of this study was to give an overview of family caregiver satisfaction within the home palliative care situation in North Rhine-Westphalia, Germany.
Design: A cross-sectional study.
Methods: An anonymous questionnaire, with seven validated scales, and comprising of 71 items, was used. The items investigated perceived needs and burdens of families within a home-based palliative care situation.
The satisfaction of the family caregivers with the services delivered by palliative care teams was measured by the FAMCARE-2 Scale. Descriptive statistics and analysis of covariance (ANCOVA) were performed.
Results: A convenience sample of 106 family members agreed to participate in the study. Overall, we found high satisfaction within our sample. There was high satisfaction with how the services respected the dignity of families, and how they provided comfort to patients. Satisfaction was lower with regard to information about patients.
Conclusion: High or low satisfaction with palliative care, tells us little about the quality of services. The high satisfaction within this study could be interpreted as a sign that palliative care was important to families at the time of availability. Regular and continuous assessment can serve to inform the continuous quality of care provision for patients and their families.
Background
Forced migration significantly endangers health. Women face numerous health risks, including sexual violence, lack of contraception, sexually transmitted disease, and adverse perinatal outcomes. Therefore, sexual and reproductive healthcare is a significant aspect of women asylum seekers’ health.
Even when healthcare costs of asylum seekers are covered by the government, there may be strong barriers to healthcare access and specific needs may be addressed inadequately. The study’s objectives were a) to assess the accommodation and healthcare services provided to women asylum seekers in standard and specialised health care, b) to assess the organisation of healthcare provision and how it addresses the sexual and reproductive healthcare needs of women asylum seekers.
Methods
The study utilised a multi-method approach, comprising a less-dominant quantitative component and dominant qualitative component. The quantitative component assessed accommodation conditions for women in eight asylum centres using a survey. The qualitative component assessed healthcare provision on-site, using semi-structured interviews with health and social care professionals (n = 9). Asylum centres were selected to cover a wide range of characteristics. Interview analysis was guided by thematic analysis.
Results
The accommodation in the asylum centres provided gender-separate rooms and sanitary infrastructure. Two models of healthcare were identified, which differed in the services they provided and in their organisation: 1) a standard healthcare model characterised by a lack of coordination between healthcare providers, unavailability of essential services such as interpreters, and fragmented healthcare, and 2) a specialised healthcare model specifically tailored to the needs of asylum-seekers. Its organisation is characterised by a network of closely collaborating health professionals. It provided essential services not present in the standard model. We recommend the specialised healthcare model as a guideline for best practise.
Conclusions
The standard, non-specialised healthcare model used in some regions in Switzerland does not fully meet the healthcare needs of women asylum seekers. Specialised healthcare services used in other regions, which include translation services as well as gender and culturally sensitive care, are better suited to address these needs. More widespread use of this model would contribute significantly toward protecting the sexual and reproductive integrity and health of women asylum seekers.
Die Fachhochschule (FH) Osnabrück hat eine sehr lange Geschichte in der Akademisierung der Gesundheitsberufe. Bereits in den 1990er Jahren wurde damit begonnen, die ersten Studienprogramme für die Pflege bzw. für das Pflege- und das Gesundheitsmanagement sowie für die Ergo-, Logo- und Physiotherapie zu entwickeln. Im Wintersemester 2008/09 kam das bundesweit erste ausbildungsergänzende Bachelorstudienprogramm für Hebammen hinzu.
Background
This study describes a low-cost and time-efficient clinical sensory test (CST) battery and evaluates its concurrent validity as a screening tool to detect somatosensory dysfunction as determined using quantitative sensory testing (QST).
Method
Three patient cohorts with carpal tunnel syndrome (CTS, n = 76), non-specific neck and arm pain (NSNAP, n = 40) and lumbar radicular pain/radiculopathy (LR, n = 26) were included. The CST consisted of 13 tests, each corresponding to a QST parameter and evaluating a broad spectrum of sensory functions using thermal (coins, ice cube, hot test tube) and mechanical (cotton wool, von Frey hairs, tuning fork, toothpicks, thumb and eraser pressure) detection and pain thresholds testing both loss and gain of function. Agreement rate, statistical significance and strength of correlation (phi coefficient) between CST and QST parameters were calculated.
Results
Several CST parameters (cold, warm and mechanical detection thresholds as well as cold and pressure pain thresholds) were significantly correlated with QST, with a majority demonstrating >60% agreement rates and moderate to relatively strong correlations. However, agreement varied among cohorts. Gain of function parameters showed stronger agreement in the CTS and LR cohorts, whereas loss of function parameters had better agreement in the NSNAP cohort. Other CST parameters (16 mN von Frey tests, vibration detection, heat and mechanical pain thresholds, wind-up ratio) did not significantly correlate with QST.
Conclusion
Some of the tests in the CST could help detect somatosensory dysfunction as determined with QST. Parts of the CST could therefore be used as a low-cost screening tool in a clinical setting.
Significance
Quantitative sensory testing, albeit considered the gold standard to evaluate somatosensory dysfunction, requires expensive equipment, specialized examiner training and substantial time commitment which challenges its use in a clinical setting. Our study describes a CST as a low-cost and time-efficient alternative. Some of the CST tools (cold, warm, mechanical detection thresholds; pressure pain thresholds) significantly correlated with the respective QST parameters, suggesting that they may be useful in a clinical setting to detect sensory dysfunction.
This review aimed to synthesize the current evidence on the effectiveness of invasive treatments for complex regional pain syndrome in children and adolescents. Studies on children and adolescents with complex regional pain syndrome that evaluated the effects of invasive treatment were identified in PubMed (search March 2013). Thirty-six studies met the inclusion criteria. Articles reported on a total of 173 children and adolescents with complex regional pain syndrome. Generally, many studies lack methodological quality. The invasive treatments applied most often were singular sympathetic blocks, followed by epidural catheters and continuous sympathetic blocks. Rarely, spinal cord stimulation and pain-directed surgeries were reported. An individual patient frequently received more than one invasive procedure. Concerning outcome, for approximately all patients, an improvement in pain and functional disability was reported. However, these outcomes were seldom assessed with validated tools. In conclusion, the evidence level for invasive therapies in the treatment of complex regional pain syndrome in children and adolescents is weak.
Seit der Trennung von ihrem Freund klagt die 32-jährige Anne über morgendliche Kopfschmerzen, Parästhesien am Hinterkopf, Schwindel und verspannte Kiefermuskeln. Lange bleibt für ihren Hausarzt, die Psychologin und Physiotherapeut Professor Harry von Piekartz unklar, was die Symptome auslöst. Denn der Unruhestifter ist unsichtbar.
Ludwig ist irritiert. Auf seiner rechten Schulter hat sich eine sichtbare Beule entwickelt, die vor allem am Schreibtisch Schmerzen auslöst. Seinem Hobby, dem Kickboxen, kann er glücklicherweise noch nachgehen. Da die Beule weiter wächst und ihn seine Freundin darauf aufmerksam macht, dass er seinen Kopf schief hält, geht er zum Arzt und schließlich zu Physiotherapeut Prof. Dr. Harry von Piekartz.
Das 10-jährige Bestehen physiotherapeutischer Studiengänge in Deutschland gibt Gelegenheit, Bilanz zu ziehen und die weitere Entwicklung zu überlegen. Der Artikel soll insbesondere auch jungen Kollegen Orientierung darüber geben, was es mit den verschiedenen Programmen und Abschlüssen auf sich hat und auf welche Qualitätsmerkmale zu achten ist.
Hintergrund:
Im Kontext einer zunehmenden öffentlichen Aufmerksamkeit für das Thema Forschung in Gesundheitsfachberufen rückt die Frage in den Vordergrund, wie Forschungsaktivitäten im Bereich der Physiotherapie forciert werden können. Auch wenn es kein generelles Erfolgsrezept gibt, wird die Erfolg versprechende Formulierung von Forschungsanträgen im Dschungel der Fördermöglichkeiten zunehmend zu einer elementaren Kompetenz des Forschers.
Ziel/Methode:
Ziel des Beitrags ist es, den aktuellen Stand des Themas Forschung in Gesundheitsfachberufen – insbesondere in der Physiotherapie – aufzuzeigen und mithilfe von konkreten Hinweisen im Erstellungsprozess die Erfolgsaussichten eines Antrags zur Forschungsförderung zu erhöhen.
Ergebnis/Schlussfolgerung:
Sowohl Erfolgsvariablen als auch Gründe für das Scheitern eines Antrags lassen sich bestimmen. Insgesamt ist das Formulieren von Forschungsanträgen allerdings ein ständiger Lernprozess – in diesem Zusammenhang ist Erfolg ein relativer Begriff.
Currently, the treatment of musicians is an interprofessional approach. Playing-related health complaints may impact the performance of a musician. In Germany, a medical consulting hour for musicians exists, but those for athletes in sports medicine are not so common. The diagnosing and treatment procedure within the physiotherapy consultation for musicians follows a specific concept-b and requires knowledge of instruments and musician-specific complaints. Based on the consulting hour in a clinic in Osnabrueck, 614 case reports were part of this sample, of which 558 data sets were complete. The focus of the analysis is the instrument and the primary complaint. Also, the type of therapy is characterized, and the amount is calculated. Primary complaints of musicians, in general, are found most frequently in the spine and upper extremity. Musician complaints are different between instruments. Instrumentalists have a significantly higher chance to suffer from a primary complaint in the area of the upper extremity. Furthermore, the groups without an instrument (e.g., singing or dancing) are developing complaints in the anatomical area which they primarily use. Therefore, these types of therapy were used: physiotherapy, manual therapy, and osteopathy with an average of 5.9 treatment units. This study underpinned the importance of musician-specific physiotherapy as a profession to treat musicians. Also, an interdisciplinary approach is necessary to treat all aspects of complaints.
Wer eine Physiotherapiezeitschrift von Thieme abonniert hat, kann damit künftig Fortbildungspunkte sammeln. Regel-mäßig wird es sogenannte CPTE-Artikel samt Fragen geben, die man online beantworten kann. Der Artikel erzählt den Weg der Forschungsgruppe, die sich mit Continuing Physiotherapy Education beschäftigt.
Wer eine Physiotherapiezeitschrift von Thieme abonniert hat, kann damit künftig Fortbildungspunkte sammeln. Regelmäßig wird es sogenannte CPTE-Artikel samt Fragen geben, die man online beantworten kann. Der Artikel erzählt den Weg der Forschungsgruppe, die sich mit Continuing Physiotherapy Education beschäftigt.
Obwohl sich die Anforderungen im Sport und dem Musizieren ähneln, ist die Musikerphysiotherapie längst nicht so entwickelt wie die Sportphysiotherapie. Dabei lassen sich die sogenannten „Performance-Related Musculoskeletal Disorders“ erfolgreich mit Manueller Therapie oder Physiotherapie, z. B. mit Hilfe einer Bewegungsanalyse, therapieren. Prof. Dr. med. Christoff Zalpour gibt einen Überblick über das Feld der Musikerphysiotherapie, deren Potenzial noch lange nicht vollends erschlossen ist.
Um den Anforderungen eines Erstkontaktes in der Physiotherapie gerecht zu werden, ist es unerlässlich, internistische oder viszerale Erkrankungen zu (er)kennen, die sich hinter muskuloskelettalen Symptomen verbergen können. Dr. Christoff Zalpour stellt die häufigsten Erkrankungen und ihre Symptome vor.
Physiotherapie in Kirgisien
(2010)
Bericht der 23. ENPHE-Konferenz in Riga : Grenzenlose Transparenz in der Physiotherapieausbildung
(2010)
Introduction Postoperative delirium (POD) is seen in approximately 15% of elderly patients and is related to poorer outcomes. In 2017, the Federal Joint Committee (Gemeinsamer Bundesausschuss) introduced a ‘quality contract’ (QC) as a new instrument to improve healthcare in Germany. One of the four areas for improvement of in-patient care is the ‘Prevention of POD in the care of elderly patients’ (QC-POD), as a means to reduce the risk of developing POD and its complications.
The Institute for Quality Assurance and Transparency in Health Care identified gaps in the in-patient care of elderly patients related to the prevention, screening and treatment of POD, as required by consensus-based and evidence-based delirium guidelines. This paper introduces the QC-POD protocol, which aims to implement these guidelines into the clinical routine. There is an urgent need for well-structured, standardised and interdisciplinary pathways that enable the reliable screening and treatment of POD. Along with effective preventive measures, these concepts have a considerable potential to improve the care of elderly patients.
Methods and analysis The QC-POD study is a non-randomised, pre–post, monocentric, prospective trial with an interventional concept following a baseline control period. The QC-POD trial was initiated on 1 April 2020 between Charité-Universitätsmedizin Berlin and the German health insurance company BARMER and will end on 30 June 2023. Inclusion criteria: patients 70 years of age or older that are scheduled for a surgical procedure requiring anaesthesia and insurance with the QC partner (BARMER). Exclusion criteria included patients with a language barrier, moribund patients and those unwilling or unable to provide informed consent. The QC-POD protocol provides perioperative intervention at least two times per day, with delirium screening and non-pharmacological preventive measures.
Ethics and dissemination This protocol was approved by the ethics committee of the Charité-Universitätsmedizin, Berlin, Germany (EA1/054/20). The results will be published in a peer-reviewed scientific journal and presented at national and international conferences.