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  • 1
    In: American Journal of Hospice and Palliative Medicine®, SAGE Publications, Vol. 36, No. 6 ( 2019-06), p. 492-499
    Abstract: In Germany, some units of specialized palliative care (SPC) offer a 6- to 12-month rotation for resident physicians (RPs) and fellows from different specialties. Objective: This pilot study aimed to evaluate feasibility of assessing palliative care knowledge (PCK) and palliative care self-efficacy (PCSE) using a paper-based questionnaire. Methods: Palliative care knowledge and PCSE were assessed by introducing a score, followed by a descriptive analysis (determination of frequency, mean, median, and range) using nonparametric tests (χ 2 test, Mann–Whitney U test). Results: We assessed 17 RPs following SPC rotation and 16 board-certified specialists (BCSs) who had no experience in SPC from 3 German comprehensive cancer centers. Resident physicians were predominantly enrolled in residency programs of hematology and oncology (n = 6), anesthesiology (n = 6), and psychosomatic medicine (n = 3). Resident physicians rotated between year 1 and 8 of residency. Fifteen RPs (88%) had elected this rotation and 72% preferred 12-month duration. The total PCK score of PCK was 27 (RPs) and 24 (BCSs; P = .002). Mean PCSE scores were 46 (RPs) and 39 (BCSs; P = .016). Of 71% of RPs, only 27% of BCSs knew how support of hospice service was initiated ( P = .004). Participants rated the items as comprehensible (n = 24; 73%), relevant (n = 25; 76%) and the questionnaire as adequately long (n = 23; 70%). Conclusion: An improved PCK and PCSE were observed in physicians who rotated through an SPC unit; this resulted in an increased tangibility of local palliative care and hospice services. The questionnaire was comprehensible, relevant in terms of content, and adequate in length for a prospective multicenter survey.
    Type of Medium: Online Resource
    ISSN: 1049-9091 , 1938-2715
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2019
    detail.hit.zdb_id: 2236674-X
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  • 2
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2020
    In:  Supportive Care in Cancer Vol. 28, No. 9 ( 2020-09), p. 4539-4539
    In: Supportive Care in Cancer, Springer Science and Business Media LLC, Vol. 28, No. 9 ( 2020-09), p. 4539-4539
    Type of Medium: Online Resource
    ISSN: 0941-4355 , 1433-7339
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2020
    detail.hit.zdb_id: 1463166-0
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  • 3
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2003
    In:  Supportive Care in Cancer Vol. 11, No. 7 ( 2003-7-1), p. 442-451
    In: Supportive Care in Cancer, Springer Science and Business Media LLC, Vol. 11, No. 7 ( 2003-7-1), p. 442-451
    Type of Medium: Online Resource
    ISSN: 0941-4355 , 1433-7339
    Language: Unknown
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2003
    detail.hit.zdb_id: 1463166-0
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  • 4
    Online Resource
    Online Resource
    Georg Thieme Verlag KG ; 2019
    In:  DMW - Deutsche Medizinische Wochenschrift Vol. 144, No. 23 ( 2019-11), p. e153-e159
    In: DMW - Deutsche Medizinische Wochenschrift, Georg Thieme Verlag KG, Vol. 144, No. 23 ( 2019-11), p. e153-e159
    Abstract: Hintergrund Ein Palliativdienst ist in der Beratung und Versorgung von Patienten mit einer Tumorerkrankung als Qualitätsindikator anerkannt und in National Cancer Institutes, Vorbild der deutschen Comprehensive Cancer Center (CCC), flächendeckend (92 %) umgesetzt. Daher stellt sich die Frage, wie die Palliativdienste aktuell in die CCCs integriert sind. Methode Durch eine papierbasierte quantitative Befragung an 16 Standorten der bisher geförderten CCCs wurden von Juli bis August 2017 Angaben zum Vorhandensein, zur personellen Situation, Inanspruchnahme und zu Perspektiven eines Palliativdienstes erfasst. Die Befragung richtete sich an die Leiter der palliativmedizinischen Einheiten der CCCs. Die Daten wurden in SPSS ausgewertet (Häufigkeit, Median, Mittelwert, Spannweite). Ergebnisse 15 CCCs haben an der Befragung teilgenommen (Rücklauf 94 %). 13 der 15 CCCs verfügen über einen Dienst, der Palliativpatienten mitbehandelt. In 12 von 13 CCCs sind diese in den Regelarbeitszeiten (wochentags 8–16 Uhr) erreichbar. Alle Dienste sind ärztlich besetzt, 11 zusätzlich pflegerisch. 7 Dienste sind neben Arzt und Pflege mit einer weiteren Profession besetzt. Es wurden im Jahr 2016 im Median 4482 Mitbehandlungen durch die Dienste erbracht, davon 80 % als Zusatzentgelte (ZE) ohne Erlös und ohne kodierbaren OPS. Im Jahr 2017 planen 5 Zentren das ZE 2017-133, 2 Zentren das ZE 60 und 3 Zentren beide ZE abzurechnen. Diskussion Dienste für Palliativpatienten sind in den deutschen CCCs regelhaft vorhanden, erfüllen jedoch nur zur Hälfte die in der S3-Leitlinie geforderte Bedingung der Multiprofessionalität. Das im Jahr 2017 neu eingeführte, stundengenau abrechenbare Zusatzentgelt könnte hier Verbesserungen schaffen und zur Kostendeckung beitragen. Dadurch können entgegen der bisherigen Regelung notwendige und sinnvolle Leistungen mit einer Behandlungsdauer auch unter 7 Tagen abgerechnet werden.
    Type of Medium: Online Resource
    ISSN: 0012-0472 , 1439-4413
    RVK:
    RVK:
    Language: German
    Publisher: Georg Thieme Verlag KG
    Publication Date: 2019
    detail.hit.zdb_id: 2035474-5
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  • 5
    In: Palliative Medicine, SAGE Publications, Vol. 18, No. 2 ( 2004-03), p. 100-107
    Abstract: The development of palliative medicine in inpatient units in Germany has been impressive in the last years. As a first step of quality assurance, a core documentation form was developed in 1996. In 2001, 55 of the 83 palliative inpatient units in Germany and one unit each in Switzerland and Austria participated in the third phase of the evaluation of the core documentation. A total of 1304 patients were documented consecutively in the 57 units for a period of up to three months. This study investigates the frequency of drugs used in palliative care units in Germany. During inpatient treatment, the most common drug classes were strong opioids (68% of the patients), nonopioids (59%), corticosteroids (32%), laxatives (31%), antiemetics (27%), gastric protection agents (24%), neuroleptics (19%), sedatives/anxiolytics (18%), antidepressants (16%) and diuretics (15%). These ten drug classes made up for 72% of all prescriptions in the palliative care units. The substances used most frequently were dipyrone (47% of the patients), morphine (42%), fentanyl (28%), dexamethasone (27%), metoclopramide (21%), sodium picosulfate (15%), haloperidol (13%), pantoprazole (11%), macrogol (11%), amtriptyline (11%), furosemide (10%), omeprazole (9%), lactulose (8%), rofecoxib (8%) and lorazepam (7%). The 15 most commonly used drugs accounted for 54% of the prescriptions in the palliative care units in Germany. Drug treatment was related to sex, age and functional status of the patients. Patients who died in a palliative care unit had received significantly more frequent doses of neuroleptics (PB / 0.001), corticosteroids (PB / 0.001), sedatives/anxiolytics (PB / 0.001) and strong opioids (PB / 0.001). This study is the first representative and systematic evaluation of drug treatment in palliative care units in a European country. Many of the ’top 15‘ drugs were drugs included in the list of essential drugs of the World Health Organisation though availability and cultural differences have an effect on the use of drugs, e.g., the high usage of dipyrone in Germany. Age and sex-related differences in drug therapy were seen, and more research is needed to recognize possible undertreatment of symptoms in subgroups of patients, e.g., treatment of depression in older or male patients.
    Type of Medium: Online Resource
    ISSN: 0269-2163 , 1477-030X
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2004
    detail.hit.zdb_id: 2027566-3
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  • 6
    In: Palliative Medicine, SAGE Publications, Vol. 27, No. 1 ( 2013-01), p. 84-90
    Abstract: For palliative care settings, little is known about the benefits of specific methicillin-resistant Staphylococcus aureus containment regimens and the burdens patient isolation imposes on affected patients, their families, and professional caregivers. Aim: To explore the current practice of MRSA management and its impact on inpatients’ quality of life as perceived by professional caregivers. Design: Survey of inpatient palliative care institutions using 23-item questionnaires (infrastructural data: six items, management process: 14, clinical significance: three). Setting/participants: All palliative care units (179) and hospices (181) listed in Germany’s directory of palliative care services. The χ 2 test was used to test for differences; significance level: p ≤ 0.05. Results: 229 of 360 questionnaires were returned. More than 90% of the responding institutions employed specific MRSA protocols. Lack of resources was a more important issue for palliative care units than for hospices regarding availability of single rooms ( p = 0.002) and staffing ( p = 0.004). Compared to hospices, palliative care units more frequently isolated MRSA patients ( p = 0.000), actively treated colonization ( p = 0.026), assessed the efficacy of eradication ( p = 0.000), provided information on MRSA management to patients ( p = 0.014) and relatives ( p = 0.001), more often restricted patients’ activities ( p = 0.000), and reported a negative impact on quality of life ( p = 0.000). Conclusions: Rigorously applied MRSA protocols impose significant burdens at the end of life. Research on clinical outcomes including quality of life may identify interventions of questionable benefit. The issue of handling MRSA should be studied as a model for the management of other highly complex conditions and special needs such as patient isolation.
    Type of Medium: Online Resource
    ISSN: 0269-2163 , 1477-030X
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2013
    detail.hit.zdb_id: 2027566-3
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  • 7
    Online Resource
    Online Resource
    Walter de Gruyter GmbH ; 2010
    In:  Zeitschrift für wirtschaftlichen Fabrikbetrieb Vol. 105, No. 9 ( 2010-09-28), p. 785-790
    In: Zeitschrift für wirtschaftlichen Fabrikbetrieb, Walter de Gruyter GmbH, Vol. 105, No. 9 ( 2010-09-28), p. 785-790
    Abstract: Faserverbundwerkstoffe werden auf Grund ihres hohen Leichtbaupotenzials immer häufiger für technische Produkte verwendet. Die hohen spezifischen Herstellkosten der Bauteile, für die noch keine großserientauglichen Produktionsprozesse bekannt sind, schränken aktuell die weitere Verbreitung dieser Technologie in unterschiedlichen Anwendungsfeldern ein. Im vorliegenden Artikel wird ein Ansatz vorgestellt, bei dem die RFID-Technologie genutzt wird, um Herstellungsprozesse von Faserverbundwerkstoffen durch ein effizientes Informationsmanagement zu verbessern. Dabei werden RFID-Transponder bauteilspezifisch eingesetzt und können über den gesamten Lebenszyklus des Bauteils, beispielsweise zum Zwecke der Produktionssteuerung, Prozessregelung oder zur Bauteilrückverfolgung, eingesetzt werden.
    Type of Medium: Online Resource
    ISSN: 2511-0896 , 0947-0085
    RVK:
    RVK:
    Language: English
    Publisher: Walter de Gruyter GmbH
    Publication Date: 2010
    detail.hit.zdb_id: 2133068-2
    detail.hit.zdb_id: 1225290-6
    SSG: 3,2
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  • 8
    Online Resource
    Online Resource
    Walter de Gruyter GmbH ; 2011
    In:  ZWF Zeitschrift für wirtschaftlichen Fabrikbetrieb Vol. 106, No. 11 ( 2011-11-28), p. 838-843
    In: ZWF Zeitschrift für wirtschaftlichen Fabrikbetrieb, Walter de Gruyter GmbH, Vol. 106, No. 11 ( 2011-11-28), p. 838-843
    Type of Medium: Online Resource
    ISSN: 0947-0085 , 2511-0896
    RVK:
    RVK:
    Language: German
    Publisher: Walter de Gruyter GmbH
    Publication Date: 2011
    detail.hit.zdb_id: 2133068-2
    detail.hit.zdb_id: 1225290-6
    SSG: 3,2
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  • 9
    Online Resource
    Online Resource
    SAGE Publications ; 2018
    In:  American Journal of Hospice and Palliative Medicine® Vol. 35, No. 7 ( 2018-07), p. 1023-1029
    In: American Journal of Hospice and Palliative Medicine®, SAGE Publications, Vol. 35, No. 7 ( 2018-07), p. 1023-1029
    Abstract: Patient-reported outcomes are usually considered to be the gold standard assessment. However, for the assessment of quality of dying and death, ratings of informal caregivers (ICGs) or health-care professionals (HCPs) must be considered for ethical and methodological reasons. This article aims to present results of ICGs’ and HCPs’ estimates of the questionnaire, quality of dying and death (QoDD) on patients who died in PCUs and to compare the level of agreement of both ratings/raters. Methods: The parent validation study to this analysis assessed the ICG and HCP versions of the QoDD. Descriptive statistics are presented for each item in both versions. T tests for the estimation of differences between ICG and HCP were performed. Case-related absolute differences between estimates were analyzed regarding the extent of agreement and deviation. Results: Two hundred fifteen matched ICG and HCP ratings were analyzed. The ratings in all 6 QoDD dimensions were high; single items scored low. Mean absolute difference between both ratings was 0.33 (standard deviation [SD]: 3.08; median 0.05) on a 0 to 10 numerical rating scale and ranges between −8.24 (higher rating of ICGs compared to HCPs) and 9.33 (higher rating of HCPs compared to ICGs). Conclusions: The findings appear to show a high satisfaction with quality of dying and death as rated by ICGs and HCPs, but we suspect this might be indicative of a methodological challenge, that is, a ceiling effect in both assessments. Single low scoring items may provide important clues for improvement in end-of-life care. Although descriptive data show comparable mean values and standard deviations, the actual congruence of ratings is low. In summary, replacing one rating by another cannot be recommended.
    Type of Medium: Online Resource
    ISSN: 1049-9091 , 1938-2715
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2018
    detail.hit.zdb_id: 2236674-X
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  • 10
    Online Resource
    Online Resource
    SAGE Publications ; 2016
    In:  American Journal of Hospice and Palliative Medicine® Vol. 33, No. 8 ( 2016-09), p. 760-769
    In: American Journal of Hospice and Palliative Medicine®, SAGE Publications, Vol. 33, No. 8 ( 2016-09), p. 760-769
    Abstract: To validate the Quality of Dying and Death (QoDD) instrument for health professionals (QoDD-D-MA) and to test its feasibility in 2 German palliative care units (PCUs). Methods: The QoDD was translated from English to German and then retranslated following European Organisation for Research and Treatment of Cancer (EORTC) guidelines. Data were collected in 2 German PCUs to calculate aspects of validity and reliability. Results: Mean total score was 83.05 (range 49-100; N = 232). The QoDD-D-MA showed satisfactory psychometric properties, Cronbach α = .830; interrater reliability r = .245 ( P 〈 .01). The QoDD-D-MA was independent of patients’ demographic and clinical aspects. Some challenges occurred when applying the instrument. Conclusions: Feasibility could be improved by adapting the QoDD-D-MA to create a self-assessment version and finding a solution for items that result in many missing data. Future research should validate the QoDD-D-MA in other care settings.
    Type of Medium: Online Resource
    ISSN: 1049-9091 , 1938-2715
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2016
    detail.hit.zdb_id: 2236674-X
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