Gotowe bibliografie tematyczne / Patient

Gotowa bibliografia na temat „Patient”

Autor: Grafiati
Data publikacji: 4 czerwca 2021
Data aktualizacji: 29 lipca 2024

Utwórz poprawne odniesienie w stylach APA, MLA, Chicago, Harvard i wielu innych

Wybierz rodzaj źródła:

Spis treści

Zobacz listy aktualnych artykułów, książek, rozpraw, streszczeń i innych źródeł naukowych na temat „Patient”.

Przycisk „Dodaj do bibliografii” jest dostępny obok każdej pracy w bibliografii. Użyj go – a my automatycznie utworzymy odniesienie bibliograficzne do wybranej pracy w stylu cytowania, którego potrzebujesz: APA, MLA, Harvard, Chicago, Vancouver itp.

Możesz również pobrać pełny tekst publikacji naukowej w formacie „.pdf” i przeczytać adnotację do pracy online, jeśli odpowiednie parametry są dostępne w metadanych.

Artykuły w czasopismach na temat "Patient"

1

B N, Beena Ullala Mata, Rameshwara G N, Naveen Kumar G i Raghavendra B. "Effects of Computerized Patient Records on Patients". Bonfring International Journal of Man Machine Interface 3, nr 3 (31.07.2015): 25–29. http://dx.doi.org/10.9756/bijmmi.8068.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
2

Jamil, Waqas, Abdullah Alahwal, Ravinder Suman, Megan Whitwell, Farah Naz i Thomas Beech. "Do Patients Correctly Use Steroid Nose Spray? A Patient-Reported Survey of the Nasal Spray Technique and Patient Compliance". Journal of Clinical Otorhinolaryngology 3, nr 4 (4.11.2021): 01–05. http://dx.doi.org/10.31579/2692-9562/033.

Pełny tekst źródła
Streszczenie:
Background:Correct nasal spray techniqueand patient compliance are the two mostimportant factors in the use of steroid nose spray. Objectives:To find out if patientsuse steroid nasal spray with a correctspray technique and if they are compliant in using the spray. Design: Patient-reported survey Participants: 100 participants (1 excluded) Main outcome measures 1) Nasal spray technique 2) Patient compliance Results: Out of 99 participants included in this study only one patient used steroid nose spray with a completely correct spray technique. 40% of patients received guidance instructions from the prescriber about the spray technique. 70% of patients reported using their spray regularly and 53% of patients were found using the correct dosage of the spray. Conclusions: Wrong spray technique and patient noncompliance is common and can be corrected. This survey emphasizes the importance of giving written and verbal instructions about the use of spray to the patients.
Style APA, Harvard, Vancouver, ISO itp.
3

Harpham, Wendy S. "Patient Patients". Oncology Times 30, nr 24 (grudzień 2008): 31. http://dx.doi.org/10.1097/01.cot.0000343806.22728.bf.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
4

Koch, Amelie, Nikoloz Gambashidze i Matthias Weigl. "Einbeziehung von Patient:innen zur Förderung von Patientensicherheit in Gesund-heitseinrichtungen in Deutschland". Monitor Versorgungsforschung 16, nr 06 (2.12.2023): 74–78. http://dx.doi.org/10.24945/mvf.06.23.1866-0533.2567.

Pełny tekst źródła
Streszczenie:
Background: Proactive involvement of patients in the design of safe care is a WHO-defined goal of the current decade. This paper investigated (a) which patient involvement activities and measures are implemented in German health care facilities for patient safety, and (b) which recommendations for action can be derived for our health care facilities. Aim and method: A literature and Internet search was conducted on institutional practices and organizational activities in Germany to improve patient safety with the involvement of patients. Interviews with five experts were conducted who advised our approach. An agenda for future research projects and first recommendations for clinical practice was formulated afterwards. Results: The evidence base on established measures to incorporate patient perspectives into the strategic promotion of patient safety in healthcare facilities in Germany is scarce and inconsistent. Patient surveys and the use of patient advocates are common. It remains unclear how patient councils as well as self-help groups have the potential to contribute to the promotion of patient safety in practice. Conclusions and agenda: An agenda is proposed. A more in-depth empirical survey and description of the situation in Germany, taking into account the experience of experts from clinical practice, is necessary to obtain a complete picture of the currently established measures for patient involvement, to uncover potential for realization and to define necessary framework conditions.
Style APA, Harvard, Vancouver, ISO itp.
5

劉庭維, 劉庭維. "家屬拒絕病患插管案：從病人自主權至病人善終權". 月旦醫事法報告 93, nr 93 (lipiec 2024): 081–103. http://dx.doi.org/10.53106/241553062024070093007.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
6

Widjaja, Herry Prabowo Krestiyanto. "Assessment of Patient Satisfaction Among Pregnant Patients in The Out-Patient Department of Obstetrics and Gynecology Section at Metropolitan Medical Center Manila". Jurnal Manajemen Kesehatan Indonesia 8, nr 3 (27.12.2020): 148–52. http://dx.doi.org/10.14710/jmki.8.3.2020.148-152.

Pełny tekst źródła
Streszczenie:
ABSTRACT Patient satisfaction reflects the quality of an institution’s delivery of health care services. Patient satisfaction is a critical factor in improvement or complete recuperation to wellness because satisfied patients will mean better compliance to treatment or follow up. As reported in the 2017 Annual OPD census of the Department of Obstetrics and Gynecology, there were 2617 total patient consultations. Majority of these (2138 or 81.7 %) were obstetrical cases. The average number of consultations per day (for Obstetrics and Gynecology patients combined) is 91. Therefore, the Out-Patient Clinic plays an important role in prenatal care specifically the prevention of adverse maternal and neonatal morbidity and mortality. This study aimed to assess the level of patient satisfaction among obstetrical patients in the Out Patient Department of the Obstetrics and Gynecology Section at Metropolitan Medical Center from July 1, 2018 to July 31, 2018 and to see the relationship between socio-demographic characteristic and the level of patient satisfaction. This is a descriptive, cross sectional study. The level of patient satisfaction assessed as to physical facilities, interaction between doctor and patient, interaction between nurses and patient, and registration service. There were sixty three subjects in this study. Sixty three were satisfied with inclusion criteria. The validated questionnaire was the pretested questionnaire which was 96 % valid and reliable by Cronbach’s analysis. Statistical analysis was done which showed respondents were generally satisfied. There were significant relationship association between socio-demographic characteristics and level of patient satisfaction with P value < 0.05.Key Word : Patient Satisfaction, Socio Demographic Characteristic
Style APA, Harvard, Vancouver, ISO itp.
7

Silva, Dulciléia Martins da, Carla Viana Dendasck i Euzébio de Oliveira. "The Social Worker’s Attendance to Cancer Patients". Revista Científica Multidisciplinar Núcleo do Conhecimento 05, nr 08 (26.11.2017): 39–51. http://dx.doi.org/10.32749/nucleodoconhecimento.com.br/health/patient-oncological.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
8

Sharma, Meenakshi. "Need to Adopt a Patient Centered Approach for Obtaining Favourable Results of NonPharmacological Interventions among Knee Osteoarthritis Patients in Out Patient Department Settings". International Journal of Healthcare Education & Medical Informatics 05, nr 02 (24.08.2018): 21–26. http://dx.doi.org/10.24321/2455.9199.201809.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
9

Album, Dag. "Patients' Knowledge and Patients' Work. Patient-Patient Interaction in General Hospitals". Acta Sociologica 32, nr 3 (lipiec 1989): 295–306. http://dx.doi.org/10.1177/000169938903200308.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
10

Cassels, Alan. "Patient speaking for patients". International Journal of Health Governance 21, nr 2 (6.06.2016): 89–95. http://dx.doi.org/10.1108/ijhg-02-2016-0014.

Pełny tekst źródła
Streszczenie:
Purpose – The purpose of this paper is to recognize the vital reasons for including public and patient voices in health policy decision-making, but illustrates the challenge it creates for decision-makers who must consider whether those voices represent patient interests or corporate interests. Design/methodology/approach – This paper takes the form of a narrative review. Findings – The history of flibanserin, a controversial new drug to treat a debatable condition, illustrates how a public relations campaign could circumvent the well-established process to weigh evidence of potential harm vs benefit by one of the most robust drug regulators in the world. Practical implications – It is both vital to recognize a fundamental problem that exists when corporate interests deceptively assume the mantle of “the patient voice” and then act to reduce that influence while supporting and building capacity in genuinely independent, consumer-focused activities. Originality/value – This paper suggests that organizations interested in consumer protection and the safe and cost-effective use of health resources create policies and procedures that can foster genuine consumer involvement while recognizing the danger to patient safety and consumer interests when consumer involvement is hijacked by vested interests.
Style APA, Harvard, Vancouver, ISO itp.
Więcej źródeł

Rozprawy doktorskie na temat "Patient"

1

O'Brien, Roxanne Louise. "Keeping patients safe: The relationship between patient safety climate and patient outcomes". Diss., Search in ProQuest Dissertations & Theses. UC Only, 2009. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:3378501.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
2

Söderholm, Werkö Sophie. "Patient Patients? : Achieving Patient Empowerment through active participation, increased knowledge and organisation". Doctoral thesis, Stockholms universitet, Företagsekonomiska institutionen, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-7261.

Pełny tekst źródła
Streszczenie:
This study examines patient empowerment in two local diabetes branch organisations in Sweden. In particular, the study focuses on the organisations’ membership, participation and influence on external actors. The overall aim of this thesis is to explore patient empowerment in order to discern what influence patient organisations and individual members can have and how they use it. This study is based on both quantitative and qualitative empirical data. Interviews with active members from two local diabetes organisations were conducted and a survey was carried out to identify the members’ thoughts and feelings about their membership, motivations, participation and influence, as well as to examine their local organisation, its work and influence. The findings form an overall picture of how members experience their organisation, memberships and empowerment. Characteristics of the two local patient branch organisations were identified and the leaders were found to be intensely dedicated people. The interviews, survey and participant observations revealed the members’ opinions about their organisation, their reasons for joining, their involvement, participation and influence, as well as their understanding of the local organisation and the Swedish Diabetic Association (SDA) and their possibility to empower them. Without organisations, members felt that they could not have a significant influence on external actors and events.
Style APA, Harvard, Vancouver, ISO itp.
3

Söderholm, Werkö Sophie. "Patient patients? : achieving patient empowerment through active participation, increased knowledge and organisation /". Stockholm : School of Business, Stockholm University, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-7261.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
4

Simard, Virginie. "Relations entre les comportements interpersonnels du psychothérapeute, la motivation des clients face à la thérapie et leur santé mentale /". Chicoutimi : Trois-Rivières : Université du Québec à Chicoutimi ; Université du Québec à Trois-Rivières, 2005. http://dx.doi.org/doi:10.1522/24604870.

Pełny tekst źródła
Streszczenie:
Thèse (M.Ps.) -- Université du Québec à Chicoutimi, 2005.
"Mémoire présenté à l'Université du Québec à Chicoutimi comme exigence partielle de la maîtrise en psychologie offerte à l'Université du Québec à Chicoutimi en vertu d'un protocole d'entente avec l'Université du Québec à Trois-Rivières." Comprend des réf. bibliogr. : f. [103]-115. Document électronique également accessible en format PDF.
Style APA, Harvard, Vancouver, ISO itp.
5

Klässbo, Maria. "HIP disability : patient education, classification and assessment /". Stockholm, 2003. http://diss.kib.ki.se/2003/91-7349-425-9/.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
6

Oi, Katsuya. "Understanding the Role of Patient Activation in the Association between Patient Socio-Economic Demographics and Patient Experience". PDXScholar, 2012. https://pdxscholar.library.pdx.edu/open_access_etds/467.

Pełny tekst źródła
Streszczenie:
This study focuses on the association between patient characteristics, which include both demographic and contextual factors, and patients' experiences with health care. The pre-existing literature provides rich information about patients' various demographics related to patient experience. Despite the abundance of empirical evidence showing that patients' demographics do affect how they perceive their health care. However, there is little to no empirical knowledge explaining the significance of such factors. As the existing literature points out the need for taking into contextual factors such as patient's beliefs, attitudes, skills that are pertinent to dealing with health care, my study proposes patient activation as such a contextual factor that explains the association between patient demographics and patient experience. Findings suggest that patient activation is a strong predictor of two patient experience measures: patients' rating of doctor-patient communication and their self-reported difficulties in getting needed care. However, it is also observed that the mediating effects of patient activation vary by the two dimensions of patient experiences. Though this study demonstrates that promoting patient activation may be able to normalize how patients report the quality of doctor-patient interaction, further research is needed to address access to care issues.
Style APA, Harvard, Vancouver, ISO itp.
7

Morrical, Kathy Jo S. "Readiness to learn as described by adults experiencing a change in health/illness status". Virtual Press, 2003. http://liblink.bsu.edu/uhtbin/catkey/1272425.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
8

Ramones, Valerie. "Patient education and compliance in the hypertensive elderly". Thesis, The University of Arizona, 1988. http://hdl.handle.net/10150/276814.

Pełny tekst źródła
Streszczenie:
This study examined the difference among 3 patient education intervention strategies and compliance in the hypertensive elderly. The strategies were verbal instructions, written instructions and both verbal and written instructions. An ex post facto descriptive design was implemented based on a Cognitive Information Processing Theory of Learning. Forty subjects were recruited and interviewed. Data analysis revealed that compliance did not differ significantly with the type of educational strategy.
Style APA, Harvard, Vancouver, ISO itp.
9

Pernet, Adeline. "Coproduire un soin sûr et efficace : le développement des capabilités des patients en radiothérapie". Thesis, Paris, CNAM, 2013. http://www.theses.fr/2013CNAM0906/document.

Pełny tekst źródła
Streszczenie:
Cette recherche traite de la participation des patients à la sécurité des soins en radiothérapie, qui se définit comme les actions mises en œuvre par les patients pour réduire la probabilité d’erreurs médicales et/ou pour atténuer les effets des erreurs lorsqu’elles surviennent effectivement. La sécurité des patients en radiothérapie est devenue une priorité centrale pour les politiques publiques suite aux accidents récents survenus à Épinal, Toulouse ou Grenoble pour les plus emblématiques. Dans ce contexte, la participation des patients peut être un moyen d'amélioration de la sécurité des soins. L’objectif général de cette étude est de comprendre la dynamique constructive des capabilités des patients dans la coproduction d’un soin sûr et efficace. Les capabilités des patients se définissent comme les contributions réelles faites par ces derniers et visant à assurer la sécurité et l'efficacité des soins.L'étude est menée dans les services de radiothérapie d’un hôpital et d'un centre de lutte contre le cancer. Plusieurs méthodes ont été combinées pour analyser l'activité de travail des manipulateurs, des patients et de l’activité conjointe entre ces deux partenaires : des observations des séances de traitement, des entretiens semi- directifs avec des manipulateurs et des patients, des auto- et allo -confrontations avec des manipulateurs et des entretiens d'explicitation avec des patients.Les résultats décrivent les contributions effectives mises en œuvre par les patients, et montrent que la coopération du patient agit comme une barrière de sécurité supplémentaire qui renforce la sécurité et l'efficacité du traitement. L'environnement et la durée de radiothérapie (traitement répétitif sur plusieurs semaines) sont des ressources externes qui fournissent une opportunité créative pour le patient d’apprendre de la situation et de l'évaluer en observant ce qui se passe. L'étude s’attache également à analyser les facteurs qui permettent (facteurs dits « positifs ») ou au contraire empêchent (facteurs dits « négatifs ») de convertir les capacités des patients en capabilités, c’est-à-dire en contributions effectives. Les facteurs de conversion positifs sont relatifs aux patients (connaissance des risques associés aux soins, motivation personnelle), au collectif manipulateur-patient (objectif commun, synchronisation cognitive, synchronisation opératoire) et aux manipulateurs (construction d’une relation de confiance, encouragement et renforcement positif). Cependant, les capabilités des patients ne sont pas toujours optimisées et les fortes pressions temporelles rencontrées par les manipulateurs dans leur pratique peuvent empêcher leur développement.Cette étude a permis de montrer qu’il y a une volonté conjointe des professionnels et des patients d’aller ensemble vers une meilleure coopération. Elle montre également que la coopération du patient est une nécessité qui reste encore méconnue et sous-exploitée, alors qu’elle permettrait probablement de réduire le nombre de situations et des comportements à risques des patients. Cette participation active, si elle ne doit en aucun cas être exigée et être une source d’anxiété supplémentaire pour le patient, mérite d’être développée et encouragée
This research deals with patient participation to patient safety, which can be defined as the actions taken by patients to reduce the likelihood of medical errors and / or mitigate the effects of errors when they do occur. Patient safety in radiotherapy has become a central priority for public policies further to the recent accidents arisen at Épinal, Toulouse and Grenoble for the most symbolic. In this context, patient participation may be a way of improvement of patient safety. The general objective of this study is to understand the constructive dynamics of patient capabilities in the co-production of a safe and effective care. Patient capabilities are defined as the actual contributions made by patients to ensure the safety and effective of care.The study was conducted in the radiotherapy departments of a public hospital and of a cancer center. Several methods have been combined to analyze the work activity of radiographers, of patients and of joint activity between the two partners : observations of treatment sessions, semi-structured interviews with manipulators and patients, self- and allo-confrontations with radiographers and elicitation interviews with patients.The results describe the actual contributions carried out by patients and show that patient cooperation acts as an additional safety barrier for patient safety. The environment of care and the duration of radiotherapy (repetitive and long treatment) constitute external resources, which provide a creative opportunity for the patient to learn from the situation and to evaluate it by observing what happens. The study also attempts to analyze the factors that allow ("positive" factors) or prevent ("negative" factors) patient capacities to become capabilities, i.e. actual contributions. The positive conversion factors are relative to the patients (knowledge of risks associated to care, personal motivation), to the collective (common objective, cognitive synchronization, operative synchronization) and to radiographers (construction of a trust relationship, encouragement and positive strengthening). However, patient capabilities are not always optimized and the strong work-related temporal pressures can prevent their development.This study highlights that there is a common will of professionals and patients to go together towards a better cooperation. It also shows that patient cooperation is a necessity that remains still unknown and underexploited, while it would likely reduce the number of risky situations and patients’ risky behaviors. Even if this active participation should not be required and be an additional source of anxiety for the patient, it should be developed and encouraged
Style APA, Harvard, Vancouver, ISO itp.
10

Kshetri, Kanak Bikram. "Modelling patient states in intensive care patients". Thesis, Massachusetts Institute of Technology, 2011. http://hdl.handle.net/1721.1/76985.

Pełny tekst źródła
Streszczenie:
Thesis (M. Eng.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, 2011.
Cataloged from PDF version of thesis.
Includes bibliographical references (p. 71-74).
Extensive bedside monitoring in hospital Intensive Care Units (ICU) has resulted in a deluge of information on patient physiology. Consequently, clinical decision makers have to reason with data that is simultaneously large and high-dimensional. Mechanisms to compress these datasets while retaining their salient features are in great need. Previous work in this area has focused exclusively on supervised models to predict specific hazardous outcomes like mortality. These models, while effective, are highly specific and do not generalize easily to other outcomes. This research describes the use of non-parametric unsupervised learning to discover abstract patient states that summarize a patient's physiology. The resulting model focuses on grouping physiologically similar patients instead of predicting particular outcomes. This type of cluster analysis has traditionally been done in small, low-dimensional, error-free datasets. Since our real-world clinical dataset affords none of these luxuries, we describe the engineering required to perform the analysis on a large, high-dimensional, sparse, noisy and mixed dataset. The discovered groups showed cohesiveness, isolation and correspondence to natural groupings. These groups were also tested for enrichment towards survival, Glasgow Coma Scale values and critical heart rate events. In each case, we found groups which were enriched and depleted towards those outcomes.
by Kanak Bikram Kshetri.
M.Eng.
Style APA, Harvard, Vancouver, ISO itp.
Więcej źródeł

Książki na temat "Patient"

1

Association of British Pharmaceutical Industry. i Long-Term Medical Conditions Alliance, red. Medicines & patients: Patient information. London: Association of the British Pharmaceutical Industry, 1997.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
2

Banks, Linda Jo. Patient care guidelines for tube feeding patients. Des Moines, Iowa: Briggs Corp., 1989.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
3

Sue, Bell, i National Cancer Alliance, red. ' Patient-centred cancer services'?: What patients say. Oxford: National Cancer Alliance, 1996.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
4

Alliance, National Cancer, red. "Patient-centred cancer services"?: What patients say. Oxford: National Cancer Alliance, 1996.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
5

Alliance, National Cancer, red. "Patient-centred cancer services"?: What patients say. Oxford: National Cancer Alliance, 1996.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
6

Roberts, Helen. The patient patients: Women and their doctors. London: Pandora Press, 1985.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
7

Alliance, National Cancer, red. " Patient-centred cancer services"?: What patients say. Oxford: National Cancer Alliance, 1996.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
8

Shua, Ana María. Patient. Pittsburgh, PA: Latin American Literary Review Press, 1997.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
9

Vincent, Karen. Is there a link between patient perception and patient compliance in injured sports patients? Northampon: Nene College, 1993.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
10

L, Shortridge Dennis, i Watson Phyllis M. 1947-, red. Patients first: Experiences of a patient-focused pioneer. Chicago, Ill: Health Administration Press, 1996.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
Więcej źródeł

Części książek na temat "Patient"

1

Sheridan, Susan, Heather Sherman, Allison Kooijman, Evangelina Vazquez, Katrine Kirk, Nagwa Metwally i Flavia Cardinali. "Patients for Patient Safety". W Textbook of Patient Safety and Clinical Risk Management, 67–79. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-59403-9_6.

Pełny tekst źródła
Streszczenie:
AbstractUnsafe care results in over 2 million deaths per year and is considered one of the world’s leading causes of death. In 2019, the 72nd World Health Assembly issued a call to action, The Global Action on Patient Safety, that called for Member States to democratize healthcare by engaging with the very users of the healthcare system—patients, families, and community members—along with other partners—in the “co-production” of safer healthcare.The WHO’s Patients for Patient Safety (PFPS) Programme, guided by the London Declaration, addresses this global concern by advancing co-production efforts that demonstrate the powerful and important role that civil society, patients, families, and communities play in building harm reduction strategies that result in safer care in developing and developed countries. The real-world examples from the PFPS Programme and Member States illustrate how civil society as well as patients, families, and communities who have experienced harm from unsafe care have harnessed their wisdom and courageously partnered with passionate and forward-thinking leaders in healthcare including clinicians, researchers, policy makers, medical educators, and quality improvement experts to co-produce sustainable patient safety initiatives. Although each example is different in scope, structure, and purpose and engage different stakeholders at different levels, each highlights the necessary building blocks to transform our healthcare systems into learning environments through co-production of patient safety initiatives, and each responds to the call made in the London Declaration, the WHO PFPS Programme, and the World Health Assembly to place patients, families, communities, and civil society at the center of efforts to improve patient safety.
Style APA, Harvard, Vancouver, ISO itp.
2

Friedman, Mildred. "Patient to Patient". W Diabetic Nephropathy, 213–21. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4613-2287-0_13.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
3

Beleffi, Elena, Paola Mosconi i Susan Sheridan. "The Patient Journey". W Textbook of Patient Safety and Clinical Risk Management, 117–27. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-59403-9_10.

Pełny tekst źródła
Streszczenie:
AbstractThe wide implementation of patient safety improvement efforts continues to face many barriers including insufficient involvement of all stakeholders in healthcare, lack of individual and organizational learning when medical errors occur and scarce investments in patient safety. The promotion of systems-based approaches offers methods and tools to improve the safety of care. A multidisciplinary perspective must include the involvement of patients and citizens as fundamental contributors to the design, implementation, and delivery of health services.The patient journey is a challenging example of using a systems approach. The inclusion of the patient’s viewpoint and experience about their health journey throughout the time of care and across all the care settings represents a key factor in improving patient safety. Patient engagement ensures that the design of healthcare services are aligned with the values, the preferences, and needs of the patient community and integrates the real-life experience and the skills of the people to enhance patient safety in the patient journey.The utmost priority to implement patient engagement is the training of patients. Therefore, training for both patients/families/advocates and health professionals is the foundation on which to build active engagement of patients and consequently an effective and efficient patient journey.The chapter offers examples of successful training courses designed to foster strategic alliances among healthcare professionals and researchers with patients and their organizations. Training of patients constitutes the first step to develop shared knowledge, co-produced projects, and the achievement of active multilevel participation of patients for the implementation of patient safety in the patient journey.
Style APA, Harvard, Vancouver, ISO itp.
4

von Kummer, Rüdiger, Luigi Bozzao, Claude Manelfe, S. Bastianello i H. Zeumer. "Patient Scans: Patients 1–20". W Early CT Diagnosis of Hemispheric Brain Infarction, 7–87. Berlin, Heidelberg: Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-642-79893-1_3.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
5

Citerio, G., C. Giussani, Hugo Sax, Didier Pittet, Xiaoyan Wen, John A. Kellum, Angela M. Mills i in. "Immunocompromised Patient = Immunosuppressed Patient". W Encyclopedia of Intensive Care Medicine, 1206. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-00418-6_1739.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
6

Nahler, Gerhard. "patient". W Dictionary of Pharmaceutical Medicine, 131. Vienna: Springer Vienna, 2009. http://dx.doi.org/10.1007/978-3-211-89836-9_1007.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
7

D’Angelosante, Melania. "Patient". W Dictionary of Statuses within EU Law, 409–18. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-00554-2_52.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
8

Hughes, Dea M. "Patient Identification". W Patient Safety, 3–18. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-7419-7_1.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
9

Montgomery, Christopher, i Eric Wei. "Patient Identification". W Patient Safety, 75–87. Cham: Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-35933-0_6.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
10

Andersen, Bjørg Marit. "Patient Protection Is Patient Safety". W Prevention and Control of Infections in Hospitals, 3–12. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-99921-0_1.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.

Streszczenia konferencji na temat "Patient"

1

Barinov, Evgeny, Nadezhda Dobrovolskaya, Anastasia Ivanova, Ruslan Kalinin, Alexander Manin, Natalya Mikheeva i Pavel Romodanovsky. "Patient dissatisfaction with medical dental care". W Issues of determining the severity of harm caused to human health as a result of the impact of a biological factor. ru: Publishing Center RIOR, 2020. http://dx.doi.org/10.29039/conferencearticle_5fdcb03a353ad3.76128786.

Pełny tekst źródła
Streszczenie:
The article provides information on the results of studying the materials of 150 commission of forensic medical examinations on the facts of patient dissatisfaction with the provision of medical care. The relevance of the problem of the legal relationship between a doctor and a patient is revealed and shown. The lack of information on these issues leads to a high probability of disputed situations in the providing dental care, so there is an urgent need for an integrated approach to the implementation of legally defined rights of patients. Media coverage of the above-mentioned problems plays an important role in improving the level of legal competence of patients. At the same time, the direct relationship between the doctor and the patient is the most important mechanism for implementing the patient's rights at the dental appointment and preventing conflicts. Behavior of doctors in such cases should be strictly regulated by normative legal acts. The process of information sharing with patients and transfer of information to the patient's relatives should receive in medical preventive institution specific legal basis under sections 30, 31, 48, 61 “Principles of legislation of the Russian Federation about health protection of citizens”, to be fixed in job descriptions with the designation of responsibility.
Style APA, Harvard, Vancouver, ISO itp.
2

Otani, Kagari, i Yasunobu Ito. "Acquisition and sharing of knowledge and skills of visiting nurses in Japan". W 13th International Conference on Applied Human Factors and Ergonomics (AHFE 2022). AHFE International, 2022. http://dx.doi.org/10.54941/ahfe1002554.

Pełny tekst źródła
Streszczenie:
The purpose of this study is to clarify, through ethnographic research, how nurses acquire and share their knowledge and skills of home nursing in clinical settings. The field research took place at a visiting nurse station in Nagoya, Japan between 2013 and November 2021. Research method used were participant observations and interviews at visiting nurse station and patients’ homes. One of the authors is an assistant professor of nursing at a university’s Nurse and Health department who also leads students in the clinical training at the visiting nurse station. The research data were acquired from periodical nurse station visits and from accompanying nurses in their activities.visiting nurses considered patients and family as partners, and they explored the preferred care together with the patient to create tailored care. We showed the following in a paper at AHFE-HSSE conference in 2021: the visiting nurses read into the patient’s societal background, life and beliefs, and visiting nurses analyzed the living style patients wish for, in order to propose the method which materialize this kind of living. The value co-created by the nurses and patient formulated the “normal living style” wished to be sustained by the patient (Otani and Ito 2021).Incidentally, in nursing education in Japan, universities nursing faculties and nursing schools educate students in basic knowledge and skills of nursing in wards to home nursing in Japan. The co-creative practices and techniques of visiting nursing care need to be learned while working in a clinical setting after the nurse is licensed. The paper revealed the following: The visiting nurse "co-created" with the patient to produce a nursing technique that fit the patient's needs based on the "sticky information" (von Hippel 1994) obtained in the patient's home. At the visiting nurse station, the nurses reported new information obtained at the patient's home or communicated to the patient during daily conferences. The nurse illustrated and demonstrated the nursing techniques that fit the patient to colleague nurses.In addition, the nurses had a joint conference with physical, occupational, and speech therapists working in the same station. The participants reported to each other the new information the patient during their stay at the patient's home, and described the techniques of each specialist that fit the patients. The information revealed in the conference was recorded into the patient's medical chart each time. The nursing skills created in the patient's home through co-creation with the patient are sticky information that is difficult to transfer, but they are shared and accumulated through gestural demonstrations at conferences by the health professionals.
Style APA, Harvard, Vancouver, ISO itp.
3

Kim, Jonghyeok, Hosung Kwon, Jonghyeon Kim, Jinsoo Park, Soong-Un Choi i Sookyung Kim. "PillGood: Automated and Interactive Pill Dispenser Using Facial Recognition for Safe and Personalized Medication". W Thirty-First International Joint Conference on Artificial Intelligence {IJCAI-22}. California: International Joint Conferences on Artificial Intelligence Organization, 2022. http://dx.doi.org/10.24963/ijcai.2022/854.

Pełny tekst źródła
Streszczenie:
Safety of taking medicine prescribed differently to each patient in hospital relies on the discernment of medical professionals who deals with measuring pill quantity, packaging, and distributing. It is difficult and time consuming to keep track of medication record of each patient. Also, medication safety is prone to be in risk due to the human error. To help patients get accurate medication following their prescription plan with minimizing human labors and mistakes, we developed PillGood, an automated smart pill dispenser system using facial recognition technique. PillGood provides real-time and personalized guidance to take the correct medicine by alarming patients and distributing exact quantity of pills at specific time following each patient's prescription table. The system notify patients through mobile app and speaker when they need to take the medicine, and detect who the patient is through the machine learning based face recognition. Then, based on each patient's prescribing information, the controller distributes pills to each patient. Results show that PillGood enable highly accurate personalized pill dispensation followed by precise face recognition, benefiting both patients and medical professionals. Videos for demonstrating the system can be found on https://youtu.be/Wx7bXxRGjXA
Style APA, Harvard, Vancouver, ISO itp.
4

Morris, Nichole, Curtis Craig, Katelyn Schwieters, Bradley Drahos, Marshall Mabry, Eugene Floersch i William Kessler. "Limited training in undergarment and clothing removal techniques to expose wounds in combat care". W AHFE 2023 Hawaii Edition. AHFE International, 2023. http://dx.doi.org/10.54941/ahfe1004367.

Pełny tekst źródła
Streszczenie:
A critical component of combat casualty care is to fully expose the patient to identify and treat injuries. Completing these actions under stressful conditions is expected to require adequate training. In this study 21 combat lifesaver trained soldiers were surveyed regarding their recent training exposing chest injuries of male and female soldiers. Nearly all participants (95.2%) reported experience in treating male simulated patients; however, only 52.4% reported any experience applying a chest seal on a male human or simulated patient and only 28.6% reported any experience removing the t-shirt of a male human or simulated patient. Seven participants (33.3%) reported experience in treating female simulated patients, 23.8% reported at least some experience applying a chest seal to a female human or simulated patient, and only 9.5% reported experience removing the female patient’s t-shirt and, similarly, a female patient’s bra. Findings suggest a pronounced gap in the CLS training curriculum.
Style APA, Harvard, Vancouver, ISO itp.
5

McGregor, J. L., L. McGregor, M. Hans, A. Sayegh, M. C. Trzeeiak i M. Dechavanne. "PLATELETS OF A PATIENT LACKING GLYCOPROTEINS lib AND Ilia AGGREGATE TO HIGH CONCENTRATIONS OF THROMBIN OR COLLAGEN". W XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643863.

Pełny tekst źródła
Streszczenie:
The aim of this study was to investigate the platelets of a patient having bleeding episodes that began in infancy. The patient’s platelets in citrated-PRP did not aggregate when stimulated with ADP (5 and 10 uM), collagen (2.5 ug/ml), or sodium arachidonate (1 uM). However, washed patient platelets, in the presence of 2mM calcium, aggregated and secreted when stimulated with high concentrations of thrombin (0.36, 0.72 and lU/ml) or collagen (2, 4, 10 ug/ml). Monoclonal antibodies (Mab) LYP18 (directed against the IIb-IIIa glycoprotein complex) and LYP8 (anti-thrombospondin) inhibited thrombin and collagen induced aggregation of control but not the patient platelets. Patient thrombin -stimulated platelets did not bind 125I-labelled fibrinogen (40 to 320 ug/ml). Moreover, stimulating the washed patient's platelets with ADP (10-100 uM), in the presence of fibrinogen (2mg/ml), did not result in aggregation. Binding studies using Mab 125I-LYP2 (directed against the IIb-IIIa glycoprotein complex) showed the absence of the complex on the patient's platelets. The absence of the IIb-IIIa complex on the patient's platelets was also observed using crossed immunoelectro -phoresis and Mab 125I-LYP2 or 125I-LYP18. Individual glycoproteins (lib or Ilia) were not detected on silver stained two-dimensional (non-reduced/reduced) SDS-PAGE. Moreover, Western blots of |he patients platelets used in combination with anti-PLA or anti-LEK polyclonal antibodies failed to detect the presence of these two glycoproteins. These results indicate that this patient has Glanzmann's thrombasthenia or a variant of this disease. Moreover, this study shows that platelets lacking the IIb-IIIa glycoprotein complex can aggregate in responseto collagen or thrombin in the presence of physiological concentrations of calcium.
Style APA, Harvard, Vancouver, ISO itp.
6

Chu, Sauman, Allyson Hart i Marilyn Bruin. "A patient-centered approach in designing a kidney transplant decision aid". W AHFE 2023 Hawaii Edition. AHFE International, 2023. http://dx.doi.org/10.54941/ahfe1004234.

Pełny tekst źródła
Streszczenie:
The kidney transplant decision aid tool (https://www.srtr.org/tools/kidney-transplant-decision-aid/) was designed, created, and included as part of the Scientific Registry of Transplant Recipients (SRTR) resource website. The decision aid tool was created with input from patients with kidney disease and the doctors who care for them. An extensive information gathering and testing process with user-centered approach was implemented. Ten interviews and 4 focus group discussion sessions were held with an average of 4.5 patients in each group to gather preliminary design and content directions. Two additional focus groups with a total of 12 kidney transplant providers and 4 additional national focus group discussions with a total of 19 patients were held afterward to discuss the created content and design approach. Finally, 15 individual patient testing sessions were conducted to refine the content, design, and navigation of the tool. The tool is intended to be used during patient’s visit with their doctor as the patient learns about kidney transplant. Our goal is to provide informative materials to empower patients by helping them understand treatment options and outcomes. The doctor will guide patient through the tool and explain the information to help them to make informed decisions.The decision aid tool contains concise information to compare the pros and cons of dialysis vs. transplant treatments, living donor vs. deceased donor transplant, accepting higher quality vs. lower quality deceased donor kidney offers, and increased infectious risk kidneys vs. standard infectious risk kidneys. We also created a calculator to estimate a patient’s likely outcomes on the kidney transplant wait list based on the transplant regions or center and the individual’s medical condition. Preliminary testing suggests that patients find the tool and the likely outcomes helpful in leading to informative decision making.
Style APA, Harvard, Vancouver, ISO itp.
7

Ciliberti, Rosella, Alessandro Bonsignore, Liliana Lorettu, Maurizio Secchi, Michele Minuto, Pierluigi Santi i Ilaria Baldelli. "Physician/patient relationship following hospital discharge – new methods of therapeutic and care continuity". W the 8th International Workshop on Innovative Simulation for Healthcare. CAL-TEK srl, 2019. http://dx.doi.org/10.46354/i3m.2019.iwish.013.

Pełny tekst źródła
Streszczenie:
"Healthcare organization aims to shorten hospitalization times, both to facilitate patient turnover and to avoid the risks of the nosocomial environment. Between March and September 2018, patients that were discharged after hospitalization for scheduled reconstructive breast surgery were given a portable device with the Dr. Link app installed, created to allow real-time communication with physicians. Patients and physicians completed a satisfaction survey on their experience with the use of the device. Analysis shows overall patient satisfaction in terms of improvement in relationships and quality of life. Physicians reported more responsible patient behaviour, better compliance, and earlier treatment of complications. Continuous interactive assistance can improve the discharged patient’s quality of life and therapeutic path. However, the device risks becoming a negative tool if the health care professional has not made the proper initial emotional investment in the relationship, delegating the totality of the therapeutic relationship to the tablet."
Style APA, Harvard, Vancouver, ISO itp.
8

Arunachalam, Priya, i Brendan D’Souza. "Patient-Centered Hospital Gowns: A Novel Redesign of Inpatient Attire to Improve Both the Patient and Provider Experience". W 2022 Design of Medical Devices Conference. American Society of Mechanical Engineers, 2022. http://dx.doi.org/10.1115/dmd2022-1058.

Pełny tekst źródła
Streszczenie:
Abstract During their inpatient stays, patients are often required – or highly encouraged – to wear hospital gowns. While these gowns are intended to be convenient for patients and their providers, their design has remained largely unchanged over time. As healthcare moves towards greater emphasis on patient-centered care, the hospital gown is an opportunity to improve patient care. Patients have expressed frustration with the traditional hospital gown, especially with how revealing the gown can be. Here, we introduce a redesigned hospital gown that addresses many common concerns related to patients’ comfort and privacy. Our design introduces novel midline, rear, and shoulder panels, which provide healthcare workers with convenient access to the patient while maintaining coverage over areas of the patient that are not being examined. These panels also make it less likely for patients to be inappropriately exposed during routine activities. A prototyped gown was developed to test design features, and evaluation of this prototype demonstrated that this novel design has the potential to address many concerns while protecting the usability of traditional gowns. Further improvements to the gown’s design are also discussed.
Style APA, Harvard, Vancouver, ISO itp.
9

Gothard, Andrew T., i Steven R. Anton. "A Method to Generate 3D Patient-Specific Total Knee Arthroplasty Tibia Models". W ASME 2022 Conference on Smart Materials, Adaptive Structures and Intelligent Systems. American Society of Mechanical Engineers, 2022. http://dx.doi.org/10.1115/smasis2022-91008.

Pełny tekst źródła
Streszczenie:
Abstract Geometric information about a patient’s anatomy is vital in pre-operative planning for orthopedic surgeries. At present, many physicians rely on the analysis of 2D scans, such as radiographs, magnetic resonance images (MRIs), or computed tomography (CT) scans, in order to visualize a patient’s geometry. Research is being done to develop patient-specific 3D bone geometry to aid in pre-operative planning and assist in creating personalized finite element models that can help predict complications or failure after surgery. While 3D models are incredibly useful and have been developed for several parts of the human anatomy, there is still a great need for cost-effective ways to create personalized total knee arthroplasty (TKA) models. Currently, methods for creating patient-specific knee geometries typically only consider patients without TKA implants, rely on expensive medical imaging, such as layered CT scans, or require a large database of 3D models. This work presents a novel semi-automated process to create patient-specific 3D tibia geometry for TKA patients using pairs of standard, low-cost bi-planar radiographs. The method presented involves two main stages. In the first stage, the geometric bone contours from each view of the tibia are extracted from two bi-planar radiographs using gradient thresholding and Canny edge detection on user-defined regions of interest. The second stage aligns the two extracted tibia contours with a generic 3D tibia model from the 6th SimTK Grand Challenge Dataset and then modifies the generic 3D model to match the radiographic contours using a full-ellipse scaling and shifting (FESS) method. The effectiveness of the FESS method is evaluated by comparing the contours of the generated patient-specific model in the anteroposterior (AP) and lateral views to the radiograph contours in the AP and lateral views using difference calculations for three TKA patients. The maximum difference between the patient-specific models and the radiographs in both AP and lateral views is found to be on the order of 1 mm.
Style APA, Harvard, Vancouver, ISO itp.
10

Manno, Francis A. M., Sinai H. C. Manno, Irfan Ahmed, Yuanchao Liu, Shuk Han Cheng i Condon Lau. "One Patient, Two Patient, Three Patient, Four - When Patients Are Counted, But Not Accounted For: Pseudoreplication In Medicine". W 2018 9th International Conference on Information Technology in Medicine and Education (ITME). IEEE, 2018. http://dx.doi.org/10.1109/itme.2018.00065.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.

Raporty organizacyjne na temat "Patient"

1

DiBenedetti, Dana B., T. Michelle Brown, Carla Romano, Claire Ervin, Sandy Lewis i Sheri Fehnel. Conducting Patient Interviews Within a Clinical Trial Setting. RTI Press, sierpień 2018. http://dx.doi.org/10.3768/rtipress.2018.op.0054.1808.

Pełny tekst źródła
Streszczenie:
Qualitative data centered on patients’ experiences and perspectives typically go uncollected in clinical trial settings. Yet patients’ treatment experiences offer complementary insights and context on topics such as disease management, treatment gaps, and previous treatments outside of those gathered in traditional patient-reported outcome questionnaires. Qualitative interviews can capture patients’ perceptions of treatment needs, more fully explore meaningful changes experienced as a result of treatment, and reveal outcomes that are most important to patients. Asking patients detailed questions can provide insight into the “why” of a patient’s expressed thought or feeling. The inclusion of patient interviews within clinical trials is a relatively new and evolving field of research. This article delineates the types of data that may be collected during interviews with clinical trial participants and outlines two approaches to conducting qualitative research in the clinical trial setting, with a focus on maximizing the value of the resulting data.
Style APA, Harvard, Vancouver, ISO itp.
2

Dolfini-Reed, Michelle, i Derek Shia. Patient Access Study. Fort Belvoir, VA: Defense Technical Information Center, marzec 1998. http://dx.doi.org/10.21236/ada346941.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
3

Oi, Katsuya. Understanding the Role of Patient Activation in the Association between Patient Socio-Economic Demographics and Patient Experience. Portland State University Library, styczeń 2000. http://dx.doi.org/10.15760/etd.467.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
4

Ryland, Howard, i Sarah Bunn. Reforming the Mental Health Act - Approaches to Improve Patient Choice. Parliamentary Office of Science and Technology, UK Parliament, maj 2023. http://dx.doi.org/10.58248/pn695.

Pełny tekst źródła
Streszczenie:
The Mental Health Act 1983 has been criticised as being overly restrictive, with inadequate scope for patient choice and autonomy. The Government’s Draft Mental Health Bill proposes reforms to improve patient choice. A joint parliamentary committee report on the draft Bill recommended further changes to enhance choice, including a statutory duty to offer patients advance choice documents. Reports to date suggest that advance care planning could offer some benefits, but uptake can be low. Proposals to replace the Nearest Relative who has certain powers under the Act, with a Nominated Person of the patient’s choosing, have been widely welcomed. There are questions about operationalisation and safeguarding. Alongside the reforms, the Government is piloting ‘culturally appropriate advocacy’, which preliminary findings suggest could help advocates better support patients from ethnic minority backgrounds. The draft Bill removes learning disabilities and autism as grounds for detention under Section 3 of the Act. Stakeholders have raised concerns about unintended diversion to more restrictive pathways, such as the criminal justice system. A range of stakeholders share the view that careful implementation is needed to maximise the benefits of proposed reforms. The Government has not announced when the Bill will be introduced.
Style APA, Harvard, Vancouver, ISO itp.
5

Mertz, Lynn. Reducing Health Disparities in Patients with a High Patient Adversity Index. Washington, DC: AARP Thought Leadership, czerwiec 2024. http://dx.doi.org/10.26419/int.00056.030.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
6

Yuan, Bo, Wei Cao, Xieyu Zhang, Yue Yang i Jiahe Zhao. Telemedicine effect on rheumatoid arthritis : A protocol for a systematic review and meta-analysis of randomized controlled trials. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, styczeń 2022. http://dx.doi.org/10.37766/inplasy2022.1.0109.

Pełny tekst źródła
Streszczenie:
Review question / Objective: The role of telemedicine has been highlighted by researchers in many fields as a potential advantage for improving quality of life, increasing patient adherence, and alleviating patient concerns. Telemedicine is patient-acceptable with high satisfaction rates in patients with rheumatoid arthritis (RA). However, there is a lack of consistent results among important indicators regarding RA, such as patient pain assessment and health-related quality of life. Thus, we plan to perform a systematic review and meta-analysis to assess the effect of telemedicine on patients with RA. Information sources: PubMed, Embase, and Cochrane Library databases.
Style APA, Harvard, Vancouver, ISO itp.
7

Sauer, Michael C. Patient Satisfaction and Productivity. Fort Belvoir, VA: Defense Technical Information Center, maj 2008. http://dx.doi.org/10.21236/ada493869.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
8

DEPARTMENT OF THE ARMY WASHINGTON DC. Medical Services: Patient Administration. Fort Belvoir, VA: Defense Technical Information Center, marzec 2001. http://dx.doi.org/10.21236/ada403180.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
9

Herman, Clifford M. Trauma Patient Followup Registry. Fort Belvoir, VA: Defense Technical Information Center, lipiec 1987. http://dx.doi.org/10.21236/ada206650.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
10

Sinanan, Mika N. Patient Safety Center Organization. Fort Belvoir, VA: Defense Technical Information Center, czerwiec 2006. http://dx.doi.org/10.21236/ada469244.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
Możesz być także zainteresowany rozszerzonymi bibliografiami na temat „Patient” dla poszczególnych typów źródeł:
Artykuły w czasopismach Rozprawy doktorskie Książki
Oferujemy zniżki na wszystkie plany premium dla autorów, których prace zostały uwzględnione w tematycznych zestawieniach literatury. Skontaktuj się z nami, aby uzyskać unikalny kod promocyjny!

Do bibliografii