Wszystkie pola: patient's consent - Katalog OPAC zbiorów

Skocz do pozycji: 1.

Tytuł:: Prawo pacjenta - dziecka do wyrażenia zgody na udzielenie świadczenia zdrowotnego
The right of a child - patient to give a consent for a healthcare service
Autorzy:: Wołoszyn - Cichocka, Agnieszka
Powiązania:: https://bibliotekanauki.pl/articles/1046857.pdf
Data publikacji:: 2018-12-09
Wydawca:: Katolicki Uniwersytet Lubelski Jana Pawła II
Tematy:: świadoma zgoda
małoletni pacjent
świadczenie zdrowotne
informed consent
minor patient
healthcare service
Opis:: Prawo do wyrażenia zgody na udzielenie świadczenia zdrowotnego jest jednym z najistotniejszych praw pacjenta, jednakże w stosunku do dzieci, jest ono ograniczone. Zasadą jest, że pacjent małoletni, który ukończył 16 lat wyraża zgodę na działanie medyczne razem ze swoim przedstawicielem ustawowym, natomiast za pacjenta, który nie ukończył 16 lat, decyduje wyłącznie przedstawiciel ustawowy. Dla niektórych świadczeń zdrowotnych polski ustawodawca wprowadził jednak odmienne reguły. W sposób odmienny uregulował zasady wyrażania zgody przez pacjenta małoletniego na udział w eksperymencie medycznym, na pobranie komórek, tkanek i narządów w celu ich przeszczepienia, na pobranie krwi czy też na badanie psychiatryczne. Nadmierna kazuistyka przepisów w zakresie zgody pacjenta małoletniego na udzielenie świadczenia zdrowotnego niewątpliwie utrudnia ich poznanie i stosowanie.
A right to give a consent for a healthcare service is one of the most critical patients’ rights, but yet in relation to children it is limited. The principle is that the minor patient who turned 16 agrees for medical activities together with it’s legally designated representative; whereas for a patient who did not turn 16 decides exclusively the representative itself. For certain medical services Polish legislator introduced other rules. Differently regulated are rules concerning giving a consent by minor patients for participation in a medical experiment, for collection of the cells, tissues and organs for the purpose of transplantation, for taking blood or for a psychiatric examination. Excessive casuistry in accordance with the consent of a minor patient for a healthcare service undoubtedly make it’s understanding and applying more difficult.
Źródło:: Studia Prawnicze KUL; 2018, 4; 119-136
1897-7146
2719-4264
Pojawia się w:: Studia Prawnicze KUL
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 2.

Tytuł:: Por el consentimiento informado: el derecho a la información
Autorzy:: Fernández, David Aguilera
Borges de Meneses, Ramiro Délio
Powiązania:: https://bibliotekanauki.pl/articles/2130854.pdf
Data publikacji:: 2019
Wydawca:: Instytut Studiów Międzynarodowych i Edukacji Humanum
Tematy:: Clinical information
informed consent
patient
and law
Opis:: Objective: To know how the relationship between the clinic n and the patient is in providing the in- formation that concerns the health of the user, taking into account the Right of Information. Design: Bibliographic review. Materials and Methods: The search included publications that it did not exceed then years of age and whose complete text was found, focusing on systematic reviews. The search for updated systematic reviews in the chosen field of study through: The Cochrane Library Plus, Pubmed Health, Metabuscadores such as Trip, Bibliographic databases such as CUIDEN PubMed and other sources such as Google academic and magazines. The selected studies were previously submitted to a critical reading skills program (CASPe), whose scores were higher than seven. Fundamental Results: Information is a process, it is about dialogue, this information and obtaining informed consent can vary among patients, it is easy and fast in some cases and in others it may take time. The clinician sho- uld provide time for the patient to assimilate the information and express the doubts and questions that arise. Therefore, the clinician should strive during the dialogue, communicating and informing, to shape and see the limits of the process and clarify the consent of the patient. Conclusions: It is a commit- ment to Bioethics, on the part of all the clinicians involved in health care, to assume the commitment of philosophical reflection on all those ethical dilemmas that arise in daily practice. Communication should be a basic tool for the relationship between the clinician and the patient, and then used in moral deliberation. The clinician should encourage continuous exploration of his pa- tient without giving anything for granted, identify the concerns that the patient may be experiencing, encourage the empathic attitude, act from the congruence and provide the creation of a therapeutic link.
Źródło:: Humanum. Międzynarodowe Studia Społeczno-Humanistyczne; 2019, 1 (32); 105-115
1898-8431
Pojawia się w:: Humanum. Międzynarodowe Studia Społeczno-Humanistyczne
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 3.

Tytuł:: Evaluation of patient feedback following laparoscopic cholecystectomy based on information described in the informed consent form developed by the Association of Polish Sur
Autorzy:: Misiak, Piotr
Jabłoński, Sławomir
Lazarek, Jerry
Malinowska, Katarzyna
Santorek-Strumiłło, Edyta
Terlecki, Artur
Powiązania:: https://bibliotekanauki.pl/articles/1394302.pdf
Data publikacji:: 2015
Wydawca:: Index Copernicus International
Tematy:: laparoscopic cholecystectomy
informed consent
Opis:: The cholecystectomy procedure is the most routinely performed intervention in general surgery. The current international gold standard is via the laparoscopic approach. It is a safe, minimally-invasive procedure; however, it is associated with complications in 1% of cases. The aim of the study was to analyze patient feedback, by means of a survey, to determine how much knowledge patients possessed about their disease state and proposed surgical intervention, based primarily on information contained within the informed consent form developed by the Association of Polish Surgeons. Material and methods. This study involved the participation of 51 patients who underwent laparoscopic cholecystectomy, indicated by a diagnosis of gallstones, in the years 2014 and 2015. Results. Despite having signed the informed consent form, there was considerable variation among the responses given to the survey by the 51 patients in this study. Some patients’ responses were tangential to the questions asked; many patients did not respond to any of the sub points. Conclusions. Given that this study is based on a small sample size of patients, it must be presumed that the process by which the patient declares his or her informed consent requires further consideration with respect to the means by which it is obtained. The authors of this study thus recommend that multimedia resources be harnessed as part of the process of obtaining the informed consent of patients prior to surgical intervention.
Źródło:: Polish Journal of Surgery; 2015, 87, 11; 558-564
0032-373X
2299-2847
Pojawia się w:: Polish Journal of Surgery
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 4.

Tytuł:: Biological Medicinal Therapy in terms of Respecting Patients’ Rights – Assessment of the Present Legal Status in Poland
Autorzy:: Zimmermann, Agnieszka E.
Susłowska, Natalia
Powiązania:: https://bibliotekanauki.pl/articles/895517.pdf
Data publikacji:: 2020-04-29
Wydawca:: Polskie Towarzystwo Farmaceutyczne
Tematy:: patient safety
patients’ rights
biological medicinal product
informed consent
Opis:: Introduction: Patients’ rights must be respected at every stage of therapy, including during biological drug therapy. For clinicians, it is key to be involved in the decision-making process with regard to the choices of medication and possible drug substitution. In Poland, the law encourages automatic drug substitution and does not recognise disparities in biological drugs. Aim: The main aim of the paper is to describe the present legal situation depicting the scope of autonomy of a hospitalised patient. Methods: An analysis was conducted of the Polish regulations, the doctrine and administrative decisions and European Medicines Agency guidance documents. Results: In Poland, patients who require therapy with advanced technologies such as biopharmaceuticals, may obtain access to a medicine within a special drug reimbursement programme in a hospital. Hospitals are supplied with the drugs necessary for drug therapy programmes via public procurement. This means that hospital procurement procedures decide which drug a patient will receive. It is not the decision of the health care provider. In view of this, the Polish Patient Ombudsman, in a decision confirmed by the Provincial Administrative Courts, pointed out that the selection of a drug for therapy should depend on current medical knowledge rather than on the result of a tender carried out by a hospital. Conclusions: Polish solutions based on the lack of an obligatory requirement to consult a substitution with a treating physician deviate from the standard practices followed in numerous EU countries and the US.
Źródło:: Acta Poloniae Pharmaceutica - Drug Research; 2020, 77, 2; 373-379
0001-6837
2353-5288
Pojawia się w:: Acta Poloniae Pharmaceutica - Drug Research
Dostawca treści:: Biblioteka Nauki

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