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1.
Clin Ter ; 175(3): 176-180, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38767075

RESUMO

Abstract: Organ donation after euthanasia (ODE) is a complex procedure involving the patient, the family, and the medical staff. Most organ donations occur from patients declared brain dead, and healthcare professionals rely on surrogate decisions, or the possible expression of ante-mortem will. Organ donation from deceased individuals is thus feasible under rigorous conditions, while direct donation after euthana-sia is not possible. The scientific community has not reached a shared conclusion. It is also difficult to quantify the number of patients who would be medically eligible to donate organs after euthanasia. In keep-ing with the core the principle of self-determination, any decision to undergo euthanasia (with or without organ donation) must be voluntary and not influenced by external pressures. For this reason, the physician should avoid informing the patient about the possibility of donating their organs before their request for euthanasia is evaluated. Just as noteworthy is the issue of healthcare providers' conscientious objec-tion and the receiving patient's right to know whether the transplanted organs come from a subject who underwent euthanasia. Finally, the patient who requests to end their life does so primarily because they are tormented by unbearable suffering and often expresses, as a last wish, the desire to exercise their free will regarding their own body. Organ donation after euthanasia would therefore seem to reinforce patient autonomy and self-esteem, thus giving a different meaning to their inevitable death, which is useful in saving the lives of others.


Assuntos
Obtenção de Tecidos e Órgãos , Humanos , Eutanásia/psicologia , Autonomia Pessoal , Morte Encefálica
2.
Eur Rev Med Pharmacol Sci ; 26(2): 643-652, 2022 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-35113440

RESUMO

The article aims to elaborate on European policy choices for the prevention of SARS­CoV­2 contagion, with a close focus on the rules and regulations enacted in Italy so far. European states have ruled out generalized vaccination mandates but have so far preferred to exert a form of "moral suasion", through the introduction of a digital certificate which can only be granted to those who are vaccinated, cured of COVID-19 or tested negative through an antigen test in the previous 48 hours. Italy has applied this tool, dubbed "Green Pass", very rigorously: many daily activities, including going to work, are only allowed for those who have the certificate. A one-year Green Pass is issued after vaccination, although data show that vaccine protection may subside gradually over about six months; the cost of the antigen tests every 48 hours is to be borne by the patient. Testing the unvaccinated is essential to contain the spread of the infection, but it would have been more logical to mandate that all the unvaccinated undergo regular testing (for example every ten days), instead of imposing a test every 48 hours only to be allowed to engage in some activities. The authors stress that in order to minimize the risk of future possible pandemics, prevention strategies are needed, and poor countries need to be enabled to vaccinate their populations in order to prevent new variants from developing. The pledges made by world leaders in that regard during the recent G20 summit must therefore be honored, for the sake of global health that never in our lifetime has been so threatened.


Assuntos
Vacinas contra COVID-19/administração & dosagem , COVID-19/prevenção & controle , Política Pública , Vacinação/psicologia , COVID-19/epidemiologia , COVID-19/virologia , Teste Sorológico para COVID-19 , Vacinas contra COVID-19/imunologia , Humanos , Consentimento Livre e Esclarecido , Itália/epidemiologia , Pandemias , SARS-CoV-2/isolamento & purificação , Recusa do Paciente ao Tratamento
3.
Eur Rev Med Pharmacol Sci ; 25(22): 6874-6880, 2021 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-34859849

RESUMO

Scientific and technological advances in the diagnosis of neoplastic disease and the introduction of increasingly accurate and personalized anti-cancer treatments have significantly improved the chances of survival of most cancer patients, particularly at a young age. Since the interest of the research community in the life prospects of young cancer survivors has been growing, a new branch of medicine has emerged in recent years that reconciles the potentially gonadotoxic treatments of cancer with the preservation of fertility: oncofertility. The possibility of preserving one's fertility can be of great benefit for the psychological well-being of cancer patients, whose mental health is already severely tested by the cancer diagnosis. Although national and international guidelines urge doctors to start early a discussion on fertility conservation issues (reproductive counseling), still little is known as to the awareness of oncofertility by young cancer survivors and the information they receive about it.


Assuntos
Sobreviventes de Câncer , Aconselhamento , Preservação da Fertilidade , Fertilidade , Humanos , Neoplasias/terapia
4.
Eur Rev Med Pharmacol Sci ; 25(23): 7354-7362, 2021 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-34919235

RESUMO

The article aims to elaborate the progress made in partial ectogenesis research on sheep as well as human embryos. Since the ban on embryos experimentation after the 14-day window is a major roadblock in terms of partial ectogenesis research, the authors have weighed the possibility that such a ban could be reconsidered. In favor of easing such a restriction, it may be argued that: (a) unlike the Catholic approach, prevalent ethics precepts hold that the embryo's interest ought to be balanced against the interests of the other parties involved; (b) an extension of the 14-day deadline would no longer make ethically untenable practices acceptable; hence, the "slippery slope" argument, although generally worthy, would not conclusively apply to partial ectogenesis; (c) in mainstream embryo research efforts, there is a conflict between the lives of embryos and the health of individuals already born; as for partial ectogenesis, however, such a conflict would be between the lives of embryos and the lives of fetuses which would not survive otherwise. Still, in light of the embryo's status as a human being, the authors conclude that such research practices should only be allowed on supernumerary embryos.


Assuntos
Ectogênese/ética , Pesquisas com Embriões/ética , Útero , Animais , Embrião de Mamíferos/fisiologia , Feminino , Feto , Humanos , Ovinos , Fatores de Tempo
5.
Clin Ter ; 172(3): 197-205, 2021 May 05.
Artigo em Inglês | MEDLINE | ID: mdl-33956036

RESUMO

BACKGROUND: Over the process of establishing the causal relation-ship, medical and legal methodologies may be at variance over the definitional standards and terminologies applied, which can hinder the activities of expert witnesses. OBJECTIVES: The article's authors have set out to assess whether, and under what conditions, a causal relationship can be established between acoustic neuroma and exposure to non-ionizing radiation from mobile communication devices. METHODS: The study design is a Systematic Review. The authors have drawn upon a 2020 Turin Court of Appeals ruling which found such a causal relationship in a somewhat peculiar case: rare tumor and exposure to non-ionizing radiation of unusually long and regular dura-tion. The case presents several peculiarities, herein analyzed in light of a) scientific evidence relative to the etiopathogenesis of the neuroma; b) available medico-legal literature defining causality evaluation criteria, and lastly c) court filings in regard to the probability standards applied to prove causal relationship. RESULTS: A direct tie cannot be proven, not even in cases of sub-stantially intense and lengthy exposure, if the medico-legal standards applied are not consistent enough to prove that nexus is more likely than not. DISCUSSION: Several elements suggest a causal relationship is unlikely: a) a dearth of evidence on humans; b) rats exposed to such radiation have developed cardiac tumors, not in their ears; c) exposure has caused no tumors in mice; d) the length of exposure is incompat-ible with tumor size and type. That fourth point only concerns the case herein explored, whereas the first three have a general scope of validity. The main limitation of the present study design is the heterogeneity among the included studies. Retrospective and prospective studies have been included, which may be a source of bias.


Assuntos
Computadores de Mão , Neuroma Acústico/etiologia , Exposição Ocupacional/efeitos adversos , Animais , Causalidade , Humanos , Camundongos , Radiação não Ionizante/efeitos adversos , Ratos , Fatores de Risco
6.
Eur Rev Med Pharmacol Sci ; 25(5): 2449-2456, 2021 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-33755984

RESUMO

Countries responded to the COVID-19 pandemic with various levels of restrictions and lockdown in an effort to save lives and prevent the saturation and collapse of national health systems. Unfortunately, the blockades have entailed hefty socioeconomic costs. In order to contrast the spread of the virus, states have used contact tracing technology, in the form of mobile phone applications designed to track close contacts of those infected with COVID-19. Recent research has shown the effectiveness of this solution, particularly when used in conjunction with manual tracking. Nonetheless, the contact tracing app raises concerns due to the potential privacy implications. The authors have delved into the European legislation that protects privacy through the principles of proportionality and minimization, arguing that in order to quickly resolve the pandemic caused by COVID-19, one cannot blindly trust the exclusive help of technology. Instead, we need the involvement of health personnel, scientists, and no less importantly, the citizenry's sense of solidarity and the duty to abide by the rules of social distancing, the use of protective devices and hygiene rules to protect public health.


Assuntos
Busca de Comunicante/métodos , Infecções por Coronavirus/prevenção & controle , COVID-19/epidemiologia , Telefone Celular , Confidencialidade , Infecções por Coronavirus/epidemiologia , Humanos , Aplicativos Móveis , Pandemias/prevenção & controle , Distanciamento Físico , Privacidade , SARS-CoV-2 , Tecnologia
7.
Eur Rev Med Pharmacol Sci ; 25(3): 1752-1761, 2021 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-33629345

RESUMO

The CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats)/Cas9 (CRISPR-associated protein 9) system enables scientists to edit diverse genome types with relative ease, with the aim - in the near future - to prevent future human beings from developing genetic diseases. The new opportunities arising from the system are broad-ranging and revolutionary, but such prospects have also been the cause for alarm throughout the international scientific community. The authors have laid out a review of the trials carried out so far in terms of genome editing, for the ultimate purpose of weighing implications and criticisms. We feel that possible valuable alternatives, such as induced pluripotent stem cells should not be overlooked.


Assuntos
COVID-19 , Proteínas Associadas a CRISPR/genética , Sistemas CRISPR-Cas , Repetições Palindrômicas Curtas Agrupadas e Regularmente Espaçadas , SARS-CoV-2/isolamento & purificação , COVID-19/terapia , COVID-19/virologia , Proteína 9 Associada à CRISPR/genética , Edição de Genes , Terapia Genética , Humanos , SARS-CoV-2/genética
10.
Acta Otorhinolaryngol Ital ; 38(3): 273-276, 2018 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-29984805

RESUMO

SUMMARY: In current healthcare, delivery of medical and surgical treatment takes place in a multidisciplinary manner. This raises the problem of distinguishing the conditions under which the person who has properly carried out his duties, respecting the related leges artis, can be held responsible for damages materially caused by another member of the medical team. Jurisprudence has developed the so-called "principle of trust" for which every member of the team can rely on the fact that other members are acting in compliance with the leges artis of their specialisation. The Supreme Court has limited the application of this principle. The authors examine the jurisprudence on responsibility of the team in otolaryngology and conclude that individual liability should be limited to the specific expertise of the individual specialist.


Assuntos
Responsabilidade Legal , Erros Médicos/legislação & jurisprudência , Otolaringologia/legislação & jurisprudência , Equipe de Assistência ao Paciente/legislação & jurisprudência , Humanos
12.
Int J Law Psychiatry ; 56: 58-64, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29701600

RESUMO

The authors aim to analyze the key aspects related to the testimony of children who might have been victims of sexual harassment and abuse. The issue of medico-legal psychiatric assessment of minors who claim to have been sexually abused is extremely contentious and widely-debated, not only due to the growing spread of such claims, but also on account of the technical challenges it raises. For these reasons, national as well as European lawmakers have intervened by enacting new legislation, and scientific communities have established new sets of guidelines aimed at improving the overall conditions under which a child is called to testify as well as the process through which depositions are collected and evaluated, so as to ensure that any assessment of the reliability of the testimony is scientifically grounded. The authors also highlight the importance of regulatory measures meant to minimize the risk that the questioning of a child might negatively affect his or her emotional balance by limiting and lessening stressful conditions and anxiety, which may traumatize and irretrievably scar the child. Moreover, they stress the importance of dealing with the social issue of child abuse by strengthening a preventive set of measures.


Assuntos
Abuso Sexual na Infância , Vítimas de Crime/psicologia , Competência Mental , Adolescente , Humanos , Itália , Aplicação da Lei , Incerteza
13.
Eur Rev Med Pharmacol Sci ; 22(4): 1161-1167, 2018 02.
Artigo em Inglês | MEDLINE | ID: mdl-29509270

RESUMO

This review illustrates some brief considerations of the medical use of cannabis recently issued in Italy. History and uses of cannabis throughout centuries and different countries are illustrated together with a description of botany and active phytocannabinoids. Then, medical use of cannabis anti-pain treatment for patients resistant to conventional therapies is described in case of chronic neuropathic pain, spasticity, for anticinetosic and antiemetic effect in nausea and vomiting caused by chemotherapy, for appetite stimulating effect in cachexia, anorexia, loss of appetite in cancer patients or patients with AIDS and in anorexia nervosa, hypotensive effect in glaucoma resistant to conventional therapies and for reduction of involuntary body and facial movements in Gilles de la Tourette syndrome. Italian most recent legislation on medical cannabis is detailed with some law proposals, also showing the inconsistent legislation within European Union. Some final considerations of future studies are also reported.


Assuntos
Legislação de Medicamentos/tendências , Maconha Medicinal/uso terapêutico , Manejo da Dor/tendências , Antieméticos/uso terapêutico , Caquexia/tratamento farmacológico , Caquexia/epidemiologia , Europa (Continente)/epidemiologia , Humanos , Itália/epidemiologia , Espasticidade Muscular/tratamento farmacológico , Espasticidade Muscular/epidemiologia , Náusea/tratamento farmacológico , Náusea/epidemiologia , Neoplasias/tratamento farmacológico , Neoplasias/epidemiologia , Neuralgia/tratamento farmacológico , Neuralgia/epidemiologia , Manejo da Dor/métodos , Síndrome de Tourette/tratamento farmacológico , Vômito/tratamento farmacológico , Vômito/epidemiologia
14.
Clin Ter ; 169(2): e82-e85, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29595871

RESUMO

The paper's authors aim to elaborate on the innovations brought by law n. 24/2017, issued by the Italian Parliament with a close focus on art. 5, which pertains to the drafting of guidelines and the adoption of best practices. The guidelines constitute in fact an element of innovation brought by the above-mentioned law, and compliance with them can shield from possible liability those health care professionals who find themselves embroiled in professional accidents while in the fulfillment of their duties. Besides, there are several critical aspects within the law that need to be highlighted as well. As far as best practices are concerned, the lawmakers who drafted the legislation make no mention as to the standards of evidence needed in order to characterize any given professional behavior as "best practice". The reform appears unlikely to be effective in providing doctors with clear behavioral standards, thus reducing the margin for liability claims against them.


Assuntos
Atenção à Saúde/legislação & jurisprudência , Atenção à Saúde/normas , Erros Médicos/legislação & jurisprudência , Guias de Prática Clínica como Assunto/normas , Humanos , Itália , Responsabilidade Legal
15.
Eur Rev Med Pharmacol Sci ; 21(22): 5290-5296, 2017 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-29228447

RESUMO

Uterus transplantation was firstly tested with animal trials sixty-five years ago. Despite several successful attempts in human subjects, the different procedures still lay at the experimental stage, in need of further studies and investigations before they can be considered as standard clinical practices. Uterus transplant cannot be regarded as a life-saving procedure, but rather a method to restore woman ability to procreate, when lost, thus improving her quality of life. Uterus transplant is a complex surgical procedure and presents significant health threats. Medical staff should therefore always obtain informed consent from patients, emphasizing such risks. Before that, women undergoing uterine transplants should be thoroughly informed about the hazards inherent to the procedure and especially about the dangers of immunosuppressant drugs, administered after the surgery which may injure the fetus, eventually formed in the restored organ and even lead to its death, thus nullifying the purpose of the transplant itself. Therefore, the risk-benefit ratio of uterus transplantation needs to be carefully assessed and described.


Assuntos
Infertilidade Feminina/cirurgia , Transplante de Órgãos/ética , Transplante de Órgãos/legislação & jurisprudência , Doenças Uterinas/cirurgia , Útero/transplante , Adulto , Feminino , Humanos , Medição de Risco
16.
Clin Ter ; 168(3): e214-e219, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28612900

RESUMO

Law no. 41/2016, enacted after a parliamentary debate characterized by a strong media pressure, intends to give a strong response to the growing social alarm caused by road accidents causing deaths. In this perspective, it introduced the categories of road homicide and road injuries within the Penal Code and the new hypotheses of mandatory and facultative arrest in flagrante delicto. This paper aims at comparing the rules by which the United Kingdom, France, Spain, Germany and Italy protect people's lives and safety of vehicular traffic in order to highlight strengths and weaknesses with a view to future reforms. A survey on the European legislature highlights that, while other countries tend to criminally sanction several dangerous driving conducts, Italy has preferred, on the one hand, to punish only with administrative sanctions some violations related to reckless driving (with the exception of driving under the influence of alcohol and drugs) and, on the other, to provide for particularly harsh prison sentences in the case of vehicular homicide. The authors criticize this approach and other aspects of the new law. Moreover, it seems that the legislator's aim has not been achieved because traffic accidents have not decreased. They also believe that better results could be obtained by increasing controls on the roads and developing a policy of economical investments which improves road safety.


Assuntos
Acidentes de Trânsito , Condução de Veículo/legislação & jurisprudência , Homicídio , Acidentes de Trânsito/legislação & jurisprudência , Etanol , França , Alemanha , Humanos , Itália , Reino Unido
17.
Clin Ter ; 168(3): e220-e224, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28612901

RESUMO

Amniotic fluid embolism (AFE) is a pregnancy complication known to be extremely hard to diagnose, since it manifests itself abruptly and with no warning signs, presenting an incidence rate of about 1 in 40000 deliveries, and maternal morbidity and mortality ranging from 20% to 60%. Although almost a century has gone by since it was first identified (1926) and despite medical research having been conducted on such a syndrome, diagnostic procedures and treatment methods have not yet been clarified enough. Specific biochemical markers have been produced in research laboratories, but their clinical value results to be limited, given how rapid the pathological process moves forward. At the time being, no diagnosis is feasible which may effectively prevent the disease from occurring. Certainly, a multidisciplinary approach might contribute to saving the lives of mother and infant, as well as ensuring better life standards. The paper's authors aim to highlight the medico-legal issues, in light of several rulings from the Italian Constitutional Court as well as lower courts. The authors also advocate for the creation of a nation-wide registry meant to collect all signaled AFE instances so that research on this as yet devastating syndrome can be conducted based on hard data.


Assuntos
Embolia Amniótica , Imperícia/legislação & jurisprudência , Adulto , Embolia Amniótica/mortalidade , Feminino , Humanos , Itália , Gravidez , Fatores de Risco
18.
Clin Ter ; 168(2): e128-e132, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28383624

RESUMO

The authors analyze from an ethical and legal point of view the case of a 37 year old man, hospitalized for four days because of a 'dissociative syndrome', who had introduced in both his orbits a portable radio antenna. Most likely, he completed the self-enuclation using his own hands. He was brought to the Ophtalmic Hospital by nurses who handed the two eyeballs to the physicians who ascertained that the corneas were intact. Then, they performed the conservative extraction. In the following days those corneas were transplanted (keratoplasty) on two subjects on the waiting list at that hospital. The case raises the question of whether it is lawful and ethically acceptable to take, for transplant use, the corneas of a mentally incapable patient who has excised his own eyeballs. The authors analyze the case from the angle of the Italian law and Oviedo Convention. Neither of them has a specific regulation on this topic. It is therefore necessary to apply general principles that holdvalidfor Italy and a variety of countries worldwide. Particularly, the choice to use the corneas for transplant did not prejudice the physical integrity of the patient, who could no longer utilize his own eyeballs. His self-determination has not been affected; in fact, he was not in the position to make a conscious decision. Additionally, the so-called "implied consent" could be applied. Therefore, the principle of human solidarity, which is the moral duty to benefit others, seems to prevail in the case at hand.


Assuntos
Transplante de Córnea/legislação & jurisprudência , Consentimento Livre e Esclarecido , Autonomia Pessoal , Adulto , Transplante de Córnea/métodos , Humanos , Itália , Masculino
19.
Clin Ter ; 168(2): e113-e119, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28383622

RESUMO

The authors discuss the emergency contraception (EC) topic, assessing scientific and ethical aspects. The almost totality of the studies carried out tends to report on the use of drugs as an emergency measure to prevent pregnancy. However, it is not yet completely excluded that emergency contraceptives can induce medical abortion. The debate on side effects of EC continues to be a highly emotional and controversial issue both for advocates who believe they will lower considerably the number of unintended pregnancies and abortions, and for opponents who believe that using emergency contraception amounts to an abortion. This latter hypothesis highlights the conflicting aspect of the conscientious objection to abortion of physicians and pharmacists. This research work is aimed at investigating the emergency contraception issue, paying particular attention to the medico-legal and regulatory aspects of this subject. Particularly, the authors focus on the conscientious objection in order to assess, if any, legal protection for physicians and pharmacists who claim a right to conscientious objection. Inappropriate use of EC could be resolved through a registry of user. This registry, of course, would not have the intention of persecution, but would only serve to detect possible cases of subjugation, exploitation and harassment.


Assuntos
Anticoncepção Pós-Coito/psicologia , Médicos/psicologia , Recusa em Tratar , Consciência , Feminino , Humanos , Gravidez
20.
Eur Rev Med Pharmacol Sci ; 20(22): 4628-4634, 2016 11.
Artigo em Inglês | MEDLINE | ID: mdl-27906442

RESUMO

In recent years there has been an exponential increase of fillers use in aesthetic medicine. The popularity of this anti-wrinkle product is based on their capacity to offer significant improvement in the aesthetic field, particularly to skin rejuvenating processes with non-invasive and less expensive techniques, if compared to the surgical methods (i.e. surgical lifting). The great number of fillers on the market is composed of a large heterogenic number of biomaterials. The aim of this review was to provide an overview and a classification of the filling materials that are most commonly used. A synthesis of the literature concerning fillers and related side effects was also reported. The law decree no. 23 of 1998, converted in the law no. 94 of 1998 and the principal judgments of the Italian Court of Cassation have been examined with the medico-legal issues related to fillers use in medicine. With respect to their degradation, filler materials may be classified as temporary (degradable), semi-permanent and permanent (not degradable). The temporary fillers such as hyaluronic acid and collagen are completely degraded by the surrounding tissue in a few months. The permanent fillers, such as the ones derived from silicon oil and minerals are not biodegradable and may cause serious and irreversible side effects. Their use requires a physician with a high level of specialization to perform the treatment, a deep knowledge of face anatomy and a great degree of experience.


Assuntos
Estética , Envelhecimento da Pele , Materiais Biocompatíveis , Colágeno , Técnicas Cosméticas , Humanos , Ácido Hialurônico
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