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2.
Pediatr Blood Cancer ; 62(9): 1609-15, 2015 Sep.
Article in English | MEDLINE | ID: mdl-25925227

ABSTRACT

BACKGROUND: In El Salvador, about 200 new cases of pediatric cancer are diagnosed each year, and survival rates approach 70%. Although treatment is available at no cost, abandonment of therapy has remained at a steady yearly rate of 13% during the past decade. A time sensitive adherence tracking procedure (TS-ATP) was recently implemented to detect missed appointments, identify their causes, and intervene promptly. Procedure The study team was informed daily of patient/family failure to attend medical appointments in the pediatric oncology unit; the families were contacted and interviewed to ascertain and address the reasons. Patients who did not return after this initial contact were contacted again through local health clinics and municipalities. Law enforcement was a last resort for patients undergoing frontline treatment with a good prognosis., The system was adapted to clinical urgency: families of patients undergoing induction therapy were contacted within 24 hr, those in other therapy phases, within 48 hr, and those who had completed treatment, within one week. Reasons for absence were obtained by telephone or in person. RESULTS: The annual rate of abandonment was reduced from 13-3% during the 2 years period. There were 1,111 absences reported and 1,472 contacts with caregivers and institutions. The three main reasons for absences were financial needs (165, 23%), unforeseen barriers (116, 16%), and domestic needs (86, 12%). CONCLUSIONS: Use of the treatment adherence tracking system to locate and communicate with patients/families after missed appointments and the allocated aid stemming from these interviews substantially reduced abandonment and non-adherence.


Subject(s)
Neoplasms/psychology , Patient Dropouts/psychology , Treatment Refusal/psychology , Adolescent , Cancer Care Facilities/organization & administration , Caregivers/psychology , Child , Child, Preschool , El Salvador/epidemiology , Electronic Health Records , Female , Hospitals, Pediatric/organization & administration , Humans , Infant , Law Enforcement , Male , Motivation , Neoplasms/epidemiology , Neoplasms/therapy , Oncology Service, Hospital/organization & administration , Patient Compliance , Patient Dropouts/legislation & jurisprudence , Patient Dropouts/statistics & numerical data , Patient Education as Topic , Persuasive Communication , Poverty , Professional-Family Relations , Social Work Department, Hospital/organization & administration , Telephone , Tertiary Care Centers/organization & administration , Time Factors , Treatment Refusal/legislation & jurisprudence , Treatment Refusal/statistics & numerical data
4.
Health Aff (Millwood) ; 33(5): 848-55, 2014 May.
Article in English | MEDLINE | ID: mdl-24799583

ABSTRACT

In 1978 the federal government restricted research on prison and jail inmates in medical studies, the result of decades of unethical research in correctional institutions. We evaluated the impact this policy has had on studies of health outcomes in minority populations, particularly studies involving black men, who are disproportionately incarcerated. Specifically, we explored the effect of incarceration on follow-up rates of fourteen prospective clinical studies funded by the National Heart, Lung, and Blood Institute. We estimated that during the past three decades high rates of incarceration of black men may have accounted for up to 65 percent of the loss to follow-up among black men in these studies. The impact of incarceration was far less among white men, black women, and white women. These estimates suggest that the ability of those studies to examine racial disparities in health outcomes, as well as to understand the experience of this group, could be compromised. We believe that community-recruited subjects who are incarcerated should be allowed to continue participating in observational clinical research that poses minimal risk to participants.


Subject(s)
Black People/statistics & numerical data , Clinical Trials as Topic/statistics & numerical data , Healthcare Disparities/statistics & numerical data , Patient Dropouts/statistics & numerical data , Prisoners/statistics & numerical data , Adolescent , Adult , Aged , Bias , Clinical Trials as Topic/ethics , Clinical Trials as Topic/legislation & jurisprudence , Cohort Studies , Ethics, Research , Follow-Up Studies , Healthcare Disparities/ethics , Healthcare Disparities/legislation & jurisprudence , Humans , Male , Middle Aged , National Heart, Lung, and Blood Institute (U.S.) , Patient Dropouts/legislation & jurisprudence , Patient Selection/ethics , Prisoners/legislation & jurisprudence , Prospective Studies , United States , Young Adult
6.
Int J Drug Policy ; 24(6): e25-34, 2013 Nov.
Article in English | MEDLINE | ID: mdl-23623719

ABSTRACT

BACKGROUND: The behavior of police is an important factor in drug users' access to preventive and therapeutic health services. In China, opiate users must be registered and approved by police before accessing methadone maintenance treatment (MMT). METHODS: We conducted a literature review to identify studies reporting original data about the influence of Chinese drug policing activities on MMT access and outcomes. Searches were conducted in PubMed, the Law Journal Library of HeinOnline, the Social Science Citation Index and China Academic Journals of CNKI for empirical studies conducted in China and published in academic journals between 2005 and April 2012. RESULTS: The initial literature search retrieved 276 records, of which 85 were included in the review and 191 were excluded. The majority of the included papers were single-clinic observational studies. These studies reported that: (1) fear of incarceration deterred users from initiating and continuing MMT; (2) the rates of MMT referral by police were considerably lower than those by drug user peers and by community and the media; (3) police sending users to compulsory detoxification (DETOX) and reeducation through labor (RTL) centers contributed to higher rates of MMT patient dropout; (4) arrests in and around MMT clinics were not uncommon; (5) cooperation between local police and public health agencies was difficult to achieve; and (6) a limited number of trial programs were conducted to refer detainees in DETOX to MMT clinics after release, but the outcomes were not promising. CONCLUSION: Reviewed studies report drug policing practices that appear to be impeding MMT access and reducing successful treatment outcomes. Research focusing on the nature, prevalence and severity of these effects is urgently needed. Health and public security officials in China should review and reform policies and practices of registering, monitoring, and incarcerating drug users.


Subject(s)
Analgesics, Opioid/therapeutic use , Drug Users/legislation & jurisprudence , Drug and Narcotic Control/legislation & jurisprudence , Health Policy/legislation & jurisprudence , Health Services Accessibility/legislation & jurisprudence , Methadone/therapeutic use , Opiate Substitution Treatment , Opioid-Related Disorders/drug therapy , Police/legislation & jurisprudence , Professional Role , China , Cooperative Behavior , Crime/legislation & jurisprudence , Drug Users/psychology , Fear , Humans , Interdisciplinary Communication , Opioid-Related Disorders/diagnosis , Opioid-Related Disorders/psychology , Patient Dropouts/legislation & jurisprudence , Prisons/legislation & jurisprudence , Referral and Consultation , Treatment Outcome
7.
Nervenarzt ; 84(1): 65-71, 2013 Jan.
Article in German | MEDLINE | ID: mdl-22215222

ABSTRACT

With its verdict in May 2011 the German Federal Constitutional Court declared the current law for preventive detention unconstitutional and obliged the legislative bodies to undertake a freedom- and treatment-oriented reform. Psychiatrists and psychotherapists are bound to provide therapeutic concepts. Currently there is a lack of information on the intended clientele. In our study we examined 26 persons serving preventive detention, 32 regular prisoners and 29 non-delinquent probands. The groups were matched according to age and intelligence. We gathered sociodemographic data, criminal records and conducted the tests SCID I, SCID II und PCL-R, K-FAF and BIS-11 to obtain diagnoses and characteristics. Based on this information, the HCR-20 and GAF were performed. In comparison to regular prisoners and non-delinquents, the group of those serving preventive detention is characterised by medium to advanced age, antisociality, psychopathy, substance abuse or addiction, aggressivity, a strong criminal record, years of imprisonment, insufficient educational and vocational training and a high risk of recidivism. In our examination of persons serving preventive detention, we demonstrate that this clientele is a group of recidivists difficult to treat. The current laws and a lack of early intervention programs have prevented and delayed their timely and possibly successful treatment. From a psychiatric point of view, there is a strong need for new therapeutic concepts to meet this challenge.


Subject(s)
Commitment of Mentally Ill/legislation & jurisprudence , Commitment of Mentally Ill/statistics & numerical data , Crime/prevention & control , Crime/statistics & numerical data , Dangerous Behavior , Deinstitutionalization/legislation & jurisprudence , Mental Disorders/rehabilitation , Patient Compliance/psychology , Patient Compliance/statistics & numerical data , Prisoners/legislation & jurisprudence , Prisoners/psychology , Security Measures/legislation & jurisprudence , Security Measures/statistics & numerical data , Adult , Age Factors , Aged , Aggression/psychology , Antisocial Personality Disorder/diagnosis , Antisocial Personality Disorder/epidemiology , Antisocial Personality Disorder/psychology , Comorbidity , Crime/psychology , Cross-Sectional Studies , Health Care Reform/legislation & jurisprudence , Humans , Male , Mental Disorders/diagnosis , Mental Disorders/epidemiology , Mental Disorders/psychology , Middle Aged , Patient Advocacy/legislation & jurisprudence , Patient Dropouts/legislation & jurisprudence , Patient Dropouts/psychology , Patient Dropouts/statistics & numerical data , Patient Readmission/legislation & jurisprudence , Patient Readmission/statistics & numerical data , Prognosis , Risk Factors , Secondary Prevention , Socioeconomic Factors , Substance-Related Disorders/diagnosis , Substance-Related Disorders/epidemiology , Substance-Related Disorders/psychology , Substance-Related Disorders/rehabilitation , Switzerland , Treatment Outcome
9.
Int J Offender Ther Comp Criminol ; 56(4): 539-56, 2012 Jun.
Article in English | MEDLINE | ID: mdl-21518702

ABSTRACT

To explore the effectiveness of court-supervised drug treatment for California parolees, offender characteristics, treatment experiences, and outcomes were examined and contrasted to those of probationers. The analysis used statewide administrative data on 4,507 parolees and 22,701 probationers referred to treatment by Proposition 36 during fiscal year 2006-2007. Compared with probationers, parolee problems were more severe at treatment entry, more were treated in residential settings, treatment retention was shorter, and fewer completed treatment. Regarding outcomes, fewer parolees were successful at treatment discharge and more recidivated over 12-months post admission. Both groups improved in many areas by treatment discharge, but improvements were generally smaller among parolees. Significant interaction effects indicated that parolees benefited from residential care and more treatment days, even after controlling for covariates. Court-supervised drug treatment for parolees can "work;" however, parolees have more frequent and diverse needs, and their outcomes are enhanced by more intensive treatment. Findings suggest methods for optimizing the effectiveness of criminal-justice-supervised programs for treating drug-dependent offenders.


Subject(s)
Prisoners/legislation & jurisprudence , Prisoners/psychology , Referral and Consultation/legislation & jurisprudence , Substance-Related Disorders/rehabilitation , Adult , California , Female , Humans , Male , Middle Aged , Patient Dropouts/legislation & jurisprudence , Patient Dropouts/psychology , Rehabilitation Centers/legislation & jurisprudence , Secondary Prevention , Substance-Related Disorders/prevention & control , Substance-Related Disorders/psychology , Treatment Outcome
10.
Int J Offender Ther Comp Criminol ; 56(1): 96-112, 2012 Feb.
Article in English | MEDLINE | ID: mdl-21187299

ABSTRACT

Nonattendance for and late cancellations of scheduled appointments, that is no-show, is a well-known phenomenon in psychiatric outpatient clinics. Research on the topic of no-show for initial and consecutive appointments in the field of forensic psychiatry is scarce. This study therefore aims to determine the prevalence and causes of no-show and to explore reasons for nonattendance. The study was carried out in an outpatient clinic in northern Netherlands. Telephone interviews were administered to 27 no-show clients, 84 follow-up no-show clients, and 41 attendees of 18 years and older. A no-show rate of 24.9% and a follow-up no-show rate of 9.8% was found. The majority of appointments missed were in the beginning phase of clinic contact. No-show clients were younger than their attending counterparts and more often dropped out from clinic contact. Also, less family social support was experienced by nonattendees. Reasons for nonattendance were having forgotten about appointment and work commitments.


Subject(s)
Ambulatory Care Facilities , Antisocial Personality Disorder/rehabilitation , Appointments and Schedules , Forensic Psychiatry , Mental Disorders/rehabilitation , Motivation , Patient Compliance/psychology , Patient Dropouts/psychology , Adult , Ambulatory Care/legislation & jurisprudence , Ambulatory Care/statistics & numerical data , Ambulatory Care Facilities/statistics & numerical data , Antisocial Personality Disorder/epidemiology , Antisocial Personality Disorder/psychology , Commitment of Mentally Ill/legislation & jurisprudence , Cross-Sectional Studies , Female , Follow-Up Studies , Forensic Psychiatry/legislation & jurisprudence , Forensic Psychiatry/statistics & numerical data , Humans , Male , Mental Disorders/epidemiology , Mental Disorders/psychology , Netherlands , Patient Compliance/statistics & numerical data , Patient Dropouts/legislation & jurisprudence , Patient Dropouts/statistics & numerical data , Risk Factors , Secondary Prevention , Social Support
12.
Rev. Méd. Clín. Condes ; 22(3): 397-403, mayo 2011.
Article in Spanish | LILACS | ID: lil-600339

ABSTRACT

El enfrentamiento de pacientes que rechazan la transfusión de hemoderivados, principalmente por motivos religiosos, continúa siendo un problema no resuelto. En el análisis de este conflicto convergen los conceptos de la bioética, destacando el respeto por la autonomía del paciente por un lado y la beneficencia, al cual estamos acostumbrados los médicos, por otro, lo que lleva a la enfrentamiento natural que se produce al tratar de prevalecer un concepto sobre el otro. El consentimiento informado constituye un elemento fundamental en el enfoque adecuado de este tema, pues nos permite desarrollar una mejor medicina en nuestras instituciones, manteniendo el respeto por el deseo del paciente. Existen numerosos ejemplos a nivel nacional e internacional, que sientan jurisprudencia en el caso de los pacientes Testigos de Jehová, los cuales debemos considerar, ya que la tendencia de los tribunales es respetar la voluntad de los pacientes más aun tratándose de decisiones autónomas y que no afectan al resto de la sociedad. El desarrollo institucional de programas terapéuticos, particularmente en la esfera quirúrgica, sin transfusión de hemoderivados, es una buena línea de desarrollo hacia una mejor calidad de Medicina Transfusional, respetando la autonomía de los pacientes.


Transfusion refusal of hemocomponents and/or hemoderivatives has become increasingly an important challenge in clinical settings, difficult to deal with. This procedure involves several bioethical and moral conflicts. Among them, the patient`s wish not to be transfused, the right to self-determination, the risk of a fatal outcome and, on the other hand, medical concerns, legal issues involved,the good clinical practice and the duty to attempt a cure. These considerations are not always easy to solve. Issues such as the latter one explain why Informed Consent (IC) is a crucial tool that allows a rational use of transfusional therapies and a better implementation of “blood-saving” techniques. Many clinical cases (mainly Jehovah`s witnesses patients) have set the basis of international jurisprudence. The current tendency is to respect the patient`s will, especially adults that have been fully advised of the consequences of not receiving tranfusional therapy.


Subject(s)
Humans , Bioethics , Informed Consent/ethics , Informed Consent/legislation & jurisprudence , Jehovah's Witnesses , Treatment Refusal/ethics , Treatment Refusal/legislation & jurisprudence , Blood Transfusion/ethics , Patient Dropouts/legislation & jurisprudence
14.
Am J Bioeth ; 11(4): 3-12, 2011 Apr.
Article in English | MEDLINE | ID: mdl-21480063

ABSTRACT

Current orthodoxy in research ethics assumes that subjects of clinical trials reserve rights to withdraw at any time and without giving any reason. This view sees the right to withdraw as a simple extension of the right to refuse to participate all together. In this paper, however, I suggest that subjects should assume some responsibilities for the internal validity of the trial at consent and that these responsibilities should be captured by contract. This would allow the researcher to impose a penalty on the subject if he were to withdraw without good reason and on a whim. This proposal still leaves open the possibility of withdrawing without penalty when it is in the subject's best interests to do so. Giving researchers recourse to legal remedy may now be necessary to protect the science, as existing methods used to increase retention are inadequate for one reason or another.


Subject(s)
Clinical Trials as Topic/ethics , Contracts/ethics , Informed Consent/ethics , Patient Dropouts/legislation & jurisprudence , Research Personnel/ethics , Research Subjects/legislation & jurisprudence , Researcher-Subject Relations/ethics , Ethics Committees, Research , Ethics, Research , Freedom , Humans , Patient Rights/ethics , Physician-Patient Relations/ethics , Reproducibility of Results , Research Personnel/legislation & jurisprudence , Volunteers
20.
J Law Med Ethics ; 38(4): 840-6, 2010.
Article in English | MEDLINE | ID: mdl-21105947

ABSTRACT

Most codes of research ethics and the practice of Institutional Review Boards (IRBs) allow human subjects to withdraw from research at any time. Consent forms invariably make a statement to this effect. So understood, a subject's right to withdraw from research is inalienable; she cannot, through her consent, surrender this right. Recently critics have argued that in selected circumstances the right to withdraw from research is alienable; subjects have the moral authority, through their consent, to obligate themselves not to withdraw. Two kinds of cases have been cited to support this. In one case, there will be great benefits lost if subjects are permitted to withdraw before the completion of the protocol. In the other case, there will be harm to third parties if subjects withdraw from the experiment. In this paper, I defend the inalienability of the right to withdraw from research. I argue, first, that securing the desired benefits and avoiding the feared harms can be achieved without allowing waiver. Second, I show that permitting waiver in these cases does not guarantee that the ends sought will be achieved. And third, I articulate positive reasons for conceiving subjects' right to withdraw from research as inalienable.


Subject(s)
Human Experimentation/ethics , Human Rights , Informed Consent/ethics , Research Subjects , Codes of Ethics , Human Experimentation/legislation & jurisprudence , Humans , Informed Consent/legislation & jurisprudence , Moral Obligations , Patient Dropouts/legislation & jurisprudence , Transplantation, Heterologous , United States
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