AIDS and Doctors

PEDIATRICS ◽  
1989 ◽  
Vol 83 (6) ◽  
pp. A38-A38
Author(s):  
R. J. M.

Santa Monica, CA—. . .While there isn't a single documented case of a patient catching acquired immune deficiency syndrome from a doctor or other healthcare worker, medical caregivers with AIDS—and those who have tested positive for the AIDS virus but don't have the disease—raise difficult and sensitive questions for the medical community. The central question: whether these people should continue to treat and maintain contact with patients. "What you have are fundamental ethical issues of fairness, justice and moral responsibility," says Ronald Bayer, a Columbia University bioethics professor. . . As of last September 3, 182 health-care workers were known to have AIDS, including 356 physicians, according to the US Centers for Disease Control. . . most hospitals that have discovered an attending physician or health-care worker with AIDS do try to re-assign the individuals to other duties, especially if they are involved in performing invasive procedures. But. the courts have consistently held that AIDS is a physical handicap protected under state and federal anti-discrimination laws. . . . Procedures used to handle the question of what to do about doctors with AIDS will only work if these doctors identify themselves. But a handful of infected physicians have learned the hard way what happens when word of their condition leaks out. . . (After a newspaper report revealed that a Dallas-area pediatrician had AIDS last year) local medical authorities assured parents that the doctor wasn't a threat to their children. But the assurances did no good, and his practice collapsed. "Any risk is too great when you're dealing with my children," (said the parent of a patient.). . .(The pediatrician's) advice to other doctors with AIDS: "Don't tell anyone."

2020 ◽  
Vol 7 (1) ◽  
pp. 77-79
Author(s):  
Samita Acharya ◽  
Kripa Maharjan

Amid this pandemic, which has been spreading like a wildfire globally, Nepal is not an exception to it. With this, we have been hearing the news of global shortage of personal protective equipment (PPE), with growing concern over the safety of medical community and possibility of cross-contamination. Triaging is less researched and reported in COVID-19. It is as important as PPE, a gateway of safety for health care worker. If we have to manage COVID-19, ensuring triage should be among the priority strategies. Patan hospital is among the few hospitals in Nepal where triaging is practiced.


2018 ◽  
Vol 71 (4) ◽  
pp. 1934-1939
Author(s):  
Cleuma Sueli Santos Suto ◽  
Jeane Freitas de Oliveira ◽  
Mirian Santos Paiva

ABSTRACT Objective: To apprehend social representation of health care professionals on HIV/AIDS and to compare it with a subgroup of physicians. Method: Qualitative research based on the Theory of Social Representations. Free associations for the term HIV/AIDS were collected from 73 workers of public services specialized in HIV/AIDS, in Salvador-Bahia. The results were analyzed in the EVOC software. Results: For all health professionals, HIV/AIDS is associated with “prejudice, care, disease and prevention”, and for the subgroup of physicians it is associated with the term “prevention”. Health professionals represented HIV/AIDS similarly to society in general and, due to their normative character, prescribed attitudes typical of health care professionals. Final considerations: The findings show that, despite the advances in the health area regarding the treatment of AIDS, prejudice still persists. It is important to strengthen interdisciplinary actions focused on discussions on this theme during training, favoring the comprehensiveness of the assistance.


Author(s):  
Barbara Jane Holland

CRISPR (clustered regularly interspaced short palindromic repeats) technology has emerged as a powerful technology for genome editing and is now widely used in basic biomedical research to explore gene function. More recently, this technology has been increasingly applied to the study or treatment of human diseases. CRISPR/Cas9 gene editing has also been applied in immunology-focused applications such as the targeting of C-C chemokine receptor type 5, the programmed death 1 gene and the creation of chimeric antigen receptors in T cells for purposes such as the treatment of the acquired immune deficiency syndrome (AIDS) or promoting anti-tumor immunotherapy. Furthermore, scientist recently suggest through their study that CRISPR may not work for everyone. This paper will review gene editing technology and its ethical concerns.


Author(s):  
Befekadu S. Wodajo ◽  
Gloria Thupayagale-Tshweneagae ◽  
Oluwaseyi A. Akpor

Background: Stigma and discrimination attached to human immunodeficiency virus (HIV) and acquired immune deficiency syndrome (AIDS) have been recognised as a major obstacle to HIV prevention, treatment, care and support throughout the world. Stigma and discrimination are more devastating when they occur in health care settings where it is least expected.Aim: To explore the factors attributable to stigma and discrimination of people living with HIV in two Ethiopian rural hospitals on what they thought of health care professionals (HCPs) attending to them.Methods: A qualitative exploratory approach was used. Data collection was by means of audio-taped interview and Tesch’s content analysis approach was used. The sample size for this study was determined by saturation of data and consisted of 16 participants who were people living with HIV admitted as inpatients to the two selected hospitals in Amhara region of Ethiopia.Results: Participants’ views were grouped into: fear of contact, delay of services, substandard services, denial of care, impoliteness of health care providers, breach of confidentiality and poor patient follow-up for persons infected with HIV.Conclusion: The health care settings have been recognised as one of the contexts where HIV and AIDS-related stigmatisation and discrimination can occur. Hospital policies and institutional support should be tailored to embrace people living with HIV as the provision of institutional support is imperative in creating a good working environment and improving the commitment of HCPs so as to enable them to provide holistic care for people living with HIV and AIDS (PLWHA) without discrimination.


1990 ◽  
Vol 1 (4) ◽  
pp. 127-132
Author(s):  
Kevin P Browne ◽  
Steve D Shafran ◽  
John M Conly

The medical records of 19 patients with acquired immune deficiency syndrome (aids) were reviewed in an attempt to estimate their health care costs. The patients were all male, members of high risk groups and diagnosed between April 1985 and February 1988. Twelve of the patients died; they lived a mean of 240 days (range 0 to 580) after diagnosis, were admitted three times (range one to six) to hospital for 65 total days (range one to 148) for a cost per patient of $33,721 (range $2,768 to $64,981) for inpatient care. They made five (range zero to 25) office visits per patient costing $196 per patient (range $0 to $4,999) for outpatient care. The seven survivors (one was lost to follow-up) have lived 375 days (range 186 to 551) since diagnosis, have been admitted to hospital two times (range zero to seven) for 30 total days (range zero to 86) for a total cost per patient of $14,223 (range $0 to $39,410) for inpatient care. They have made 11 office/emergency room visits (range zero to 46) costing in total $4322 (range $0 to $13,605) for outpatient care. The total expenditure was $546,332 ($28,754 per patient), of which total fees to physicians were $37,210 (6.8%), and estimated costs of laboratory tests $117,917 (21.6%), drugs $36,930 (6.7%), and medical imaging $20,794 (3.8%). Patients now deceased cost $416,445 (mean $34,704 per patient), accounting for 76.2% of overall expenditures. The average medical/surgical and drug costs per patient day in hospital were greater foraidspatients than for the average medical/surgical patient in the authors’ institution.


Author(s):  
Margaret Williams ◽  
Dalena R.M. Van Rooyen ◽  
Esmeralda J. Ricks

Background: The human immunodeficiency virus and/or acquired immune deficiency syndrome (HIV/AIDS) pandemic continues to increase in prevalence worldwide, particularly in South Africa, and includes the often overlooked paediatric population. The provision of paediatric antiretroviral treatment (ART) is as essential for children as for adults, and has numerous obstacles, not least of which is lack of decentralisation of facilities to provide essential treatment. Optimising ART, care and support for HIV-positive children, and their caregivers, at public sector primary health care (PHC) clinics is crucial to improve morbidity and mortality rates in children.Aim: To explore the experiences of health care professionals regarding the provision of ART for children at PHC clinics.Setting: The study was conducted in six PHC clinics in Nelson Mandela Bay Health District, Eastern Cape, South Africa.Methodology: The researchers used a qualitative, explorative, descriptive and contextual research design with in-depth interviews. We used non-probability purposive sampling. Data collected were thematically analysed using Creswell’s data analysis spiral. We used Lincoln and Guba’s model to ensure trustworthiness. Ethical standards were applied.Results: Health care professionals experienced numerous challenges, such as lack of resources, need for training, mentoring and debriefing, all related to providing decentralised ART for HIV-positive children at the PHC level.Conclusion: Capacitation of the health care system, integration of services, competent management and visionary leadership to invoke a collaborative interdisciplinary team approach is required to ensure that HIV is treated as a chronic disease at the PHC clinic level.


Author(s):  
Kanniammal Chinnathambi ◽  
Latha Mangeswari ◽  
Jaideep Mahendra

Objective:  The  aim  of  the  study  was  to  assess  the  level  of  knowledge  among  health-care  students  (HCS)  toward  human  immunodeficiency virus/acquired immune deficiency syndrome (HIV/AIDS) and people living with HIV (PLHIV) in dental and nursing colleges at Chennai.Methods: A quantitative approach and descriptive research design were adopted for the present study. HIV knowledge questionnaire-45 was used to assess the level of knowledge regarding HIV and PLHIV. Nonprobability convenient sampling technique was used for the selection of samples.Results: The collected data were analyzed using SPSS. Among 600 HCS, 274 (46%) had inadequate knowledge, 191 (32%) had moderately adequate knowledge, and about 135 (23%) students had adequate knowledge. The mean knowledge score was 10.94.Conclusion: HCS are in need of intense teaching program with various teaching methods which help to enhance their knowledge level and to eliminate the fear and stigma about handling of PLHIV.Keywords: The health-care students, Level of knowledge, Human immunodeficiency virus/Acquired immune deficiency syndrome, People living with human immunodeficiency virus.


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