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1.
Ethics Int Aff ; 35(4): 543-562, 2021.
Article in English | MEDLINE | ID: mdl-34937990

ABSTRACT

COVID-19 vaccines are likely to be scarce for years to come. Many countries, from India to the U.K., have demonstrated vaccine nationalism. What are the ethical limits to this vaccine nationalism? Neither extreme nationalism nor extreme cosmopolitanism is ethically justifiable. Instead, we propose the fair priority for residents (FPR) framework, in which governments can retain COVID-19 vaccine doses for their residents only to the extent that they are needed to maintain a noncrisis level of mortality while they are implementing reasonable public health interventions. Practically, a noncrisis level of mortality is that experienced during a bad influenza season, which society considers an acceptable background risk. Governments take action to limit mortality from influenza, but there is no emergency that includes severe lockdowns. This "flu-risk standard" is a nonarbitrary and generally accepted heuristic. Mortality above the flu-risk standard justifies greater governmental interventions, including retaining vaccines for a country's own citizens over global need. The precise level of vaccination needed to meet the flu-risk standard will depend upon empirical factors related to the pandemic. This links the ethical principles to the scientific data emerging from the emergency. Thus, the FPR framework recognizes that governments should prioritize procuring vaccines for their country when doing so is necessary to reduce mortality to noncrisis flu-like levels. But after that, a government is obligated to do its part to share vaccines to reduce risks of mortality for people in other countries. We consider and reject objections to the FPR framework based on a country: (1) having developed a vaccine, (2) raising taxes to pay for vaccine research and purchase, (3) wanting to eliminate economic and social burdens, and (4) being ineffective in combating COVID-19 through public health interventions.

3.
Infect Chemother ; 53(3): 572-577, 2021 Sep.
Article in English | MEDLINE | ID: mdl-32869551

ABSTRACT

Disseminated adenovirus infections (d-ADV) after hematopoietic cell transplant (HCT) are often fatal with limited treatment options. Brincidofovir (BCV) a lipid ester of cidofovir is developed for this indication. We report four pediatric HCT recipients with d-ADV treated successfully with BCV.

4.
Med Mycol ; 58(8): 1029-1036, 2020 Nov 10.
Article in English | MEDLINE | ID: mdl-32171012

ABSTRACT

We sought to describe the clinical experience of voriconazole as primary antifungal prophylaxis (AFP) in allogeneic hematopoietic cell transplant recipients (allo-HCTr). This was a single-center retrospective study of adult allo-HCTr (1 January 2014 to 31 December 2016) who received ≥two doses of voriconazole-AFP. Voriconazole-AFP was started on day +7 post-HCT and continued at least through day +60 post-HCT, or longer as clinically indicated. We reviewed the rate, reasons, and risk factors of voriconazole-AFP discontinuation until day-100 post-HCT. A total of 327 patients were included. Voriconazole-AFP was continued for a median of 69 days (mean: 57.9; range 1, 100): for a median of 90 days (mean :84; range 2, 100) in 180/327 (55%) in the standard-of-care (SOC) group and 20 days (mean :25.6 ; range 1, 89; P-value < .001) in 147/327 (45%) patients in the early-discontinuation-group. Early-voriconazole-AFP discontinuation was due to adverse events, drug interactions, insurance coverage, and other reasons in 101/147 (68.7%), 27 (18.4%), 13 (8.8%), and 6 (4.1%) patients, respectively. Early-voriconazole-AFP discontinuation occurred in 73/327 (22.3%) patients due to hepatotoxicity. Important predictors for early-voriconazole-AFP discontinuation included: graft-versus-host disease grade ≥2 (odds ratio [OR]: 1.9, P-value: .02), alanine-aminotransferase ≥75 IU/ml on voriconazole-administration day-14 (OR: 5.6, P-value: .02) and total bilirubin ≥1.3 mg/dl on voriconazole-administration day-7 (OR: 3.0, P-value: .03). There were 13 proven/probable invasive fungal infections by day-180 post-HCT (8/147, 5.4%, and 5/180, 2.8% in the early-discontinuation and SOC-groups, respectively; log-rank:0.13). By day-180 post HCT, 23/147 (15.6%) and 14/180 (7.8%) patients in the early-discontinuation and SOC-groups had died, respectively (log-rank:0.03). Voriconazole-AFP was discontinued in up to 45% of allo-HCTr. Hepatotoxicity during the first 2 weeks post-HCT is a significant predictor of early-voriconazole-AFP discontinuation.


Subject(s)
Antibiotic Prophylaxis/statistics & numerical data , Antifungal Agents/therapeutic use , Hematopoietic Stem Cell Transplantation , Voriconazole/therapeutic use , Adult , Antibiotic Prophylaxis/adverse effects , Antifungal Agents/adverse effects , Chemical and Drug Induced Liver Injury/epidemiology , Chemical and Drug Induced Liver Injury/physiopathology , Female , Hematopoietic Stem Cell Transplantation/adverse effects , Humans , Invasive Fungal Infections/epidemiology , Invasive Fungal Infections/prevention & control , Male , Middle Aged , Retrospective Studies , Risk Factors , Transplant Recipients , Transplantation, Homologous , Treatment Outcome , Voriconazole/adverse effects
7.
J Adv Nurs ; 66(5): 1022-34, 2010 May.
Article in English | MEDLINE | ID: mdl-20337794

ABSTRACT

AIM: This paper is a report of a pilot study conducted to investigate the effect of a tailor-made ergonomic intervention programme for community nurses. BACKGROUND: The nursing profession is known to be a high risk group for work-related musculoskeletal disorders. Community nurses are at risk as they have to travel to patients' homes and work in varied environments daily. Their occupational risk factors are unique and intervention strategies need to be specially designed to address these issues. METHOD: The study was conducted from August 2007 to September 2008 in Hong Kong with community nurses from three hospitals. The intervention group (n = 14) received a multi-faceted ergonomic intervention programme over an 8-week period, with group training, onsite individual training, equipment modification, exercise programme, typing and computer workstation advice. The control group (n = 12) received no interventions. Both groups had baseline and follow-up assessments, which included musculoskeletal symptoms, perceived risk factors and functional outcome and physical mobility measures. RESULTS: The intervention group showed statistically significantly improved symptom scores and neck and upper limb functional outcomes at postintervention. The control group showed no change in symptom or functional outcomes. CONCLUSION: A multifaceted intervention programme may be more effective than interventions that mainly focus on ergonomic training and could be considered by community or home care nursing groups in other countries. The programme was based on risk assessment and may be a useful reference for other nursing groups in other countries.


Subject(s)
Community Health Nursing , Ergonomics , Nursing Staff/education , Occupational Diseases/prevention & control , Occupational Health Services/organization & administration , Adult , Consumer Behavior , Female , Focus Groups , Hong Kong , Humans , Inservice Training , Male , Middle Aged , Musculoskeletal Diseases/prevention & control , Nursing Staff/psychology , Occupational Diseases/etiology , Pilot Projects , Program Evaluation , Risk Factors , Safety Management/organization & administration , Stress, Psychological/prevention & control , Workload , Young Adult
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