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1.
Indian J Med Ethics ; 2019 OCT; 4(4): 294
Artigo | IMSEAR | ID: sea-195251

RESUMO

During the last five years, globally, cases of polio caused by vaccine viruses have outnumbered those of polio caused by natural (wild) polioviruses, posing a moral dilemma. Public health ethics should ensure the best interests of the community, with equity in sharing benefits and risks irrespective of socioeconomic disparities. Vaccine viruses in oral polio vaccine (OPV) cause vaccine-associated paralytic polio (VAPP), while paralytic polio is also caused by vaccine-derived polioviruses (VDPVs). By its policy of the use of OPV in low and middle-income countries, while rich countries use the safe inactivated polio vaccine (IPV), the Global Polio Eradication Programme has been responsible for social injustice. In 2017 and 2018, there were outbreaks of polio in Syria and Papua New Guinea due to circulating VDPVs, after many years of these countries remaining free of polio due to wild polioviruses. The only ethical way forward for global polio eradication is to replace OPV with IPV in all countries.

2.
Indian J Med Ethics ; 2019 JAN; 4(1): 26-28
Artigo | IMSEAR | ID: sea-195221

RESUMO

Medical ethics is invoked for immunisation of children as it involves an interaction between a healthcare professional and the child. Immunisation under the national immunisation programme is a public health intervention and the common belief is that ethics is not relevant. Two vaccines with contrasting safety and efficacy profiles were available against polio before the national immunisation programme was launched: the inactivated poliovirus vaccine (IPV) and the live attenuated oral poliovirus vaccine (OPV). India chose OPV and excluded IPV. We carried out an ethical appraisal of that choice. Principles of medical ethics comprising four elements—non-maleficence, beneficence, autonomy and justice—was already in vogue at the time. Applying each of them, a head-to-head comparison between IPV and OPV is made. The results clearly show that the choice of vaccine was made without using ethical principles, resulting in serious adverse effects in hundreds of thousands of children. We recommend that medical ethics must be applied to all choices of public health interventions

3.
Indian Pediatr ; 2018 Aug; 55(8): 659-660
Artigo | IMSEAR | ID: sea-199137
4.
Indian Pediatr ; 2016 May; 53(5): 399-402
Artigo em Inglês | IMSEAR | ID: sea-178997
5.
Indian Pediatr ; 2015 Oct; 52(10): 906
Artigo em Inglês | IMSEAR | ID: sea-172203
6.
Indian Pediatr ; 2015 Aug; 52(8): 717
Artigo em Inglês | IMSEAR | ID: sea-171916
7.
Indian Pediatr ; 2015 May; 52(5): 424-425
Artigo em Inglês | IMSEAR | ID: sea-171470
8.
Indian Pediatr ; 2015 Apr; 52(4): 350-351
Artigo em Inglês | IMSEAR | ID: sea-171388
9.
Indian Pediatr ; 2014 Nov; 51(11): 937-938
Artigo em Inglês | IMSEAR | ID: sea-170935
10.
Indian Pediatr ; 2014 Nov; 51(11): 869-870
Artigo em Inglês | IMSEAR | ID: sea-170889
11.
Indian Pediatr ; 2014 July; 51(7): 523-527
Artigo em Inglês | IMSEAR | ID: sea-170674

RESUMO

In spite of being the pioneer-leader of research into epidemiology and prevention of tuberculosis among low-income countries, India has the highest population-based burden of tuberculosis among all nations. Children with latent tuberculosis are the pool from which adult pulmonary tuberculosis emerges many years later. In the absence of primary prevention of infection by BCG, sociologic/behavioral interventions must be applied to reduce air-borne transmission. In addition to maximizing passive surveillance of adult disease, pediatric tuberculosis must also be brought under surveillance. Those with latent tuberculosis must be detected and treated to remove them from the pool. Epidemiologically, the realistic monitoring method of tuberculosis control trajectory is documenting progressive reduction of the short incubation period pediatric disease through surveillance, and not the reduction of long incubation period adult pulmonary tuberculosis. Application of scientific tools for the detection and management of pediatric tuberculosis infection – latent and active – holds the key to effective tuberculosis control.

12.
Artigo em Inglês | IMSEAR | ID: sea-148120

RESUMO

India's success in eliminating wild polioviruses (WPVs) has been acclaimed globally. Since the last case on January 13, 2011 success has been sustained for two years. By early 2014 India could be certified free of WPV transmission, if no indigenous transmission occurs, the chances of which is considered zero. Until early 1990s India was hyperendemic for polio, with an average of 500 to 1000 children getting paralysed daily. In spite of introducing trivalent oral poliovirus vaccine (tOPV) in the Expanded Programme on Immunization (EPI) in 1979, the burden of polio did not fall below that of the pre-EPI era for a decade. One of the main reasons was the low vaccine efficacy (VE) of tOPV against WPV types 1 and 3. The VE of tOPV was highest for type 2 and WPV type 2 was eliminated in 1999 itself as the average per-capita vaccine coverage reached 6. The VE against types 1 and 3 was the lowest in Uttar Pradesh and Bihar, where the force of transmission of WPVs was maximum on account of the highest infant-population density. Transmission was finally interrupted with sustained and extraordinary efforts. During the years since 2004 annual pulse polio vaccination campaigns were conducted 10 times each year, virtually every child was tracked and vaccinated - including in all transit points and transport vehicles, monovalent OPV types 1 and 3 were licensed and applied in titrated campaigns according to WPV epidemiology and bivalent OPV (bOPV, with both types 1 and 3) was developed and judiciously deployed. Elimination of WPVs with OPV is only phase 1 of polio eradication. India is poised to progress to phase 2, with introduction of inactivated poliovirus vaccine (IPV), switch from tOPV to bOPV and final elimination of all vaccine-related and vaccine-derived polioviruses. True polio eradication demands zero incidence of poliovirus infection, wild and vaccine.

13.
Artigo em Inglês | IMSEAR | ID: sea-144787

RESUMO

Background & objectives: Extensively drug resistant tuberculosis (XDR-TB) has become a new threat for the control of TB in many countries including India. Its prevalence is not known in India as there is no nation-wide surveillance. However, there have been some reports from various hospitals in the country. Methods: We have reviewed the studies/information available in the public domain and found data from 10 tertiary care centres in 9 cities in India. Results: A total of 598 isolates of XDR Mycobacterium tuberculosis have been reported in the studies included. However, the reliability of microbiological methods used in these studies was not checked and thus the XDR-TB data remained invalidated in reference laboratories. Interpretation & conclusions: Systematic surveillance and containment interventions are urgently needed.


Assuntos
Interpretação Estatística de Dados , Farmacorresistência Bacteriana Múltipla , Tuberculose Extensivamente Resistente a Medicamentos/epidemiologia , Tuberculose Extensivamente Resistente a Medicamentos/etiologia , Tuberculose Extensivamente Resistente a Medicamentos/prevenção & controle , Humanos , Índia/epidemiologia , Mycobacterium tuberculosis , Centros de Atenção Terciária
14.
Indian Pediatr ; 2012 October; 49(10): 787
Artigo em Inglês | IMSEAR | ID: sea-169488
15.
Indian Pediatr ; 2012 April; 49(4): 335
Artigo em Inglês | IMSEAR | ID: sea-169313
16.
Indian Pediatr ; 2012 February; 49(2): 95-98
Artigo em Inglês | IMSEAR | ID: sea-169190
17.
Indian Pediatr ; 2011 December; 48(12): 985-986
Artigo em Inglês | IMSEAR | ID: sea-169053

RESUMO

We retrospectively studied clinical and etiological profile of acute bacterial meningitis in hospitalized children for two consecutive years at a pediatric hospital in western Uttar Pradesh. Etiological diagnosis could be made in 30 (44.8%) out of 67 cases with either culture or latex agglutination test. Pneumococcus was the commonest pathogen found in 17 (25. 4%) cases. The overall mortality was 10. 5%.

19.
Indian Pediatr ; 2011 October; 48(10): 823-824
Artigo em Inglês | IMSEAR | ID: sea-169001
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