What is Martin Gardner’s argument for the objectivist view of art? Do you agree? Why or why not?
Use Vaughnâs textbook to help you explain Gardnerâs theory and its strengths and weaknesses. Choose an object, performance, or piece of writing as an example, and explain whether Gardnerâs theory would classify the object as Art. Do you agree with objectivism about Art or do you find another theory more convincing? Defend your point of view.
Sample Solution
In Pakisthan, 35.5% of the patients had negative slide for parasite but treated with antimalarial drugs, its irrational prescription of antimalarial drugs, without laboratory confirmation of malarial disease increase drug pressure in the community (Khan et al., 2012). Self-treatment was extremely common in Kenya, 60% patients treated at home with herbal remedies or medicines (Ruebush et al., 1999). Use of antimalarial treatment for febrile episodes and self-treatment are common in high malaria-endemic areas (Nwanyanwu et al.1996, Mahomva et al. 1996). Several factors were involved in the increase drug pressure in the community such Self intake of the drugs by patients (Jombo et al., 2011; Nsimba et al., 2005; Souares et al., 2009, Hodel et al.,2009& 2010), irrational treatment practices by the physician (Aborah et al., 2013; Khan et al., 2012), unawareness regarding the suitable antimalarial drug to be used for treating malaria, long acting antimalarials post treatment prophylaxis, Mass drug administration (Stepniewska &White, 2008). Increase drug pressure on the parasites as screening resistant parasite population and spread. Chapter- III Materials and methods Population screening and sample collection This study was carried-out during the year 2011-2013 at Bilaspur district in Chhattisgarh (n=70), Betul district in Madhya Pradesh (n=80), Simdega district in Jharkhand (n=73) and Sundergarh district in Odisha (n=72). The patients with Pf mono-infection, fulfilling inclusion criteria (WHO criteria, 2009) were enrolled in the study. Written and oral consent was obtained from each enrolled participant. Finger prick blood samples were used for identification and counting parasite density on day 0. Before the initiating the antimalarial drug treatment, three hanging blood drops on 3Chr Whatman filter paper and 100âl blood on 31ET filter paper for analyzing dhps gene mutation and estimating residual antimalarial or SDX level on day 7 respectively, was collected from each enrolled patient. The collected dried blood spot (DBS) papers were placed in zipper pouch and kept in desiccator till analysis. The patients >
In Pakisthan, 35.5% of the patients had negative slide for parasite but treated with antimalarial drugs, its irrational prescription of antimalarial drugs, without laboratory confirmation of malarial disease increase drug pressure in the community (Khan et al., 2012). Self-treatment was extremely common in Kenya, 60% patients treated at home with herbal remedies or medicines (Ruebush et al., 1999). Use of antimalarial treatment for febrile episodes and self-treatment are common in high malaria-endemic areas (Nwanyanwu et al.1996, Mahomva et al. 1996). Several factors were involved in the increase drug pressure in the community such Self intake of the drugs by patients (Jombo et al., 2011; Nsimba et al., 2005; Souares et al., 2009, Hodel et al.,2009& 2010), irrational treatment practices by the physician (Aborah et al., 2013; Khan et al., 2012), unawareness regarding the suitable antimalarial drug to be used for treating malaria, long acting antimalarials post treatment prophylaxis, Mass drug administration (Stepniewska &White, 2008). Increase drug pressure on the parasites as screening resistant parasite population and spread. Chapter- III Materials and methods Population screening and sample collection This study was carried-out during the year 2011-2013 at Bilaspur district in Chhattisgarh (n=70), Betul district in Madhya Pradesh (n=80), Simdega district in Jharkhand (n=73) and Sundergarh district in Odisha (n=72). The patients with Pf mono-infection, fulfilling inclusion criteria (WHO criteria, 2009) were enrolled in the study. Written and oral consent was obtained from each enrolled participant. Finger prick blood samples were used for identification and counting parasite density on day 0. Before the initiating the antimalarial drug treatment, three hanging blood drops on 3Chr Whatman filter paper and 100âl blood on 31ET filter paper for analyzing dhps gene mutation and estimating residual antimalarial or SDX level on day 7 respectively, was collected from each enrolled patient. The collected dried blood spot (DBS) papers were placed in zipper pouch and kept in desiccator till analysis. The patients >
