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The objective of the article was to assess methodologies published and applied in calculating mortality attributable to smoking. A review of the literature was made for the period 1990 to 2006, in the electronic databases MEDLINE and LILACS. A total of 186 studies were found, which measured mortality based on calculating the smoking-attributable risk. Of these, a total of 41 were selected. The studies that were carried out in the United States and Canada presented a more standard methodology and reported smoking attributable mortality to be 18%-23%, with male mortality being 25%-29% and female mortality 14%-17%. The variations can be attributed to methodological differences and to different estimates of the main tobacco-related illnesses.

A new species of Loimopapillosum Hargis, 1955 is described based on specimens collected from the gills of the diamond stingray, Hypanus dipterurus (Jordan & Gilbert, 1880) (Myliobatiformes: Dasyatidae) captured off Puerto Pizarro, Tumbes Region, northern Peru. Loimopapillosum pascuali n. sp. is distinguished mainly from the type and only species, Loimopapillosum dasyatis Hargis, 1955, by its funnel-shaped male copulatory organ, with an asymmetrical base; the superficial root of the anchor with distal knobs; the deep root of the anchor with a constriction at its base; a single testis; and the number of head organs. Available sequences for members of Monocotylidae in the GenBank as well as partial sequences for the gene 28S and 18S ribosomal DNA from L. pascuali n. sp. were included in phylogenetic analyses, suggesting that Loimoinae (represented in this study by L. pascuali n. sp. and Loimosina sp.) is nested within the Monocotylidae Taschenberg, 1879. Therefore, we confirm the rejection of Loimoidae Price, 1936 and its reincorporation as a subfamily of Monocotylidae, as previously suggested. Loimopapillosum pascuali n. sp. represents the first species of this genus in South America.

Intestinal cryptosporidiosis is a diarrheal disease caused by protists of genus Cryptosporidium that infect a wide variety of hosts, primarily vertebrates. Due to the close contact between humans and their companion animals, especially dogs and cats, there is concern about the potential for zoonotic transmission of this enteric protozoan parasite by infected animals. This study aimed to perform a microscopic and molecular diagnosis of Cryptosporidium spp. in fecal samples from domiciled dogs and cats. One hundred and nineteen fecal samples were processed using sugar centrifugal flotation followed by molecular detection of Cryptosporidium spp. DNA using nested PCR. Subtyping of isolates positive for C. parvum was performed by sequence analysis of the 60 kDa glycoprotein gene (GP60). Cryptosporidium oocysts were detected in 7.8% (5/64) and 5.4% (3/55) of the fecal samples from dogs and cats, respectively. Cryptosporidium canis (n = 3) and C. parvum (n = 2) were the main species found in dogs, whereas C. felis (n = 3) was prevalent in cats. Subtype IIaA17G2R2 (potentially zoonotic) was identified in samples positive for C. parvum. Despite the low prevalence of Cryptosporidium observed in the domiciled dogs and cats, the presence of potentially zoonotic C. parvum in dogs evidences a public health concern. Further research is needed to better understand the epidemiology, source, and potential impacts of Cryptosporidium infection in cats and dogs.

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