आईएसएसएन: 2161-0711

सामुदायिक चिकित्सा एवं स्वास्थ्य शिक्षा

खुला एक्सेस

हमारा समूह 1000 से अधिक वैज्ञानिक सोसायटी के सहयोग से हर साल संयुक्त राज्य अमेरिका, यूरोप और एशिया में 3000+ वैश्विक सम्मेलन श्रृंखला कार्यक्रम आयोजित करता है और 700+ ओपन एक्सेस जर्नल प्रकाशित करता है जिसमें 50000 से अधिक प्रतिष्ठित व्यक्तित्व, प्रतिष्ठित वैज्ञानिक संपादकीय बोर्ड के सदस्यों के रूप में शामिल होते हैं।

ओपन एक्सेस जर्नल्स को अधिक पाठक और उद्धरण मिल रहे हैं
700 जर्नल और 15,000,000 पाठक प्रत्येक जर्नल को 25,000+ पाठक मिल रहे हैं

में अनुक्रमित
  • सूचकांक कॉपरनिकस
  • गूगल ज्ञानी
  • शेरपा रोमियो
  • जेनेमिक्स जर्नलसीक
  • सेफ्टीलिट
  • RefSeek
  • हमदर्द विश्वविद्यालय
  • ईबीएससीओ एज़
  • ओसीएलसी- वर्ल्डकैट
  • पबलोन्स
  • चिकित्सा शिक्षा और अनुसंधान के लिए जिनेवा फाउंडेशन
  • यूरो पब
  • आईसीएमजेई
इस पृष्ठ को साझा करें

अमूर्त

Genetics in Primary Healthcare in Brazil: Potential Contribution of Mid-level Providers and Community Health Workers

Gramasco HHF, Baptista FH, Ribeiro MG, de Avó LRS, Germano CMR and Melo DG

Objective: This study aimed to investigate genetic care competencies of mid-level health providers and community health workers in Brazil.

Methods: It is a descriptive survey study, whereby mid-level health providers (nursing auxiliaries and technicians, and auxiliaries in oral health) and community health workers were invited to participate by answering a questionnaire including 10 structured genetics-oriented issues. Data were presented as percentages. Differences between groups were assessed by the Fisher exact test, with the level of significance set at p<0.05.

Results: Concerning knowledge, most of the participants valued important aspects of family history like the distribution of a disease over successive generations and presence of consanguinity, and 79% of them recognized that there are families at increased risk of developing cancers. They also had good knowledge about exposure to teratogens and neonatal screening. Regarding clinical skills, practitioners were able to recognize facial dysmorphias and 63% showed predisposition to gather information about genetic disease in the family history. Regarding attitudes, 65% believed that patients with rare diseases require interdisciplinary approach and 61% showed initiative to refer patients for specialist. In general, there was no significant difference between both professional groups on the investigated knowledge, skills and attitudes, except for the skill to distinguish the phenotype of Down and Crouzon syndromes, which was more present among the mid-level health providers (p 0.04).

Conclusion: These findings may contribute to developing an ongoing education program for mid-level health providers and community health workers, leading to a strategy to overcome the challenges of integrating genetics into primary healthcare in Brazil.