Table 7 |
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Variables used in quantifying quality of records |
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Variable 1 |
Therapeutic approach of the issue patient, in the context of the given PCU |
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Variable 2 |
Laboratory data, in relation to the laboratory facilities of the given PCU |
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Variable 3 |
Community Approach: interrelation between patient's disease and primary care services |
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Variable 4 |
Family record: complete genogram or family pedigree, as well as record of existing dynamics within the family |
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Variable 5 |
Patient assessment: Prioritising of diagnostic problems and differential diagnosis (organisation of data), as well as the proposed steps and further measures needed for disease management within the primary care services |
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Variable 6 |
Management Strategy or Plan: Services suggested by the medical personnel of the PCU for the best possible management of the patient within the primary care services |
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Variable 7 |
Utility or Usefulness of primary care: Information related to the parts of the management plan that were actually implemented at the PCU and to the way this implementation offered positive or negative feedback to the PCU |
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9 and 10 |
All criteria covering the biopsychosocial point of view, as defined by Prof. Howard F. Stein [14], and in particular: |
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Variable 8 |
Information on "Who", i.e. about the subject-person (the way the patient perceives his/her disease or medical condition, and the effects on the patient's relationship with the other members of the family and the community) [3] |
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Variable 9 |
Information on "What", i.e. about the disease – illness – sickness perception of the subject, and the effects it has on the biological, functional and social level respectively |
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Variable 10 |
Information on "Where", i.e. data on the environment of the patient, and on how this environment affected the patient's medical condition or health problem [24-26] |
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Belos et al. BMC Medical Education 2005 5:13 doi:10.1186/1472-6920-5-13 |
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