Sentence examples for disease data collection from inspiring English sources

The flow of infectious disease data collection is shown in Figure  1.

At the calibration sessions, first a review of the techniques for caries and periodontal disease data collection was provided to the examiners.

For example, the activities supporting the development of a Malaria Surveillance Database in Swaziland were categorized as burden of disease data collection rather than design and development of HMIS.

Another observation was that overall reporting progress has improved, delay in publication of EBOV testing results dropped from 20 to 2 years, and a model of standardized wildlife disease data collection terminology was recently developed by the USAID PREDICT project (39).

Whilst this review identified common practices such as home visits, assessment and treatment of disease, data collection, education and counselling and referrals, it did at a high level of generality, signalling categories of work but providing few details about the processes involved.

In order to predict the future burden of oral disease, as well to identify potential interventions to reduce the burden of these diseases, data collection and reporting standards are needed to ensure that data is consistently collected and used effectively to inform policy, prevention and control activities for health [ 20].

To actually describe the individual course in a fluctuating condition such as inflammatory rheumatic diseases, data collection at regular and tight intervals are needed [ 10, 11].

Application of these results would depend on trial setting, population, disease area, data collection and follow-up procedures.

Application of the findings of this review would depend on trial setting, population, disease area, data collection and follow-up procedures.

Of these 13 declined further investigation with small intestinal biopsy and 41 had a normal biopsy, leaving 238 children (137 girls) with undetected celiac disease at data collection.

Recently, the Direcção-Geral de Saúde (DGS) [ 21], under the National Program for Rare Diseases, commenced data collection for a nationwide registry for these rare diseases via the distribution of the "Rare Disease Patient Card"; therefore, it is expected that in the near future, an effective and accurate national database will be accessible.