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There remain some localised areas of high prevalence for which local control measures will be required.
Indication characteristics included data on the type of disease and disease prevalence for which the product is indicated.
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Hence, this overall prevalence is reported for any location, in addition to location-specific prevalences for which the responses on neck and shoulders were combined (neck/shoulder), as were those on arms/elbows and hands/wrists (upper extremity).
According to Martin et al. [ 4], this value is called design prevalence, and it describes the prevalence assumption for which the sensitivity estimate of the SSC is valid.
These diseases include certain infections that share a common mode of transmission with HIV, diseases whose onset is favoured by HIV-induced immunodeficiency, and any other medical condition associated with an undiagnosed HIV prevalence greater than 0.1%, the prevalence value for which delivering routine HIV testing resulted to be cost-effective [ 11, 12].
In conclusion, Eurolight should not be seen as a primary source of prevalence estimates, for which it was neither intended nor designed.
In the United States, the term rare or orphan disease is defined by the Orphan Drug Act as a condition affecting fewer than 200,000 people in the country, or one with a greater prevalence but for which no reasonable expectation exists that the costs of developing and distributing a drug can be recovered from the sale of the drug in the United States.
56 57 Existing multivariable regression analyses using RDS samples have not appropriately addressed the co-relation between observations and the unequal sampling probabilities inherent in RDS; therefore, we have focused on reporting prevalence estimates for which methods are better established.
At present, multivariable regression analyses using RDS samples have not appropriately addressed the co-relation between observations and the unequal sampling probabilities inherent in RDS; therefore, we present prevalence estimates for which methods are better established.
Particularly in populations with a low HIV prevalence, and for which further confirmatory testing may not be available, the use of a third POCT device is recommended to minimise any risk of false positive diagnoses.[ 38] It is important to select POCT devices that are highly sensitive and specific, easy to perform and whose end-point reaction is easily read.
This is similar to the prevalence for Africa which is 21% and the 2012 study from China of 24%[17]], but much lower than that of the global estimate which was 46%[4].
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