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Although 1 mg/kg furosemide was used in the original paper for FST [21, 23], furosemide dose administered in our study was different in each patient and was determined by the physician based on the patient's condition.
These are the cases with injuries not considered to have any medico-legal implications by the physician based on the circumstances that led to the injury such as injuries sustained due to a fall at home caused by a slippery surface.
One eye per patient was selected as the study eye by the physician based on the inclusion/exclusion criteria.
Data on medication and diabetes complications were registered with the use of a standardized questionnaire, which was completed by the physician based upon medical files.
Pain was assessed by the physician based on the patient's medical history according to Hideo Watanabe's knee scoring system-related pain score [ 37].
The cases were classified as primary or secondary infections by the physician based on hemagglutination assays performed on different DV serotypes and on Japanese encephalitis virus.
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This study was designed and undertaken by the physicians based in the renal unit at the University Hospital Birmingham in collaboration with the department of clinical immunology at the University of Birmingham.
In the end, the decision has to be made by the treating physician based on the algorithm recommendations and the judgement of the patients.
The dosage was determined by the treating physician based on the Summary of Product Characteristics (SmPC) that recommends therapeutic FXI levels of approximately 30 40% (0.3 0.4 IU mL−1 of plasma).
Evaluation plans were designed and determined by the evaluating physician based on the presenting symptom complex.
Data on medication and risk factors were registered by the attending physician based upon the medical files.
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