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However, patients taking the symptomatic medication when the headache was intense exhibited lower PPTs than those taking the medication at the beginning of the attack (all, P<0.05).
One hundred and thirty-six (80%) reported use of symptomatic medication for headache (73% NSAIDs); 58 (43%) took the medication at the beginning of headache whereas 78 (57%) took the medication when the headache intensity was intense.
This study found that the use of symptomatic medication intake was not related to clinical and widespread pressure pain sensitivity in TTH, but it seems that consuming symptomatic medication at the beginning of the headache could be related to lower widespread pressure pain sensitivity.
All patients did not receive any specific pulmonary artery medication at the beginning of the study.
All of the children were outpatients, and none were using medication at the beginning of the study.
Moreover, newly graduated physicians declare they are unprepared to safely prescribe medication at the beginning of their residency year [ 8, 9].
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Changes in the medication lists will be measured by comparing the patients' medication lists at the beginning and end of the intervention period.
More precisely, we a) evaluated the theoretical, practical medication and decision-making competences of the students, b) evaluated the overall medication competence of the students, and c) identified factors associated with medication competence at the beginning and at the end of their education.
The factors associated with students' medication competence at the beginning of education are mainly related to prior and current academic success, but the impact is less significant at the end of the education.
Our aim was therefore to evaluate the theoretical, practical and decision-making competence of nursing students and to identify factors associated with their medication competence at the beginning and end of their education.
We found that better medication persistence at the beginning of imatinib therapy (≧ 18 months) was associated with a longer treatment duration during the follow-up and prior therapies with hydroxyurea and IFNα (or Ara-C).
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