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R1.2 Paediatrics—In paediatric patients, we suggest evaluating the severity of AKI by using the criteria of the pRIFLE classification.
To determine how aggressive care near the end of life really is, however, we suggest evaluating newly started chemotherapy alongside ongoing treatment.
We underline that this score has never been validated in clinical real life and therefore we suggest evaluating QsQ in further clinical trials to validate it.
Thus, we suggest evaluating educational interventions aimed at encouraging doctors to address perceived pressures and anxieties openly and to inform patients about the benign nature of the condition.
To improve the service in the future, we suggest evaluating the service regularly in joint meetings of GPs and cardiologists, to discuss potential adaptations of criteria for referral and wishes for the communication of results.
As there are promising results from both in vitro and in vivo studies, we suggest evaluating the antiosteoporotic potential by clinical trials with pomegranate fruit extract that has no side effects on uterine endometrium alongside a significant decrease in bone turn-over rate.
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In addition, we would suggest evaluating the possible correlation between tumour diameter and cross-sectional vessel enlargement or assessing the differences between various types of breast cancer, i.e. invasive versus in situ cancers.
However, our results suggest evaluating other modifiable risk factors for pancreatic cancer.
Buyse et al (2000a) suggest evaluating surrogacy by estimating two coefficients of determination; Rtrial based on data from the trials and the Rindiv based on individual patients.
This suggests evaluating the consequences of vitamin B12 deficit in PD patients under Levodopa therapy.
This suggests evaluating whether vitamin B12 deficit could aggravate the PD in patients under Levodopa therapy by impairing S-adenosylmethionine synthesis in substantia nigra.
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