Table 1.
Inclusion criteria | Exclusion criteria | |
---|---|---|
Population/patients | Human subjects | Animals |
18 years or older | Children | |
Patients with diagnosed primary hypothyroidism or subclinical hypothyroidism | Pregnant women/patients with secondary or tertiary hypothyroidism/hyperthyroid patients/patients previously treated for thyroid cancer | |
Receiving levothyroxine treatment | Other forms of hormone replacement therapy/combination therapy | |
Intervention | Interventions of any type, intensity and frequency, with length greater than 6 weeks used to investigate effect of clinical, behavioural or pharmcogenomic factors on levothyroxine therapy | N/A |
Comparators/control | A control or comparative group is necessary. This can be placebo/no treatment/standard therapy/usual care/alternative treatment | No control/comparative group |
Outcome | Primary outcome; quantitative effect of clinical/behavioural/pharmacogenomic factors on TSH levels Secondary outcome (s); quantitative effect of clinical/behavioural/ Pharmacogenomics factors on T4 and T3 levels/any short term effects/mortality/morbidity/quality of life/treatment complications/adverse effects/rate of relapse/physical functioning/social functioning |
Reviews only focused on the quantitative effect of clinical/behavioural/ Pharmacogenomics factors on T4 and T3 levels |
Study design | RCTs, case-control studies, cohort studies, observational studies, cross sectional studies, longitudinal studies, case studies | N/A |