Table 7.
Family history |
|
• |
Hypertension |
• |
Cardiovascular and cerebrovascular disease |
• |
Diabetes mellitus |
• |
Dyslipidemia |
• |
Obesity |
• |
Hereditary renal disease (Polycystic kidney disease) |
• |
Hereditary endocrine disease (pheochromocytoma, adrenal hyperplasia, multiple endocrine neoplasia , von Hippel-Lindau) |
• |
Syndromes associated with hypertension (neurofibromatosis) |
Clinical history |
|
• |
Perinatal history: birth weight, gestational age, oligohydramnios, anoxia, umbilical artery catheterization |
• |
Previous history: urinary tract infection, renal or urological disease, cardiac, endocrine (including diabetes) or neurological disease, growth retardation |
• |
Symptoms suggestive of secondary hypertension: dysuria, thirst/polyuria, nocturia, hematuria, edema, weight loss, failure to thrive, palpitations, sweating, fever, pallor, flushing, cold extremities, intermittent claudication, virilization, primary amenorrhea, male pseudohermaphroditism |
• |
Symptoms suggestive of target organ damage: headache, epistaxis, vertigo, visual impairment, facial palsy, fits, strokes, dyspnea |
• |
Sleep history: snoring, apnea, daytime somnolence |
• |
Risk factor history: low physical exercise level, incorrect dietary habits, smoking, alcohol, licorice |
• |
Drug intake: cyclosporine, tacrolimus, tricyclic anti-depressants, antipsychotics, decongestants, oral contraceptives, illegal drugs |
• | Pregnancy |
Lurbe et al. “Management of High Blood Pressure in Children and Adolescents: recommendations of the ESH”. Journal of Hypertension 2009 [2] (modified).