Untitled

CHECKLIST FOR PRESCRIBERS – COMBINED HORMONAL
CONTRACEPTIVES
Please use this checklist in conjunction with the Summary of Product
Characteristics during combined hormonal contraceptive (CHC)
consultations.

 Thromboembolism (e.g. deep vein thrombosis, pulmonary embolism, heart attack and stroke) is a rare but important risk with use of a CHC.  A woman’s risk will also depend on her baseline risk of thromboembolism. The decision to use a CHC should therefore take into consideration the contraindications and a woman’s risk factors, particularly those for thromboembolism – see boxes below and the Summary of Product Characteristics.  The risk of a thromboembolism with a CHC is higher: when re-starting use after an intake break of 4 or more weeks.  CHCs that contain ethinylestradiol in combination with levonorgestrel, norgestimate or norethisterone are considered to have the lowest risk of venous thromboembolism (VTE).  The decision to use any CHC should be taken only after a discussion with the o the effect of any intrinsic risk factors on her risk of thrombosis o the risk of thromboembolism with her CHC o that she must be alert for signs and symptoms of a thrombosis
Do not prescribe a CHC if you tick any of the boxes in this section. Does
the woman have:

Current or personal history of a thromboembolic event e.g. deep vein thrombosis, pulmonary embolism, heart attack, stroke, transient ischaemic attack, angina pectoris? Knowledge of predisposition for a blood clotting disorder? Diabetes mellitus with vascular complications? Very high blood pressure eg systolic ≥160 or diastolic ≥100mm Hg? Major surgery or a period of prolonged immobilisation coming up? If so, advise to use a different method of contraception for at least 4 weeks beforehand and two weeks after full ambulation.
Discuss the suitability of a CHC with the woman if you tick any of the
boxes in this section:

Is she a smoker? If yes and also over the age of 35 she should be strongly advised to stop smoking or use a different method of contraception. Does she have high blood pressure eg systolic 140-159 or diastolic 90-99mm Hg? Does she have a close relative (eg parent or sibling) who has had a thromboembolic event (see above list) at a young age (eg before 50)? Does she or someone in her immediate family have high blood lipids? Does she have a cardiovascular condition such as atrial fibrillation, arrhythmia, coronary heart disease, cardiac valve disease? Has she given birth in the last six weeks? Does she travel for more than 4 hours per day? Does she have any other medical conditions that might increase the risk of thrombosis (eg. cancer, systemic lupus erythematosus, sickle cell disease, Crohn’s disease, ulcerative colitis, haemolytic uraemic syndrome)? Is she taking any other medicines that can increase the risk of thrombosis (eg. corticosteroids, neuroleptics, antipsychotics, antidepressants, chemotherapy etc)? More than one of the above risk factors may mean a CHC should not be
used.
Don’t forget, a woman’s risk factors may change over time and should be
revisited at regular intervals.

Please make sure your patient understands that she should tell a
healthcare professional she is taking a combined hormonal contraceptive
if she:

 Needs to have a period of prolonged immobilisation (eg because of an injury or illness, or if her leg is in a cast)  In these situations it would be best to discuss whether a different method of contraceptive should be used until the risk of VTE returns to normal. Please also tell your patient that the risk of a blood clot is increased if
she:

 Travels for extended periods (eg during long-haul flights)
 Develops one or more of the above risk factors for VTE
 Has given birth within the last few weeks
 In these situations your patients should be particularly alert for any signs Please advise your patient to tell you if any of the above situations change or
get much worse.

Please strongly encourage women
to read the Patient Information Leaflet that
accompanies each pack of CHC. This includes the symptoms of blood clots that
she must watch out for.
Please report any adverse events suspected to be caused by a combined
contraceptive to the company or the MHRA
(http://yellowcard.mhra.gov.uk/)

Source: http://www.msd-uk.com/Style%20Library/CountrySite/UK/English/pdf/CAS%20-%20CHCs%20review%20Jan%202014%20FINAL-revised%20270114-PRESCRIBER%20CHECKLIST.PDF

Paed2002-progbk.cdr

The Overactive Bladder C. DEFOURNEY, E. VAN LAECKE, A. RAES, J. DEHOORNE, G. MOSIELLO, M.L. CAPITANUCCI, P. MASTRACCI, M. MOSCONI, Paediatric Uro- Nephrologic Centre (PUNC), Ghent University Pediatric Surgery, Urodynamic Unit, Bambino Gesù Children's LONG TERM OUTCOME OF TREATMENT OF NON NEUROPATHIC IS STOLLER AFFERENT NERVE STIMULATION (SANS) USEFUL AND BLADDER SPHINCTER DYSFUNCTION (NN

Lettera

LETTERA novembre 2010 diffusione, l’assunzione del Relpax® aveva tolto la nausea. L’esame neurologico era nella norma. La PA era 135/80. L’EMG confermava una Sindrome del Tunnel Carpale bilaterale. La paziente mi sembrava una persona concreta, per DI NEUROLOGIA E NEUROFISIOLOGIA ULSS 5 ARZIGNANO (VI) cui feci come un patto in cui si impegnava a sospendere in Sinflex®

Copyright 2014 Pdf Medic Finder