| مستخلص: |
This second article in the series on screening for sickle cell disorders (SCDs) looks at midwife educational needs, and whether they are equipped to deal with clients with SCDs. Their awareness and understanding of SCD may be influenced by misconception and ignorance surrounding ethnic minority needs. The need for equity of care, including the importance of trained genetic counsellors is also addressed. The lack of such specialised services outside of larger inner cities is proof of inequality of service for the population in need outside these areas. The summary of findings concludes that midwives' overall knowledge of SCD is poor and this ultimately affects their understanding of screening protocols, and the issues surrounding ethnicity. [ABSTRACT FROM AUTHOR] |