Further research to confirm the mechanism of the effect of HIV on

Further research to confirm the mechanism of the effect of HIV on sperm is vital, and further prospective studies that delineate the effects of different antiretrovirals, over longer durations of use, on semen parameters and outcome may

aid in decision-making. “
“Introduction Summary of recommendations Patient involvement in care Screening, prevention and immunisation Antiretroviral therapy Selleckchem GS1101 Hepatitis B (HBV) Hepatitis delta (HDV) Hepatitis C (HCV) Hepatitis E End-stage liver disease Acknowledgements List of Abbreviations List of Appendices The purpose of these guidelines is to provide guidance on best clinical practice in the treatment and management see more of adults with HIV and viral hepatitis coinfection. The scope includes: i) guidance on diagnostic and fibrosis screening; ii) preventative measures including immunisation and behavioural intervention; iii) ARV therapy and toxicity; iv) management of acute and chronic HBV/HIV and HCV/HIV; v) monitoring and management of coinfection-related end-stage liver disease (ESLD) including transplantation; and vi) discussion on HDV/HIV and HEV/HIV infection. The guidelines are aimed at clinical professionals involved in

and responsible for the care of adults with HIV and viral hepatitis coinfection, and at community advocates responsible for promoting the best interests and care of adults with coinfection. They should be read in conjunction with other published BHIVA and hepatitis guidelines. BHIVA revised and updated the Association’s guideline development manual in 2011 [1]. BHIVA Carnitine palmitoyltransferase II has adopted the modified Grading of Recommendations Assessment, Development and Evaluation (GRADE) system for the assessment, evaluation and grading of evidence and the development of recommendations [2–3]. The guideline was developed by a Writing Group comprising professional group members and an elected community representative. The scope, purpose and

guideline topics were agreed by the Committee and key questions concerning each guideline topic were drafted (Table 1.1) and a systematic literature review undertaken by an information scientist. Full details of the guideline development process are outlined in the appendices to this document. Review questions were developed in a PICO (patient, intervention, comparison and outcome) framework. This framework guided the literature-searching process, critical appraisal and synthesis of evidence, and facilitated the development of recommendations by the Guideline Writing Group. Eleven review questions were identified. Full literature searches and critical appraisals were completed for all specified questions.

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