Ïé ïñïèåôéêïß åîïìïëïãïýíôáé

Óôåßëôå ìáò ôçí éóôïñßá óáò (áí åßóáóôå ïñïèåôéêïß) ìÝóù ôçò öüñìáò ðïõ èá âñåßôå óôï ôÝëïò áõôÞò ôçò óåëßäáò êáé åìåßò èá ôçí äçìïóéåýóïõìå.

Ìïéñáóôåßôå ôéò åìðåéñßåò óáò, ôéò áíçóõ÷ßåò óáò, ôéò åõôõ÷éóìÝíåò óáò óôéãìÝò (ãéáôß óßãïõñá õðÜñ÷ïõí êáé ôÝôïéåò óå áõôÞ ôçí ðåñéðÝôåéá ðïõ ëÝãåôáé HIV/AIDS).

Äéçãçèåßôå ìáò ôç óôéãìÞ ðïõ ï ãéáôñüò óáò áíáêïßíùóå üôé Ý÷åôå ìïëõíèåß ìå ôïí éü HIV, ôéò óõíèÞêåò ðåñßèáëøÞò óáò. Ðåßôå ìáò ãéá ôç óôéãìÞ ðïõ ôï åêìõóôçñåõôÞêáôå óôïõò äéêïýò óáò áíèñþðïõò, Þ áí êÜðïéïò óáò êïßôáîå ðáñÜîåíá üôáí Ýìáèå üôé åßóôå HIV èåôéêüò/Þ.


ÃñÜøôå åäþ ôçí éóôïñßá óáò

Äåí õðÜñ÷åé üñéï ëÝîåùí. Ìðïñåßôå íá óôåßëåôå üóï ìåãÜëåò éóôïñßåò èÝëåôå, áñêåß íá áðïöýãåôå ôçí áíáöïñÜ óå óõãêåêñéìÝíá öõóéêÜ Þ íïìéêÜ ðñüóùðá êáé êáôáóôÜóåéò ðïõ öùôïãñáößæïõí Üôïìá Þ õðçñåóßåò õãåßáò. ÓõìðåñéëÜâåôå êáé ôá áñ÷éêÜ óáò Þ Ýíá øåõäþíõìï ãéá ôïí ôßôëï ôçò éóôïñßáò óáò.

Ôï www.hivaids.gr äéáôçñåß ôï äéêáßùìá íá áöáéñÝóåé áðïóðÜóìáôá áðü ôéò éóôïñßåò ðïõ äåí áêïëïõèïýí ôïõò ðáñáðÜíù êáíüíåò.


Lancet

Ðñüóöáôåò äçìïóéåýóåéò óôï ðåñéïäéêü The Lancet HIV

Optimised second-line regimens in the public health approach

Globally, most people receive antiretroviral therapy (ART) in programmes that follow the WHO-recommended public health approach, using a small number of standard regimens and simplified monitoring.1 A single standard regimen—dolutegravir (an integrase strand transfer inhibitor [INSTI]) with tenofovir disoproxil fumarate and lamivudine (both nucleoside reverse transcriptase inhibitors, [NRTIs])—is currently taken by the large majority of people on ART in these programmes, including those on second-line therapy (following previous failure of a non-NRTI regimen).

Prioritising HIV drug resistance testing according to risk

Tenofovir–lamivudine–dolutegravir (TLD) is recommended as an initial treatment regimen and a preferred optimised regimen for people living with HIV without a history of previous viral non-suppression, referred to as TLD in first-line therapy (TLD-1). For people living with HIV with persistent viral non-suppression, TLD largely replaced protease inhibitor-based regimens following efavirenz-based initial regimens, referred to as TLD in second-line therapy (TLD-2), as it is at least as effective, better tolerated, and more affordable.

Ending paediatric AIDS: time to close implementation gaps

WHO's global health sector strategies on HIV, conceived to guide the health sector in implementing strategically focused responses to achieve the goals of ending AIDS by 2030, target a reduction in the number of children aged 0–14 years newly infected with HIV from 150 000 in 2022 to 20 000 in 2025 and 15 000 in 2030.1 To track progress toward these targets, accurate estimations of the number of annual infections in children in each country is crucial. However, in many low-income and middle-income countries, where the burden of paediatric HIV is the highest, children are not systematically tested for HIV in programmes for the prevention of vertical transmission (PVT).

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Óôï hivaids.gr, öéëïîåíïýìå áöéëïêåñäþò ôï "Ðñüãñáììá Óõíåñãáóßáò" ÌïíÜäùí Ëïéìþîåùí ãéá ôçí áíÜðôõîç äéáäéêôõáêÞò ôñÜðåæáò êëéíéêþí ðáñáìÝôñùí. Ôï Ðñüãñáììá äçìéïõñãÞèçêå áðü Ýíáí ãéáôñü åéäéêü óôçí HIV ëïßìùîç ìå ôç óõììåôï÷Þ ôùí ÌïíÜäùí: Ðåñéóóüôåñá

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