Presentation is loading. Please wait.

Presentation is loading. Please wait.

Data from the Collaborative HIV Paediatric Study (CHIPS) Reports up to June 2015* * Numbers are based on reports received rather than children seen to.

Similar presentations


Presentation on theme: "Data from the Collaborative HIV Paediatric Study (CHIPS) Reports up to June 2015* * Numbers are based on reports received rather than children seen to."— Presentation transcript:

1 Data from the Collaborative HIV Paediatric Study (CHIPS) Reports up to June 2015* * Numbers are based on reports received rather than children seen to the end of June 2015. 2014/15 data are subject to reporting delay and may therefore be incomplete.

2 Background to CHIPS The Collaborative HIV Paediatric Study (CHIPS) was established in April 2000 and is a multi-centre cohort study of HIV-1 infected children in the UK and Ireland. The collaboration is between – 67 clinics in the UK and Ireland that care for HIV-infected children – the National Study of HIV in Pregnancy and Childhood (NSHPC), and – the MRC Clinical Trials Unit at UCL

3 Follow-up status of 1934 children enrolled in CHIPS * 94 deaths prior to 2008, 6 in 2008, 6 in 2009, 2 in 2010, 2 in 2011

4 Age group by year first presented to medical services in the UK/Ireland (1926*) * Includes all children (those still in follow-up and those who have died, lost to follow-up, left the UK & Ireland or transferred to adult care) Up to 2010 2011 2012 2013 2014+ Total At birth 172 (10%) 5 (8%) 4 (13%) 0 (0%) 3 (14%) 184 (10%) <1 yr 302 (17%) 2 (3%) 2 (6%) 0 (0%) 1 (5%) 307 (16%) 1-4 yrs 523 (29%) 7 (11%) 2 (6%) 6 (30%) 4 (18%) 542 (28%) 5-9 yrs 473 (26%) 10 (16%) 10 (31%) 4 (20%) 6 (27%) 503 (26%) 10-14 yrs 287 (16%) 28 (44%) 14 (44%) 6 (30%) 8 (36%) 343 (18%) >=15 yrs 31 (2%) 12 (19%) 0 (0%) 4 (20%) 0 (0%) 47 (2%) Total 1788 (100%) 64 (100%) 32 (100%) 20 (100%) 22 (100%) 1936 (100%)

5 Year No. Median (IQR) ------------------------- Age group ------------------------ age < 1 yr 1-4 yrs 5-9 yrs 10-14 yrs 15-19 yrs ≥20 yrs 1996 333 4.7 (2.5-7.1) 33(10%) 146(44%) 124(37%) 30(9%) 0(0%) 0(0%) 1997 382 5.1 (2.6-7.9) 47(12%) 141(37%) 148(39%) 45(12%) 1(0%) 0(0%) 1998 456 5.5 (2.8-8.4) 38(8%) 171(38%) 178(39%) 64(14%) 5(1%) 0(0%) 1999 528 6.1 (3.2-9.3) 32(6%) 180(34%) 209(40%) 95(18%) 12(2%) 0(0%) 2000 623 6.7 (3.6-10.0) 35(6%) 193(31%) 240(39%) 129(21%) 26(4%) 0(0%) 2001 712 7.4 (4.3-10.6) 34(5%) 194(27%) 276(39%) 168(24%) 40(6%) 0(0%) 2002 815 7.8 (4.7-11.4) 37(5%) 191(23%) 320(39%) 206(25%) 60(7%) 1(0%) 2003 954 8.3 (5.3-11.8) 35(4%) 179(19%) 389(41%) 265(28%) 81(8%) 5(1%) 2004 1076 8.8 (5.8-12.5) 32(3%) 188(17%) 408(38%) 321(30%) 114(11%) 13(1%) 2005 1185 9.5 (6.3-13.2) 33(3%) 169(14%) 437(37%) 362(31%) 158(13%) 26(2%) 2006 1274 10.2 (6.8-13.9) 30(2%) 160(13%) 434(34%) 404(32%) 208(16%) 38(3%) 2007 1361 10.9 (7.4-14.5) 25(2%) 138(10%) 414(30%) 475(35%) 251(18%) 58(4%) 2008 1439 11.7 (8.2-15.3) 18(1%) 132(9%) 365(25%) 536(37%) 304(21%) 84(6%) 2009 1508 12.5 (9.1-16.2) 17(1%) 118(8%) 338(22%) 541(36%) 370(25%) 124(8%) 2010 1552 13.4 (9.9-17.0) 10(1%) 94(6%) 293(19%) 570(37%) 409(26%) 176(11%) 2011 1606 14.3 (10.8-17.8) 10(1%) 73(5%) 250(16%) 572(36%) 462(29%) 239(15%) 2012 1629 15.2 (11.7-18.8) 7(0%) 48(3%) 218(13%) 523(32%) 533(33%) 300(18%) 2013 1644 16.1 (12.6-19.7) 3(0%) 38(2%) 188(11%) 437(27%) 596(36%) 382(23%) 2014 1656 17.0 (13.5-20.7) 2(0%) 29(2%) 155(9%) 390(24%) 593(36%) 487(29%) Age of UK/Irish cohort of patients with HIV acquired in childhood, 1996-2014 Note: Data are for all children and young people alive who were ever in follow-up from 1996 onwards, including children who have since transferred to adult care; those who subsequently died or were lost to follow-up are excluded from the year of death or loss to follow-up. All paediatric infections are included, regardless of mode of acquisition (94% perinatal). CHIPS includes all diagnosed HIV-infected children known to be living in the UK/Ireland, of whom ~50% were born abroad. Data for 2014 are incomplete as subject to reporting delay.

6 Age of UK/Irish cohort of patients with HIV acquired in childhood, 1996-2014 N= 333 456 623 815 1076 1274 1439 1552 1629 1656 382 528 712 954 1185 1361 1508 1606 1644

7 Year No. Median (IQR) ------------------------- Age group ------------------------ age < 1 yr 1-4 yrs 5-9 yrs 10-14 yrs 15-19 yrs ≥20 yrs 1996 35 5 (2-7) 1(3%) 16(46%) 13(37%) 5(14%) 0(0%) 0(0%) 1997 32 3.5 (1-6.5) 6(19%) 12(38%) 11(34%) 2(6%) 1(3%) 0(0%) 1998 52 4.5 (1-8) 3(6%) 23(44%) 17(33%) 8(15%) 1(2%) 0(0%) 1999 204 6 (3-9) 11(5%) 66(32%) 88(43%) 35(17%) 4(2%) 0(0%) 2000 279 6 (3-10) 6(2%) 112(40%) 87(31%) 61(22%) 13(5%) 0(0%) 2001 259 5 (3-8) 3(1%) 126(49%) 78(30%) 41(16%) 11(4%) 0(0%) 2002 261 5 (3-7) 7(3%) 119(46%) 103(39%) 26(10%) 6(2%) 0(0%) 2003 352 5 (3-7) 11(3%) 122(35%) 169(48%) 42(12%) 8(2%) 0(0%) 2004 452 6 (4-8) 11(2%) 143(32%) 230(51%) 57(13%) 10(2%) 1(0%) 2005 572 7 (4-9) 10(2%) 134(23%) 321(56%) 90(16%) 16(3%) 1(0%) 2006 608 7 (5-9) 10(2%) 122(20%) 361(59%) 98(16%) 16(3%) 1(0%) 2007 644 8 (6-10) 4(1%) 109(17%) 335(52%) 180(28%) 15(2%) 1(0%) 2008 733 9 (6-11) 10(1%) 106(14%) 325(44%) 270(37%) 22(3%) 0(0%) 2009 775 9 (7-12) 1(0%) 91(12%) 299(39%) 340(44%) 44(6%) 0(0%) 2010 832 10 (8-13) 1(0%) 77(9%) 245(29%) 448(54%) 57(7%) 4(0%) 2011 870 11 (8-13) 5(1%) 57(7%) 216(25%) 481(55%) 106(12%) 5(1%) 2012 894 12 (9-14) 1(0%) 37(4%) 192(21%) 449(50%) 206(23%) 9(1%) 2013 924 13 (10-15) 0(0%) 26(3%) 167(18%) 408(44%) 307(33%) 16(2%) 2014 955 14 (11-16) 2(0%) 22(2%) 129(14%) 357(37%) 410(43%) 35(4%) Note: Data are for all children and young people alive who were ever in follow-up from 1996 onwards, including children who have since transferred to adult care; those who subsequently died or were lost to follow-up or transferred to adult care are excluded from the year of death or loss to follow-up or transfer. All paediatric infections are included, regardless of mode of acquisition (94% perinatal). CHIPS includes all diagnosed HIV-infected children known to be living in the UK/Ireland, of whom ~50% were born abroad. Data for 2014 are incomplete as subject to reporting delay. Age of UK/Irish cohort of patients with HIV acquired in childhood & seen in paediatric care, 1996-2014

8 Note: Data are for all children and young people alive who were ever in follow-up from 1996 onwards, including children who have since transferred to adult care; those who subsequently died or were lost to follow-up or transferred to adult care are excluded from the year of death or loss to follow-up or transfer. All paediatric infections are included, regardless of mode of acquisition (94% perinatal). CHIPS includes all diagnosed HIV-infected children known to be living in the UK/Ireland, of whom ~50% were born abroad. Data for 2014 are incomplete as subject to reporting delay. N= 35 52 279 261 452 608 733 832 894 955 32 204 259 352 572 644 775 870 924

9 All hospital admissions during 2000-2013 * Retrospective data on admissions not collected for children from clinics joining since Aug 2003. These children are counted from when they begin prospective follow-up in CHIPS. Admissions may be underreported for children in shared care where only information from the main CHIPS follow-up clinic is reported. Data for 2013 are incomplete as subject to reporting delay. 2000 629 161 25.6 320 51.5 2001 717 170 23.7 300 42.7 2002 814 156 19.2 241 29.9 2003 947 178 18.8 309 33.2 2004 1048 177 16.9 281 27.5 2005 1130 176 15.6 287 25.9 2006 1198 164 13.7 245 20.9 2007 1247 145 11.6 215 17.6 2008 1274 145 11.4 213 17.2 2009 1278 119 9.3 152 12.4 2010 1246 95 7.6 139 11.4 2011 1247 111 8.9 152 12.8 2012 1155 72 6.2 88 8.0 2013 1069 55 5.1 64 6.8 Year Number Number Proportion Total Rate (# children children admitted number admissions seen* admitted (%) admissions per 100 pyr)

10 Year Viral load (copies/ml) ≤50 or ≤lower assay limit*** 1997/1999 26/101 (26%) 2000/2004 133/338 (39%) 2005/2009 259/417 (62%) 2010- 179/238 (75%) Total 597/1094 (55%) * Response is based on the viral load value nearest 12 months (+/-3 months) after cART initiation ** Newly defined as: first line therapy is 3 or more drugs across two classes or 3NRTIs including ABC ***46/597 (8%) of undetectable results had a lower limit of detection >50 but ≤400c/ml and are included here. Viral load suppression 12 months * after starting cART naïve**, all ages N=1094 with measurements available

11 Year Viral load (copies/ml) ≤50 or ≤lower assay limit*** 1997/1999 22/93 (24%) 2000/2004 119/305 (39%) 2005/2009 195/326 (60%) 2010- 99/133 (74%) Total 435/857 (51%) * Response is based on the viral load value nearest 12 months (+/-3 months) after cART initiation ** Newly defined as: first line therapy is 3 or more drugs across two classes or 3NRTIs including ABC *** 36/435 (8%) of undetectable results had a lower limit of detection >50 but ≤400c/ml and are included here. Viral load suppression 12 months * after starting cART naïve**, at age ≤12 years N=857 with measurements available

12 Year Viral load (copies/ml) ≤50 or ≤lower assay limit*** 1997/1999 4/8 (50%) 2000/2004 14/33 (42%) 2005/2009 64/91 (70%) 2010- 80/105 (76%) Total 162/237 (68%) * Response is based on the viral load value nearest 12 months (+/-3 months) after cART initiation ** Newly defined as: first line therapy is 3 or more drugs across two classes or 3NRTIs including ABC *** 10/162 (6%) of undetectable results had a lower limit of detection >50 but ≤400c/ml and are included here. Viral load suppression 12 months * after starting cART naïve**, at age ≥13 years N=237 with measurements available

13 Time to viral rebound (>1000c/ml) for children suppressing viral load ≤400c/ml within 12 months of starting cART naïve, 2000-2005

14 Time to viral rebound (>1000c/ml) for children suppressing viral load ≤400c/ml within 12 months of starting cART naïve, 2006-2013

15 1 Response is based on viral load value closest to 12 months (+/-3 months) after starting 1st/ 2nd line, for those starting cART naive and remaining on 1st line for at least 12 months and 2nd line for at least 12 months. 2 Defined as any switch across drug class or change/addition of PI drug or addition of new drug class. 3 98/434 had missing viral load after 12 months on 1st line, and a further 88/434 had missing viral load after 12 months on 2nd line. 4 22 (5%) undetectable results had a lower limit of detection >50 but ≤400c/ml and are included. Year starting 2 nd - line cART Number (%) ≤50c/ml or ≤lower assay limit 4 12 months after starting.... 1 st line cART2 nd line cART 1997/20003/13 (23%)4/11 (36%) 2001/200314/50 (28%)29/46 (63%) 2004/200624/67 (36%)47/77 (61%) 2007/200946/81 (57%)60/89 (67%) 2010-73/125 (58%)100/133 (75%) Total 160/336 (48%)240/356 (67%) Viral load 12 months 1 after starting 1st and 2nd line cART for those switching 2 to 2nd line ( N=434 children switched to 2 nd line after at least 12 months on 1 st line 3 )

16 Data on 979 children who are in active follow-up Those who have died, lost to follow-up, left the UK & Ireland or transferred to adult care are excluded.

17 Demographics (N=979) (Data provided by NSHPC) 516 (53%) are female 471 (48%) born UK/Ireland, 485 (50%) born abroad (not known for 21 children) Ethnicity: Diagnosis of maternal infection (N=906 vertically infected): White 56(6%) Black African 760(78%) Black other 8(1%) Indian 13(1%) Mixed 98(10%) Other 12(1%) Not known 32(3%) Known after delivery743(82%) Known before delivery131(14%) Not known32(4%)

18 462 (48%) London 41 (4%) Scotland 404 (41%) Rest of England 52 (5%) Ireland 12 (1%) Wales Regional distribution of main follow-up clinic for 979 children alive and followed up in CHIPS Children who have died, lost to follow-up, left the UK & Ireland or transferred to adult care are excluded 5 (<1%) Northern Ireland

19 Year of last follow-up (N=956)

20 Clinical stage by age at last follow-up (N=956) No. of children< 2 years2-4 years5-9 years10-14 years≥15 yearsTotal(%) Stage N/A 5(83%)22(73%)94(59%)211(51%)149(43%) 481(50%) Stage B 1(17%)4(13%)27(17%)105(26%)117(33%) 254(27%) Stage C 0(0%)4(13%)39(24%)94(23%)84(24%) 221(23%) Total 6(100%)30(100%)160(100%)410(100%)350(100%)956(100%)

21 Antiretroviral drug experience N=905 children with follow-up since January 2013 No. of children < 2 years2-4 years5-9 years10-14 years≥15 yearsTotal(%) Naive 0(0%)3(12%)17(11%)42(11%)15(4%) 77(9%) 1-4 drugs 4(80%)13(50%)69(45%)143(37%)82(24%) 311(34%) 5-7 drugs 1(20%)10(38%)56(37%)123(32%)119(35%) 309(34%) 8+ drugs 0(0%)0 10(7%)74(19%)124(36%) 208(23%) Total 5(100%)26(100%)152(100%)382(100%)340(100%)905(100%)

22 ART at last follow-up N=828 children with follow-up since Jan 2013 were on treatment 28 on mono, 44 on dual, 700 on 3-drug, 52 on 4-drug and 4 on 5(+)-drug therapy

23 Most recent CD4% (N=832) Children followed up since January 2013 No. of children 0-10%11-20%21-30%>30%Total Naïve 0(0%)18(25%)26(36%)28(39%)72(100%) On mono 0(0%)3(14%)11(50%)8(36%)22(100%) On dual 1(2%)7(16%)12(28%)23(53%)43(100%) On initial cART 0(0%)17(6%)84(32%)163(62%)264(100%) On subseq cART 5(1%)32(8%)107(27%)251(64%)395(100%) Off ART 2(6%)7(19%)17(47%)10(28%)36(100%) Note: Row percentages now provided. Initial cART newly defined as first line therapy is 3 or more drugs across two classes or 3NRTIs including Abacavir. Subsequent cART defined as any switch across drug class or change/addition of PI drug or addition of new drug class.

24 Most recent CD4 count (N=828) Children ≥ 5 years old followed up since Jan 2013 No. of children 0-200201-350351-500501-1000>1000Total Naïve 0(0%)5(7%)15(21%)39(56%)11(16%)70(100%) On mono 1(4%)5(21%)4(17%)10(42%)4(17%)24(100%) On dual 2(5%)5(12%)3(7%)17(41%)14(34%)41(100%) On initial cART 0(0%)10(4%)35(13%)177(67%)43(16%)265(100%) On subseq cART 10(3%)23(6%)51(13%)205(52%)102(26%)391(100%) Off ART 3(8%)8(22%)8 15(41%)3(8%)37(100%) Note: Row percentages now provided. Initial cART newly defined as first line therapy is 3 or more drugs across two classes or 3NRTIs including Abacavir. Subsequent cART defined as any switch across drug class or change/addition of PI drug or addition of new drug class.

25 No. of chcaildren ≤50c/ml (or ≤lower assay limit**) >50c/ml (or>lower assay limit) – 100,000c/ml >100,000c/mlTotal Naïve 2(3%)71(95%)2(3%)75(100%) On mono 14(61%)9(39%)0(0%)23(100%) On dual 30(75%)10(25%)0(0%)40(100%) On initial cART 241(87%)35(13%)0(0%)276(100%) On subseq cART 326(82%)69(17%)1(1%)396(100%) Off ART 7(17%)28(68%)6(17%)41(100%) Most recent viral load (N=851) Children followed up since January 2013 Note: Row percentages now provided. Initial cART newly defined as first line therapy is 3 or more drugs across two classes or 3NRTIs including Abacavir. Subsequent cART defined as any switch across drug class or change/addition of PI drug or addition of new drug class. **6/620 ( 50 but ≤400c/ml and are included here.

26 Outcome 1: Retention in care Percentage of newly diagnosed children in 2012 who had ≥2 CD4 and ≥2 VL measurements within 12 months of diagnosis Notes: The y axis shows percentages, and at the top of each bar shows the number of children

27 Outcome 2: Retention on ART Percentage of patients newly starting ART in 2011 who were still on ART in 2012 Notes: The y axis shows percentages, and at the top of each bar shows the number of children

28 Outcome 3A: Immune status in children <5 yrs Percentage of children aged <5 years with ≥1 CD4 measure ≥25% in 2012, by ART status Notes: The y axis shows percentages, and at the top of each bar shows the number of children

29 Outcome 3B: Immune status in children ≥5 years Percentage of children aged ≥5 years with ≥1 CD4 measure ≥350 cells/mm 3 in 2012, by ART status Notes: The y axis shows percentages, and at the top of each bar shows the number of children

30 Outcome 4A: Virological response on ART Percentage of children on ART with ≥2 VL measures <50c/ml and <400c/ml, in 2012 Notes: The y axis shows percentages, and at the top of each bar shows the number of children Dotted bar: VL <400c/ml Plain bar: VL <50 c/ml

31 Outcome 4B: Virological response on ART, age≥13yrs Percentage of young people aged ≥13 years on ART with ≥2 VL measures <50c/ml, and <400 c/ml, in 2012 Notes: The y axis shows percentages, and at the top of each bar shows the number of children Dotted bar: VL <400c/ml Plain bar: VL <50 c/ml

32 Outcome 5: Description of deaths in 2011 One paediatric death was previously reported to CHIPS in 2011: The patient died whilst in paediatric care in the South London network with causes of death given as "acute liver failure" and "septic shock". This child presented aged 2 years with a CD4% of 21% and CD4 count of 323c/ml. This child died aged 2 years and had been in follow up for less than a year, and had been seen twice in the 12 months prior to their death. This patient is not known to have taken any ART drugs. One paediatric death in 2011 has since been reported to CHIPS: The patient died whilst in paediatric care in the North London network with causes of death given as “CMV pneumonitis". This child presented aged 1 year and 6 months with a CD4% of 1% and CD4 count of 68c/ml. This child died aged 1 year and 7 months and had been in follow up for a month, and had been seen once. This patient is not known to have taken any ART drugs.

33 Outcome 5: Description of deaths in 2012 No paediatric deaths in 2012 have been reported to CHIPS.

34 Involvement in PENTA trials Some patients from CHIPS are currently involved in BREATHER (PENTA 16). For further details about BREATHER please contact mrcctu.penta@ucl.ac.uk.penta@ucl.ac.uk Centres with patients in BREATHER Evelina – 3 St George’s – 4 GOSH - 7 Leicester – 2Nottingham – 1 Birmingham – 4Bristol – 1 Dublin – 3 Recent PENTA publications/presentations: Harrison L., Melvin A., Fiscus S., Saidi Y., Nastouli E., Harper L., Compagnucci A., Babiker A., McKinney R., Gibb D., Tudor-Williams G., HIV-1 Drug Resistance and Second-line Treatment in Children Randomized to Switch at Low versus Higher RNA Thresholds, JAIDS 2015 Sep 1;70(1). Once- versus twice-daily lopinavir/ritonavir in HIV-1 infected children: a randomised controlled trial (KONCERT/PENTA18/ANRS150). Accepted for publication in AIDS ART with weekends off is non-inferior to continuous ART in young people on EFV+2NRTI; Karina Butler on behalf of the PENTA 16 (BREATHER) trial team, Conference on Retroviruses and Opportunistic Infections, Seattle Feb 23-26 th 2015, Abstract 38LB Freguja R, De Rossi A, Poulson H, Klein N, Del Bianco P,, Compagnucci, A, Saidi Y, Giaquinto C, Harper L, Gibb D on behalf of the PENTA Steering Committee: Long-term consequences of planned treatment interruption in HIV-1-infected children. CROI 2015, Seattle, USA, Feb 23 -26 2015. Poster presentation abstract 919. Seeley J on behalf of the Bernays S, Paparini S, Namukwaya Kihika S, Rhodes T and the BREATHER Trial Team. “But it’s my story”: exploring the experience and effect of telling children how they have acquired HIV; 3 rd International ASSHH Conference, Stellenbosch, South Africa, 6-9 July 2015. Paparini S on behalf of Bernays S, Seeley S, Rhodes T, Namukwaya Kihika S, Kawuma-Kigawa R, Nakyambadde H, Kabajaasi O and the BREATHER Trial Team. Young people, clinical trials and ‘the HIV experience’: What can similarities across time and place tell us about growing up with HIV? 3 rd International ASSHH Conference, Stellenbosch, South Africa, 6-9 July 2015. Bernays S, Seeley J, Paparini S, Rhodes T and the ARROW and BREATHER trial teams ‘I am scared of getting caught up in my lie’: challenges to self-reported adherence for young people living with HIV; accepted for presentation at AIDS Impact, Amsterdam 28-31 July, 2015 (abstract 3435) Bernays S, Seeley J, Paparini S, Rhodes T and the BREATHER trial teams ‘I was like, oh my God, what happens if it doesn’t work’?: young people living with HIV, clinical trial participation, and the truth economy accepted for presentation at BSA Medical Sociology Conference, York, 9-11 September 2015 (Paper ID No: W0012148).

35 Recent CHIPS-related publications / presentations (based either wholly or partly on CHIPS data) Childs T, Shingadia D, Goodall R, Doerholt K, Lyall H, Duong T, Judd A, Gibb DM, Collins IJ. Outcomes after viral load rebound on first-line antiretroviral therapy in HIV-infected children in the UK/ Ireland: an observational cohort study. Lancet HIV, Vol 2 No 4, e151-e158, April 2015. Payne H, Judd A¸ Donegan K, Okike IO, Ladhani S, Doerholt K, Heath PT. Incidence of pneumococcal and varicella disease in HIV-infected children and adolescents in the UK and Ireland, 1996-2011: two potentially vaccine- preventable infections. Pediatric Infectious Disease Journal 2015; 34(2): 149-154. Duong T, Judd A, Collins J, Doerholt K, Lyall H, Foster C, Butler K, Tookey P, Shingadia D, Menson E, Dunn DT, Gibb DM. Long-term virological outcome in children on antiretroviral therapy in the UK and Ireland. AIDS 2014; 28(16): 2395-2405. Hussain N, Lewis J, Childs T, Judd A, Klein N, Fidler K. To investigate the number of UK paediatric HIV patients with persistently low CD4 counts despite antiretroviral therapy. 21 st Annual Conference of the British HIV Association, Brighton 2015 (poster presentation). Patel A, Judd A, Foster C, Welch S, Menson E, Lim E, Klein N, Fidler K. To determine the prevalence of HIV seroreversion across 6 collaborating paediatric HIV centres in the UK. 21 st Annual Conference of the British HIV Association, Brighton 2015 (oral presentation). Herbert S, Barbour A, Judd A, Jungmann E, Foster C on behalf of the HIV Young People’s Network (HYPNET). Malignancy in HIV positive young people. 21 st Annual Conference of the British HIV Association, Brighton 2015 (poster presentation).

36 Acknowledgements We thank the families and staff at hospitals which participate in CHIPS. CHIPS is funded by the NHS (London Specialised Commissioning Group), and has received additional support from Bristol-Myers Squibb, Boehringer Ingelheim, GlaxoSmithKline, Roche, Abbott, and Gilead. For further information on CHIPS, please visit: www.chipscohort.ac.uk


Download ppt "Data from the Collaborative HIV Paediatric Study (CHIPS) Reports up to June 2015* * Numbers are based on reports received rather than children seen to."

Similar presentations


Ads by Google