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Kartika Maharani
"ABSTRAK
Latar Belakang: Neuropati perifer merupakan komplikasi neurologis tersering pada pasien HIV. Stavudin, yang dikaitkan dengan risiko neuropati perifer, mulai ditinggalkan sebagai pilihan pertama terapi antiretroviral. Penelitian ini bertujuan untuk mengetahui angka kejadian neuropati pada pasien HIV dalam terapi antiretroviral non stavudin menggunakan multimodalitas pemeriksaan, dan faktor risiko yang berhubungan.
Metode Penelitian: Penelitian berdesain potong lintang menggunakan data sekunder dari penelitian JakCCANDO ditambah dengan data primer dari pasien HIV dalam terapi antiretroviral non stavudin minimal 12 bulan yang berobat di Unit Pelayanan Tepadu (UPT) HIV Rumah Sakit Umum Pusat Nasional Cipto Mangunkusumo (RSUPNCM). Anamnesis dan penelusuran data faktor risiko, skrining klinis Brief Peripheral Neuropathy Screen (BPNS), elektroneurografi, dan Stimulated Skin Wrinkling (SSW) dengan krim lidokain:prilokain 5% dilakukan pada setiap subjek penelitian. Data dianalisis dengan SPSS 17.0.
Hasil: Angka kejadian polineuropati simetris distal (PSD) pada 68 subjek penelitian berdasarkan BPNS, elektroneurografi, SSW, dan kombinasi ketiga modalitas ialah 16,2%, 25%, 29,4%, dan 52,9%. Subjek dengan CD4 nadir kurang dari 50 sel/l memiliki risiko PSD sebesar 2,85 kali lebih tinggi dibandingkan kelompok subjek dengan CD4 nadir yang lebih tinggi (IK 95% 1,99-8,29). Subjek yang memiliki tinggi badan lebih dari sama dengan 170 cm (p<0,03) dan viral load lebih dari sama dengan 35.000 kopi/ml (p<0,05) memiliki rerata kecepatan hantar saraf sensorik tungkai bawah lebih rendah dibandingkan subjek dengan tinggi badan dan viral load yang lebih rendah.
Kesimpulan: Angka kejadian neuropati perifer pada pasien HIV masih cukup tinggi yaitu 52,9% dari subjek penelitian, meskipun stavudin tidak lagi digunakan. Penggunaan multimodalitas pemeriksaan memberikan kemampuan deteksi neuropati lebih banyak dibandingkan modalitas pemeriksaan tunggal. Subjek dengan CD4 nadir kurang dari 50 sel/l, 2,85 kali lebih berisiko mengalami PSD. Penelitian ini juga menunjukkan adanya hubungan antara tinggi badan lebih dari sama dengan 170 cm dan viral load lebih dari sama 35.000 kopi/ml terhadap abnormalitas parameter elektroneurografi saraf sensorik tungkai bawah.

ABSTRACT
Background: Peripheral neuropathy was a common neurologic complications in HIV patients. Stavudine, which was often associated with neuropathy risk, is no longer used as first line HAART. This study was aimed to determine prevalence of neuropathy in HIV patients receving HAART without stavudine using multi modalities examination, and associated risk factors.
Materials and Method: A cross-sectional study was undertaken using secondary data from JakCCANDO study subjects and primary data from HIV patients receiving antiretroviral therapy without stavudine for minimum 12 months in Integrated HIV Outpatient Clinics of Cipto Mangunkusumo General Hospital. All subjects were performed history taking, Brief Peripheral Neuropathy Screen (BPNS), electroneurography, and Stimulated Skin Wrinkling (SSW) using lidocaine:prilocaine 5% cream. Data analysis was done using SPSS 17.0.
Results:Prevalence of symmetric distal polyneuropathy (DSP) from 68 study subjects based on BPNS, electroneurography, SSW, and combination of three modalities were 16,2%, 25%, 29,4%, and 52,9%. Subjects with nadir CD4 less than 50 cells/l were at increased risk of DSP 2,85 times larger than subjects with higher nadir CD4 (CI 95% 1,99-8,29). Subjects with a height of equal or more than 170 cm (p<0,03) and viral load of equal or more than 35.000 copies/ml (p<0,05) had significantly decrease mean of lower extremities sensory nerve conduction velocities based on electroneurography compared to subjects with lower height and viral load.
Conclusions: Peripheral neuropathy remained a numerous neurological complication, as much as 52,9% of study subjects, even when stavudine was no longer used. Multiple diagnostic tools used in this study gave higher neuropathy number compared to single diagnostic modality. Subjects with nadir CD4 less than 50 cells/l had 2,85 times higher risk of having DSP. There were also correlation between height equal or more than 170 cm and viral load equal or more than 35.000 copies/ml with electroneurographic parameter abnormalities of sensory nerve in lower extremities.
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Depok: Fakultas Kedokteran Universitas Indonesia, 2015
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UI - Tesis Membership  Universitas Indonesia Library
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Anyeliria Sutanto
"Latar Belakang: Neuropati perifer merupakan salah satu komplikasi neurologis yang banyak ditemui pada pasien HIV. Hal ini dapat disebabkan oleh infeksi HIV tersebut ataupun sebagai akibat efek samping terapi antiretroviral, khususnya stavudin. Manifestasi klinis neuropati sangat beragam, salah satunya ialah adanya keluhan nyeri, yang dapat mempengaruhi kualitas hidup pasien. Penelitian ini bertujuan untuk mengetahui pengaruh neuropati perifer terhadap kualitas hidup pasien HIV dalam terapi antiretroviral non-stavudin.
Metode Penelitian: Penelitian ini merupakan studi komparatif potong lintang yang melibatkan pasien HIV di RS Cipto Mangunkusumo pada bulan September 2016 hingga September 2017. Kriteria inklusi subjek ialah pasien HIV dewasa dalam terapi antiretroviral non-stavudin selama minimal 12 bulan yang akan dibagi menjadi dua kelompok, berdasarkan brief peripheral neuropathy screening tool BPNST , yaitu kelompok dengan neuropati perifer dan tanpa neuropati perifer. Penilaian depresi dengan Hamilton depression rating scale HDRS dan evaluasi kualitas hidup dengan short form-36 health survey SF-36 . Kuesioner SF-36 mencakup domain kesehatan fisik dan kesehatan mental dengan rentang skor 0-100. Skor yang lebih tinggi menunjukkan kualitas hidup yang lebih baik. Data dianalisis dengan SPSS 20.0.
Hasil: Didapatkan subjek sebanyak 29 orang pada kelompok neuropati perifer dan 58 orang pada kelompok tanpa neuropati perifer. Rentang usia subjek ialah 23-59 tahun dengan median kadar sel limfosit T CD4 yang lebih rendah 406 sel/mm3 vs. 540 sel/mm3 dan persentase riwayat terapi isoniazid yang lebih tinggi 62,1 vs. 37,9 pada kelompok neuropati perifer. Karakteristik demografis usia, jenis kelamin, pendidikan terakhir, pekerjaan, status pernikahan dan karakteristik klinis jumlah sel limfosit CD4 terakhir tidak mempengaruhi kualitas hidup pada kedua kelompok, baik dengan maupun tanpa neuropati perifer. Tidak didapatkan perbedaan skor SF-36 yang bermakna pada kedua kelompok. Tampak median skor SF-36 yang lebih rendah pada subjek dengan nyeri neuropatik pada ekstremitas bawah skor kesehatan fisik 77,5 vs. 85,31 dan depresi skor kesehatan fisik 80 vs. 94,37 dan skor kesehatan mental 75 vs 89,68 untuk kelompok neuropati, skor kesehatan fisik 78,75 vs. 90,31 dan skor kesehatan mental 70,72 vs 88,75 untuk kelompok tanpa neuropati . Viral load RNA HIV berkorelasi negatif terhadap skor SF-36 pada kelompok dengan neuropati perifer skor kesehatan fisik, rs = -0,376 dan skor kesehatan mental, rs = -0,308.
Kesimpulan: Neuropati perifer tidak mempengaruhi kualitas hidup pasien HIV dalam terapi antiretroviral non-stavudin.Kata Kunci: antiretroviral non-stavudin, HIV, kualitas hidup, neuropati perifer.

Background Peripheral neuropathy is one of the most common neurologic complications in patients with HIV, which is caused by the HIV infection itself or as the side effect of antiretroviral therapy ART , particularly the usage of stavudine. Patients with neuropathy might complain various clinical manifestations, including pain, which could significantly affect patients quality of life. Aim of this study was to evaluate the role of peripheral neuropathy to quality of life of patients with HIV receiving non stavudine antiretroviral therapy.
Materials and Method This was a cross sectional internal comparison study which were done to HIV patients in Cipto Mangunkusumo Hospital during September 2016 to September 2017. Inclusion criteria were HIV adult patients with non stavudine antiretroviral therapy for minimum of 12 months which will be divided into two groups, based on brief peripheral neuropathy screening tool BPNST , as neuropathy group and non neuropathy group. Diagnosis of depression by Hamilton depression rating scale HDRS , and evaluation of quality of life was based on 36 item short form survey SF 36 . The SF 36 assessed physical health PH and mental health MH domain with score ranged from 0 to 100, in which higher score represents better quality of life. Data was analyzed using SPSS 20.0.
Results There were 29 subjects with peripheral neuropathy and 58 subjects without peripheral neuropathy. Age of the subjects was ranging from 23 to 59 years old, with lower median of CD4 lymphocyte count 406 cells mm3 vs. 540 cells mm3 and higher percentages of isoniazid therapy 62.1 vs. 37.9 in neuropathy group. Demographic characteristics age, sex, education level, employment, marital status and clinical characteristic CD4 lymphocyte count was not affecting the quality of life, both in neuropathy group and non neuropathy group. No significant difference was found from SF 36 score in both groups. There were lower SF 36 score median in subjects with neuropathic pain in lower extremities PH score 77.5 vs. 85.31 and depression PH score 80 vs. 94.37 and MH score 75 vs 89.68 in neuropathy group, PH score 78.75 vs. 90.31 and MH score 70.72 vs 88.75 in non neuropathy group. Viral load was negatively correlated with SF 36 score in subjects with peripheral neuropathy PH score, rs 0,376 and MH score, rs 0,308.
Conclusion Peripheral neuropathy did not affect the quality of life of HIV patients receiving non stavudin antiretroviral therapy."
Depok: Universitas Indonesia, 2017
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UI - Tugas Akhir  Universitas Indonesia Library
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Fitri Octaviana
"Pendahuluan: Prevalensi neuropati sensorik HIV (NS-HIV) di RS Cipto Mangunkusumo (RSCM) pada tahun 2006 adalah 33%, saat seluruh pasien mendapatkan terapi antiretroviral (ARV) stavudine. Walaupun stavudine tidak digunakan lagi, pasien masih mengeluhkan gejala NS-HIV. Penelitian ini bertujuan untuk mengetahui prevalensi dan faktor yang berhubungan dengan NS-HIV dan nyeri neuropatik; kadar kemokin CCL5 plasma dan antibodi IgG CMV pada NS-HIV dan nyeri neuropatik. Tujuan lain adalah untuk mengetahui dan gambaran intra-epidermal nerve fiber density (IENFD) dan makrofag CD14+ perineural pada NS-HIV.
Metode: Penelitian potong lintang yang dilakukan di RSCM pada tahun 2015-2017. Didapatkan 197 pasien HIV dalam terapi ARV tanpa stavudin >12 bulan. NS-HIV ditegakkan berdasarkan The AIDS Clinical Trial Group Brief Peripheral Neuropathy Screening Tool (ACTG-BPNST/BPNST), sedangkan nyeri neuropatik dinilai menggunakan kuesioner Douleur Neuropathique 4 (DN4). Dilakukan pengambilan darah untuk mengukur hitung sel T CD4+, viral load, CCL5, antibodi IgG CMV. Dilakukan pemeriksaan nerve conduction study (NCS) dan Stimulated SkIin Wrinkle (SSW) test. Biopsi kulit dilakukan pada 9 pasien NS-HIV dan 5 pasien tanpa NS (NS-) untuk menilai intra-epidermal nerve fiber density (IENFD) dan makrofag CD14+ perineural dan dibandingkan kontrol sehat.
Hasil: Prevalensi NS-HIV adalah 14,2% sedangkan prevalensi nyeri neuropatik 6,6%. Faktor yang berhubungan dengan NS-HIV adalah viral load >500 kopi/ml dan meningkatnya usia. Faktor yang berhubungan dengan nyeri neuropatik adalah penggunaan ARV Protease Inhibitor (PI) dan durasi ARV< 2 tahun. Kadar CCL5 plasma dan antibody IgG CMV tidak berhubungan terhadap NS-HIV dan nyeri neuropatik. Median IENFD pada pasien NS-HIV lebih rendah dibandingkan pasien HIV tanpa neuropati (3 vs 5,8 /mm2); median IENFD pasien HIV dengan dan tanpa neuropati sensorik lebih rendah dibandingkan kontrol sehat (11,2/mm2). Empat dari lima pasien NS-HIV dengan INEFD rendah mempunyai hitung CD4+ nadir yang rendah. Makrofag CD14+ dapat diidentifikasi perineural pada pasien NS-HIV dan pasien HIV tanpa neuropati sensorik.
Kesimpulan: Prevalensi NS-HIV menurun jauh saat stavudin tidak lagi digunakan. Prevalensi nyeri neuropatik lebih rendah dari prevalensi NS-HIV. Meningkatnya usia dan terdeteksinya viral load berhubungan dengan NS-HIV; PI dan durasi penggunaan ARV yang lebih pendek berhubungan dengan nyeri neuropatik. IENFD pasien HIV lebih rendah dibandingkan kontrol sehat. Pasien NS-HIV dengan IENFD rendah memiliki hitung CD4+ nadir yang rendah. Makrofag CD14+ perineural di epidermis dapat diidentifikasi pada pasien HIV dengan dan tanpa neuropati sensorik.

Introduction: Prevalence of HIV associated sensory neuropathy (HIV-SN) in Cipto Mangunkusumo Hospital (CMH) was 33% in 2006 where all patients used stavudine. Despite stavudine use has been reduced; some patients still complain the symptom of HIV-SN. This study aimed to explore the prevalence and associated factors of HIV-SN and neuropathic pain; to know plasma CCL5 chemokine level and CMV IgG antibody in HIV-SN and neuropathic pain; to study the pattern of intra-epidermal nerve fiber density (IENFD) and perineural CD14+ macrophage in HIV-SN.
Method: It was a cross sectional study carried out at CMH from 2015 until 2017. We tested 197 HIV patients who had antiretroviral treatment (ART) without stavudine for >12 months. The AIDS Clinical Trial Group Brief Peripheral Neuropathy Screening Tool (ACTG-BPNST/BPNST) and Douleur Neuropathique 4 (DN4) questionnaire were used to assess HIV-SN and neuropathic pain respectively. Nerve conduction study (NCS) and Stimulated Skin Wrinkle (SSW) test were performed. The current CD4+ T-cell counts, viral load, CCL5 and IgG CMV antibidoy were measured. Skin biopsy was performed in 5 HIV-SN and 9 HIV-NoSN to assess IENFD and CD14+ macrophage compare to healthy control subjects.
Result: The prevalence of HIV-SN was 14.2% and neuropathic pain was 6.6%. Viral load >500 copies HIV-RNA/ml and increasing age were associated with HIV-SN, while protease inhibitor (PI) and ART duration<2 years were associated with neuropathic pain. CCL5 plasma level and CMV IgG antibody were not associated with HIV-SN and neuropathic pain. IENFDs in HIV-SN were lower than HIV-NoSN (3 vs 5.8/mm2, respectively); IENFDs in HIV patients generally were lower than healthy control (11.2/mm2). Four of 5 HIV-SN patients with low IENFD had low nadir CD4+ T-cell count. CD14+ macrophage can be identified around the nerves of both HIV-SN and HIV-NoSN patients.
Conclusion: Prevalence of HIV-SN in the era without stavudine is lower. Prevalence of neuropathic pain is lower than prevalence of HIV-SN. Increasing age and detectable viral load are associated with HIV-SN; PI and shorter duration of ART are associated with neuropathic pain. IENFDs in HIV patients are lower than healthy control. HIV-SN patients with low IENFD tend to have low nadir CD4+ T-cell count. CD14+ macrophage is present in both HIV patients with and without sensory neuropathy.
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Jakarta: Fakultas Kedokteran Universitas Indonesia, 2018
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UI - Disertasi Membership  Universitas Indonesia Library
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Indria Yogani
"Latar Belakang: HIV adalah infeksi yang menyerang sistem kekebalan tubuh, dengan CD4 sebagai sel targetnya. Dengan ditemukannya Highly Active Antiretroviral Therapy (HAART) diharapkan mampu menurunkan angka morbiditas dan mortalitasnya dengan cara mengurangi replikasi virus HIV dan meningkatkan jumlah CD4. Namun kenaikan CD4 tidak sama untuk setiap pasien. Terdapat faktor lain yang berhubungan dengan kenaikan CD4 pada pasien HIV.
Tujuan: Mengetahui hubungan antara usia, jenis kelamin, indeks massa tubuh, faktor risiko infeksi HIV, jumlah CD4 awal, jumlah infeksi opportunistik, stadium klinis HIV, jenis HAART yang diberikan, kepatuhan minum obat, infeksi tuberkulosis, hepatitis C, infeksi HSV, infeksi CMV, dan obat herbal dengan kenaikan CD4 dalam 6 bulan pertama setelah pemberian HAART.
Metode: Studi kohort retrospektif dilakukan pada pasien HIV rawat jalan di Unit Pelayanan Terpadu HIV RSUPN Cipto Mangunkusumo dalam kurun waktu Januari 2004-Desember 2013. Data penelitian didapatkan dari rekam medis. Hubungan antara usia, indeks massa tubuh, dan jumlah CD4 awal dengan kenaikan CD4 dianalisis dengan uji beda dua rerata menggunakan Uji Mann Whitney. Sedangkan hubungan antara jenis kelamin, faktor risiko infeksi HIV, jumlah infeksi opportunistik, stadium klinis HIV, jenis HAART yang digunakan, kepatuhan minum obat, infeksi tuberkulosis, hepatitis C, infeksi HSV, CMV, dan obat herbal dengan kenaikan CD4 dianalisis dengan uji perbedaan dua kelompok kategorik (Uji Chi Square atau Fisher) serta analisis multivariat dengan teknik regresi logistik.
Hasil: Sebanyak 818 subjek diikutsertakan pada penelitian ini. Sebanyak 368 (45%) subjek tidak mengalami kenaikan CD4 seperti yang diharapkan. Median CD4 awal sebelum terapi 56 sel/mm3 dan setelah 6 bulan terapi 130 sel/mm3. Terdapat hubungan yang bermakna antara jumlah CD4 awal (p<0,001), infeksi tuberkulosis (p=0,010) dan tingkat kepatuhan (p<0,001) dengan kenaikan CD4. Hasil analisis multivariat didapatkan bahwa jumlah CD4 awal (p<0,001; OR: 0,996; IK 95% 0,995-0,998), tidak patuh minum obat (p<0,001; OR:2,907; IK 95%: 2,162-3,909), dan infeksi tuberkulosis (p=0,021; OR: 1,527; IK 95%: 1,065-2,190) berhubungan dengan kenaikan CD4 pada pasien HIV yang mendapat HAART.
Simpulan: Jumlah CD4 awal, kepatuhan minum obat, dan infeksi tuberkulosis mempengaruhi kenaikan CD4 pada pasien HIV yang mendapat Highly Active Antiretroviral Therapy setelah 6 bulan pertama.

Background: HIV infection attacked immune system causing immunodeficiency with CD4 as a targel cell. Highly Active Antiretroviral Therapy given to reduce HIV replications and increased CD4 counts. The increasing of CD4 count is different among each patient. There were several factors associated with the increased of CD4 count after first six months therapy.
Objectives: To prove that age, gender, body mass index, risk factor of HIV infection, CD4 pre HAART, number of opportunistic infections, HIV stadium, type of HAART, adherence, Tuberculosis infection, co-infection Hepatitis C, HSV infection, CMV infection, use of herb associated with the increased of CD4 count.
Methods: Retrospective cohort study conducted in this study, among out patient in Integrated HIV Clinic In Cipto Mangunkusumo General Refferal Hospital between January 2004-December 2013. The data of this study were taken from medical records. For age, body mass index, and CD4 pre HAART associated with the increased of CD4 were analyze using Mann Whitney Test. For variable gender, risk factor for HIV infection, number of opportunistic infections, HIV stadium, type of HAART, adherence, Tuberculosis infection, co-infection of Hepatitis C, HCV infection, CMV infection, and use of herb associated with the increased of CD4 analyze using Chi Square test of Fisher test and for multivariate analysis the logistic regression test.
Results: 818 subjects met the inclusion criteria. 368 subject did not meet the expected CD4 count. The median of CD4 pre HAART was 56 cell/mm3, and after six months therapy was 130 cell/mm3. There was significant correlation between CD4 pre HAART (p<0,001), tuberculosis infection (p=0,010), and adherence with the increasing of CD4 count (p<0,001). From the multivariate analysis, shown that CD4 pre HAART (p<0,001; OR: 0,996; IK 95% 0,995-0,998), not adherence (p<0,001; OR:2,907; IK 95%: 2,162-3,909), and tuberculosis infection (p=0,021; OR: 1,527; IK 95%: 1,065-2,190) associated with the increased of CD4 count after six months therapy.
Conclusion: Adherence, CD4 pre HAART, and Tuberculosis infection were associated with the increasing of CD4 count in HIV patient who received HAART in the first six months therapy.
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Jakarta: Fakultas Kedokteran Universitas Indonesia, 2014
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UI - Tugas Akhir  Universitas Indonesia Library
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Andre Iswara
"ABSTRAK
Gangguan saraf fasialis prefer unilateral merupakan suatu gangguan pada saraf fasialis akibat kelumpuhan otot sebagian atau seluruh wajah. Dalam menangani kasus saraf fasialis perifer unilateral, setiap klinisi dapat menggunakan beberapa modalitas pemeriksaan seperti pemeriksaan motorik sistem Freyss, House-Brackmann, uji topognostik (schirmer, refleks stapedius, gustatometri) dan pemeriksaan elektrofisiologis (kecepatan hantaran saraf, refleks blink, jarum EMG) dalam menentukan derajat kerusakan saraf dan letak lesi berdasarkan onset, derajat kerusakan saraf dan etiologi dalam membantu menegakkan diagnosis dan memperkirakan prognosis. Sangat penting dalam menyampaikan informasi yang tepat dan efektif antar klinisi mengenai keadaan saraf fasialis yang mengalami paresis saraf fasialis dalam menentukan tatalaksana selanjutnya. Penelitian ini menggunakan metode deskriptif cross-sectional dengan pengambilan subjek penelitian secara consecutive sampling di poliklinik Neurotologi THT dan poliklinik EMG Neurologi RSUPN dr. Cipto Mangunkusumo pada bulan Agustus 2012 sampai dengan Mei 2013 dan didapatkan sebanyak 44 subjek penelitian.
Berdasarkan hasil penelitian ini didapatkan hubungan yang bermakna dan kesesuaian yang cukup (Kappa R =0,5, p<0,05) pada 32 subjek penelitian dengan onset lama dengan derajat kerusakan sedang dan berat antara pemeriksaan motorik sistem Freyss, House-Brackmann dengan pemeriksaan elektrofisiologis. Pada penelitian ini tidak didapatkan hubungan yang bermakna dan kesesuaian yang baik (Kappa R=0,011, p=0,935) dalam menentukan letak lesi antara pemeriksaan uji topognostik dengan pemeriksaan elektrofisiologis. Tiga belas subjek penelitian tidak dapat ditentukan letak lesi berdasarkan pemeriksaan elektrofisiologis pada onset kronis dengan derajat kerusakan sedang dan berat sedangkan pemeriksaan uji topognostik mampu menentukan letak lesi pada onset akut maupun kronis. Untuk daerah-daerah yang tidak memiliki modalitas pemeriksaan elektrofisiologis, pemeriksaan motorik sistem Freyss dan House-Brackmann dapat digunakan dalam menegakkan diagnosis dan memprediksi prognosis.

ABSTRACT
Unilateral peripheral facial nerve palsy is a disturbance in facial nerve caused by partial or complete muscle paralysis. Clinician can use multiple examination modality such as Freyss system, House-Brackmann, topognostic test (schirmer, stapedius reflex, gustatometry) and electrophysiology (nerve conduction velocity, blink reflex, EMG needle) to establish diagnosis and prognosis. It is very important to deliver right and effective information between clinician about facial nerve condition and paralysis to determine further management. Achieve conformity between Freyss system, House-Brackmann, topognostic study and electophysiologic examination in diagnosis and prognosis. This study used descriptive cross-sectional method by taking study subject with consecutive sampling in Neurotology division of ENT department and EMG division of Neurology Department outpatient-clinic and 44 study subjects.
According to study result, there is significance and conformity (Kappa R =0,5, p=0,005) for 32 subjects late onset with detriment degree moderate severe between motoric examination Freyss, House-Brackmann and electrophysiologic examination. In this study there is no significanceand conformity (Kappa R=0,011, p=0,935) between determining lesion site between topognostic test and electrophysiology examination. Thirteen study subjects could not be determined for lesion site, due to chronic onset with moderate severe damage by electrophysiology examination, whereas topognostic test can determine lesion site in acute nor chronic onset. In region without facility for electrophysiologic examination, Freyss and House-Brackmann motoric system can be used in establishing diagnosis and determining prognosis."
Jakarta: Fakultas Kedokteran Universitas Indonesia, 2013
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UI - Tesis Membership  Universitas Indonesia Library
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Wulunggono
"Latar Belakang. Walaupun pasien HIV mendapat terapi antiretroviral yang efektif, penurunan fungsi fisik sering ditemukan lebih awal dan menimbulkan masalah baru berupa penuaan dan frailty.
Tujuan. Mengetahui proporsi dan faktor-faktor yang berhubungan dengan prefrail dan frail pada pasien HIV dalam terapi antiretroviral.
Metode. Desain studi potong lintang pada pasien HIV usia ≥30 tahun dalam terapi ARV minimal 6 bulan. Pasien yang memenuhi inklusi dilakukan pencatatan demografis, penyakit komorbid, faktor terkait HIV seperti lama terdiagnosis, lama ARV, dan CD4, pengukuran antropometri seperti indeks massa tubuh, penilaian depresi dengan Indo BDI-II, dan penilaian frailty dengan kriteria Fried. Pasien dengan riwayat infeksi otak, kanker, dan oportunistik aktif dieksklusi. Analisis bivariat dan multivariat dilakukan pada faktor-faktor tersebut.
Hasil. Terdapat 164 pasien yang dianalisis. Proporsi prefrail sebanyak 51,2% (84 pasien) dan frail 3,7% (6 pasien), dengan komponen dominan pada kelemahan genggam. Pasien laki-laki sebanyak 72% dengan median usia (IQR) 40,5 (36-47) tahun, dan median CD4 nadir (IQR) 53 (21-147) sel/mm3, median CD4 awal (IQR) 77 (32 - 206) sel/mm3. Hepatitis C menjadi faktor komorbid terbanyak. Depresi berhubungan dengan prefrail dan frail dengan OR 2,14 (IK95%: 1,034-4,439) dan p = 0,036. Tidak terdapat hubungan faktor usia ≥50 tahun, ≥2 penyakit komorbid, lama terdiagnosis HIV ≥5 tahun, lama ARV ≥5 tahun, CD4 <200 sel/mm3, indeks massa tubuh ≥25 kg/m2, dan pendapatan rendah dengan prefrail dan frail.
Kesimpulan. Terdapat proporsi prefrail sebanyak 51,2% dan frail 3,7%. Depresi merupakan salah satu faktor yang terbukti berhubungan terhadap prefrail dan frail pada pasien HIV dalam terapi ARV.

Background. Although HIV patients receive effective antiretroviral therapy, decrease in physical function is often found earlier and creates new problems in the form of aging and frailty
Aim. to determine the proportion and factors associated with prefrail and frail in HIV patients on antiretroviral therapy.
Method. A cross-sectional study design in HIV patients aged ≥30 years who were on ARV therapy for at least 6 months. Patients who fulfilled the inclusion were recorded demographically, comorbid diseases, HIV-related factors such as length of diagnosis, duration of ARV, CD4, anthropometric measurements such as body mass index, depression assessment with Indo BDI-II, and frailty assessment with Fried criteria. Patients with a history of brain infection, cancer, and active opportunists were excluded. Bivariate and multivariate analysis was carried out on these factors.
Results. There were 164 patients analyzed. The proportions of prefrail and frail were 51.2% and 3.7% respectively, with the dominant component in muscle weakness. Male patients were 72% with median age (IQR) 40.5 (36-47) years, median baseline CD4 (IQR) 77 (32 - 206) cell/mm3, and median nadir CD4 (IQR) 53 (21-147) cells/mm3. Hepatitis C is the most comorbid factor. Depression is related to prefrail and frail with OR 2.14 (95%CI: 1,034-4,439) and p = 0,036. There was no correlation between factors such as age ≥50 years, ≥2 comorbid diseases, length of diagnosis of HIV ≥5 years, duration of ARV ≥5 years, CD4 cell count <200 cells/mm3, body mass index ≥25 kg/m2, and low income with prefrail and frail.
Conclusion. The proportions of prefrail and frail are 51.2% and 3.7% respectively. Depression is one of the factors that is proven to be related to prefrail and frail in HIV patients in ARV therapy.
"
Jakarta: Fakultas Kedokteran Universitas Indonesia, 2019
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Rizki Febriani Putri
"Latar Belakang Walaupun mendapatkan terapi antiretroviral (ARV), inflamasi kronik akibat infeksi HIV dikombinasikan dengan faktor-faktor lain menyebabkan proses penuaan lebih dini pada pasien HIV/AIDS, salah satu tandanya risiko jatuh.
Tujuan Mengetahui proporsi kejadian jatuh dan risiko jatuh serta faktor faktor yang berhubungan pada pasien HIV/AIDS dalam terapi ARV.
Metode Studi potong lintang dilakukan pada pasien HIV/AIDS berusia > 40 tahun dalam terapi ARV minimal 6 bulan. Pada pasien yang memenuhi kriteria inklusi dilakukan pencatatan data demografis, pengukuran antropometri, faktor terkait HIV, terapi ARV, komorbid, obat, penilaian depresi dengan Indo-BDI-II, neuropati dengan kriteria Toronto, frailty dengan kriteria Fried, dan risiko jatuh dengan uji Timed Up and Go (TUG). Pasien menolak, tidak dapat berjalan dan memiliki gangguan motorik dieksklusi. Analisis bivariat dan multivariat dilakukan pada faktor-faktor tersebut.
Hasil Dari 102 sampel didapatkan proporsi kejadian jatuh 24,5% dan risiko jatuh sebesar 51,96%. Subjek mayoritas laki-laki (83,3%), median usia (IQR) 45 (5) tahun, CD4 nadir median (IQR) 71,5 (220,25) sel/mm3, CD4 saat ini median (IQR) 495,5 (361) sel/mm3, komorbid terbanyak hepatitis C (31,3%), polifarmasi 21,6% subjek, dalam terapi lini 2 ARV (10.78%), depresi (14,71%), neuropati 38,2%) prefrail 53,9% dan frail 14,7%, penapisan demensia 14,7%. Faktor yang berhubungan dengan risiko jatuh adalah prefrail/frail (OR 6,395, IK95% 2,348-17,417 p<0,001) riwayat jatuh (OR 3,162 IK95% 1,085-9,212 p 0,035) dan penggunaan Efavirenz (OR 5,878 IK95% 1,083-31,906 p 0,040).
Kesimpulan Proporsi kejadian jatuh pada pasien HIV/AIDS dalam terapi ARV meyerupai populasi geriatri non HIV dengan risiko jatuh 52%. Faktor yang behubungan adalah status prefrail/frail, riwayat jatuh sebelumnya, dan penggunaan Efavire

Background Despite given Antiretroviral Therapy (ART), chronic inflammation due to HIV infection combined with other factors implicate in the early aging process. Fall risk is one of the aging symptoms that can be assessed objectively.
Aims To determine proportion of any fall and factors associated with risk of fall in PLWH undergoing antiretroviral therapy.
Methods cross sectional study in PLWH aged 40 years or older who has take ART at least for 6 months. Data were recorded in subjects fulfilled inclusion criteria, including demographic data, anthropometry measurements, HIV related factors, comorbidities, drugs prescribed, depression using Indo-BDI-II questionnaire, neuropathy assesment sing Toronto Scoring criteria, Fried criteria frailty, and fall risk assessed by Timed Up and Go Test. Patients denied to participate, unable to walk, or having motoric abnormality in upper extremity was excluded. Bivariat and multivariat analysis was carried out to these factors.
Results among 102 subjects, proportions of any falls was 24,5% subjects and proportions of fall risk was 52%. Most of subjects were male (83,3%), median of age (IQR) was 45 (5) years, with nadir CD4 (IQR) was 71,5 (220,25) cell/mm3 and current CD4 was 495,5 (361) cells/mm3. Hepatitis C was the most comorbid disease (31,3%), polypharmacy prescribed in 21,6%, and 10,8% were in LPV/r therapy. Factors included were depression found in 14,7%, neuropathy in 38,2%m prefrail 53,9%, frail 14,7%, and patients positive screened for dementia 14,7%. Significant factors associated with risk of fall were prefrail/frail status (OR 6,395, IK95% 2,348-17,417 p<0,001), history of fall (OR 3,162 IK95% 1,085-9,212 p 0,035), and under EFV prescription (OR 5,878 IK95% 1,083-31,906 p 0,040).
Conclusion proportion of any fall in PLWH undergoing antiretroviral therapy resembled those in geriatric population, with high rate of fall risk up to 52% of the patients. Factors associated with risk of fall were frail/prefrail status, history of previous fall, and current EFV use.
"
Jakarta: Fakultas Kedokteran Universitas Indonesia, 2020
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UI - Tugas Akhir  Universitas Indonesia Library
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Rahajeng Dewantari
"Ketaatan minum obat dalam penanganan HIV/AIDS dengan pengobatan ARV merupakan faktor yang penting dalam menentukan keberhasilan terapi. Di Indonesia belum ada data yang menyebutkan angka pasti ketaatan minum obat ARV pada ODHA. Ketaatan minum obat ARV dipengaruhi oleh adanya faktorfaktor psikologis (stigma diri dan fungsi kognitif) dan non psikologis yang terdiri dari faktor demografi (umur, waktu tempuh tempat tinggal ke rumah sakit, akses berobat, tingkat pendidikan, pekerjaan, tinggal sendiri atau bersama orang lain, pembiayaan berobat, penggunaan NAPZA) dan faktor obat dan penyakit (kompleksitas regimen obat, adanya infeksi oportunistik, sumber transmisi HIV).
Hasil penelitian ini menunjukkan bahwa prevalensi ketaatan minum obat ARV pada ODHA yang berobat di UPT HIV RSUPN Cipto Mangunkusumo adalah 67,7%, stigma diri memiliki hubungan yang bermakna dengan ketaatan minum obat ARV, sedangkan faktor non psikologis yang diteliti dan fungsi kognitif tidak memiliki hubungan yang bermakna dengan ketaatan minum obat ARV.

Adherence to ARV is an important factor in determining the success of HIV/AIDS treatment. There has been no data about adherence to ARV in plwh in indonesia. Adherence to ARV is influenced by psychological factors (self-stigma and cognitive function) and non-psychological factors consisting of demographic (age, travel time between living place and hospital, access to treatment, level of education, occupation, living alone or with others, treatment payment, illicit drugs use), disease and treatment factor (treatment regimen complexity, opportunistic infections, source of HIV transmission).
The result of this study showed that prevalence of adherence to ARV in plwh coming to HIV integrated service unit Cipto Mangunkusumo hospital is 67,7%, that self-stigma had significant relation with adherence to ARV, while psychological factors and cognitive function had no significant relation with adherence to ARV.
"
Depok: Fakultas Kedokteran Universitas Indonesia, 2014
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UI - Tesis Membership  Universitas Indonesia Library
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Farid Kurniawan
"[ABSTRAK
Latar Belakang: Terapi antiretroviral (ARV) terbukti secara efektif dapat menekan replikasi HIV. Pengukuran viral load (VL) merupakan prediktor yang lebih baik dibanding kriteria klinis atau imunologis untuk menilai kegagalan atau keberhasilan terapi ARV. Karena keterbatasan sumber daya, maka pemeriksaan VL tidak selalu mudah untuk diakses oleh pasien HIV yang mendapat terapi ARV sehingga perlu untuk diketahui faktor-faktor pada pasien yang dapat memprediksi terjadinya kegagalan virologis.
Tujuan: Mengetahui faktor prediktor kegagalan virologis pada pasien HIV yang mendapat terapi ARV lini pertama sesuai paduan ARV terbaru di Indonesia.
Metode: Penelitian ini merupakan studi kohort retrospektif pada pasien HIV rawat jalan dewasa di RSCM yang mulai terapi ARV lini pertama selama periode Januari 2011-Juni 2014. Pasien HIV yang mempunyai data VL 6-9 bulan setelah mulai terapi ARV dengan kepatuhan berobat baik dimasukkan sebagai subjek penelitian. Kegagalan virologis dinyatakan sebagai nilai VL ≥ 400 kopi/mL setelah minimal 6 bulan terapi ARV dengan kepatuhan berobat baik. Paduan ARV yang digunakan terdiri dari dua NNRTI (salah satu dari TDF/AZT/d4T ditambah 3TC) dengan satu NNRTI (NVP atau EFV). Usia, faktor risiko penularan HIV, stadium klinis HIV menurut WHO, ko-infeksi TB, indeks massa tubuh, kadar hemoglobin, dan jumlah CD4 awal terapi serta basis paduan terapi ARV merupakan variabel yang diteliti pada penelitian ini.
Hasil: Terdapat 197 pasien sebagai subjek penelitian ini. Kegagalan virologis didapatkan pada 21 pasien (10,7%). Semua variabel yang diteliti belum terbukti dapat memprediksi kegagalan virologis pada pasien HIV yang mendapat terapi ARV lini pertama dengan adherens baik. Terdapat peningkatan risiko kegagalan virologis pada pasien dengan usia yang lebih muda, faktor risiko penasun, stadium klinis lanjut, adanya ko-infeksi TB, dan paduan ARV TDF+3TC+NVP tetapi tidak bermakna secara statistik.!!
Simpulan: Dari variabel yang diteliti, tidak didapatkan variabel yang terbukti sebagai prediktor awal kegagalan virologis pada pasien HIV yang mendapat terapi ARV lini pertama dengan adherens baik.

ABSTRACT
Background: Antiretroviral therapy (ART) effectively suppress HIV replication. Viral load (VL) measurement is better predictor than clinical or immunological criteria to evaluate failure or success of ART. However, in the country with limited resources, VL measurement is not easily accessible by HIV patients receiving ARV therapy therefore it is necessary to know which factors in the patients that can predict virological failure.
Objectives: To know early predictive factor of virological failure in HIV patients receiving recent first line ARV therapy regimen in Indonesia
Methods: This study was a retrospective cohort study among adult HIV patients in Out-patient Clinic of Cipto Mangunkusumo General Hospital that started ARV therapy during periode January 2011-June 2014. HIV patients with good adherence that have VL data 6-9 months after initiation of ARV therapy were included in this study. Virological failure was defined as VL ≥ 400 copies/mL after minimum of 6 months therapy with good adherence. ARV regimen used in this study consist of two NRTI (one of TDF/AZT/d4T plus 3TC) combined with one NNRTI (NVP or EFV). Age, risk factor for HIV infection, HIV clinical stage, HIV- TB co-infection, baseline CD4 value, hemoglobin level, body mass index, and ARV therapy regimen at the time of initiation were among the variables that analyzed in this study.
Results: There are 197 patients as subjects in this study. Virological failure was found in 21 patients (10,7%). All the variables included in this study can not predict virological failure in HIV patients receiving first line ART with good adherence. There is increase risk of virological failure in patients with younger age, IDU as risk factor for HIV infection, late clinical stage, TB co-infection, and ARV regimen TDF+3TC+NVP but not reaching statistically significant.
Conclusion: There is no variable in this study proved to be early predictive factor for virological failure in HIV patients receiving first line ART with good adherence.;Background: Antiretroviral therapy (ART) effectively suppress HIV replication. Viral load (VL) measurement is better predictor than clinical or immunological criteria to evaluate failure or success of ART. However, in the country with limited resources, VL measurement is not easily accessible by HIV patients receiving ARV therapy therefore it is necessary to know which factors in the patients that can predict virological failure.
Objectives: To know early predictive factor of virological failure in HIV patients receiving recent first line ARV therapy regimen in Indonesia
Methods: This study was a retrospective cohort study among adult HIV patients in Out-patient Clinic of Cipto Mangunkusumo General Hospital that started ARV therapy during periode January 2011-June 2014. HIV patients with good adherence that have VL data 6-9 months after initiation of ARV therapy were included in this study. Virological failure was defined as VL ≥ 400 copies/mL after minimum of 6 months therapy with good adherence. ARV regimen used in this study consist of two NRTI (one of TDF/AZT/d4T plus 3TC) combined with one NNRTI (NVP or EFV). Age, risk factor for HIV infection, HIV clinical stage, HIV- TB co-infection, baseline CD4 value, hemoglobin level, body mass index, and ARV therapy regimen at the time of initiation were among the variables that analyzed in this study.
Results: There are 197 patients as subjects in this study. Virological failure was found in 21 patients (10,7%). All the variables included in this study can not predict virological failure in HIV patients receiving first line ART with good adherence. There is increase risk of virological failure in patients with younger age, IDU as risk factor for HIV infection, late clinical stage, TB co-infection, and ARV regimen TDF+3TC+NVP but not reaching statistically significant.
Conclusion: There is no variable in this study proved to be early predictive factor for virological failure in HIV patients receiving first line ART with good adherence., Background: Antiretroviral therapy (ART) effectively suppress HIV replication. Viral load (VL) measurement is better predictor than clinical or immunological criteria to evaluate failure or success of ART. However, in the country with limited resources, VL measurement is not easily accessible by HIV patients receiving ARV therapy therefore it is necessary to know which factors in the patients that can predict virological failure.
Objectives: To know early predictive factor of virological failure in HIV patients receiving recent first line ARV therapy regimen in Indonesia
Methods: This study was a retrospective cohort study among adult HIV patients in Out-patient Clinic of Cipto Mangunkusumo General Hospital that started ARV therapy during periode January 2011-June 2014. HIV patients with good adherence that have VL data 6-9 months after initiation of ARV therapy were included in this study. Virological failure was defined as VL ≥ 400 copies/mL after minimum of 6 months therapy with good adherence. ARV regimen used in this study consist of two NRTI (one of TDF/AZT/d4T plus 3TC) combined with one NNRTI (NVP or EFV). Age, risk factor for HIV infection, HIV clinical stage, HIV- TB co-infection, baseline CD4 value, hemoglobin level, body mass index, and ARV therapy regimen at the time of initiation were among the variables that analyzed in this study.
Results: There are 197 patients as subjects in this study. Virological failure was found in 21 patients (10,7%). All the variables included in this study can not predict virological failure in HIV patients receiving first line ART with good adherence. There is increase risk of virological failure in patients with younger age, IDU as risk factor for HIV infection, late clinical stage, TB co-infection, and ARV regimen TDF+3TC+NVP but not reaching statistically significant.
Conclusion: There is no variable in this study proved to be early predictive factor for virological failure in HIV patients receiving first line ART with good adherence.]"
2015
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UI - Tesis Membership  Universitas Indonesia Library
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Suzy Maria
"ABSTRAK
Latar Belakang: Hingga saat ini belum ada panduan mengenai paduan terapi
antiretroviral (antiretroviral therapy/ART) terpilih pada pasien HIV dewasa
dengan riwayat interupsi tidak terencana. Kondisi pasien pada saat reintroduksi
ART perlu dievaluasi sebagai dasar pemilihan paduan ART
Tujuan: Mengetahui proporsi keberhasilan virologis pada reintroduksi ART lini
pertama pasca interupsi tidak terencana. Mengetahui hubungan antara berbagai
faktor klinis dan laboratoris dengan keberhasilan virologis pada reintroduksi
tersebut.
Metode: Penelitian kohort retrospektif dilakukan pada pasien HIV yang
mendapatkan reintroduksi ART lini pertama pasca interupsi tidak terencana
selama minimal 1 bulan. Data didapatkan dari rekam medis RS dr. Cipto
Mangunkusumo di Jakarta. Viral load (VL) dinilai 6-18 bulan setelah reintroduksi
ART lini pertama, dinyatakan berhasil bila VL <400 kopi/ml. Dilakukan analisis
terhadap faktor yang berhubungan dengan keberhasilan virologis tersebut.
Hasil: Selama periode Januari 2005 s.d. Desember 2014 terdapat 100 subjek yang
mendapatkan reintroduksi ART lini pertama dan memiliki data viral load 6-18
bulan pasca reintroduksi. Pasca reintroduksi ART didapatkan keberhasilan
virologis pada 55 (55%) subjek. Pada analisis didapatkan dua faktor yang
berhubungan dengan keberhasilan virologis pada reintroduksi ART lini pertama,
yaitu frekuensi interupsi satu kali (adjusted OR/aOR 5,51; IK95% 1,82-16,68;
p=0,003), nilai CD4 saat reintroduksi ≥200 sel/mm
xi
3
(aOR 4,33; IK95% 1,1416,39,
p=0,031).
Simpulan:
Proporsi keberhasilan virologis pada reintroduksi ART lini pertama
pasca interupsi tidak terencana adalah 55%. Pasien dengan frekuensi interupsi 1
kali dan pasien dengan nilai CD4 saat reintroduksi ≥200 sel/mm
3
memiliki kecenderungan untuk mencapai keberhasilan virologis pada reintroduksi ART.
ABSTRACT
There is no guideline concerning antiretroviral therapy (ART) of
choice for adult HIV patients after unplanned interruption. Hence, patients?
conditions at time of ART reintroduction need to be evaluated as a basis for
selecting ART regiment.
Objectives: To know the proportion of virological success of first line ART
reintroduction after unplanned interruption. To know the association between
either clinical or laboratory factors and virological success in reintroduction.
Methods: We conducted a retrospective cohort study in HIV patients that were
reintroduced to first line ART after having unplanned interruption for at least one
month period. The data were collected from medical records of Dr. Cipto
Mangunkusumo Hospital in Jakarta. Viral load (VL) was evaluated at 6-18
months after first line ART reintroduction, declared as a success if VL <400
copies/mL. Analysis was done to factors associated with such virological success.
Results: Between January 2005 and December 2014, 100 subjects were
reintroduced to first line ART and having VL data in 6 to 18 months after the
reintroduction. Virological success was achieved in 55 (55%) subjects. In the
analysis we found that virological success was associated with interrupted once
(adjusted OR/aOR 5.51%, 95%CI 1.82-16.68, p=0.003) and CD4 ≥200 cell/mm
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3
at the time of reintroduction (aOR 4.33, 95%CI 1.14-16.39, p=0.031).
Conclusions: Proportion of virological success on first line ART reintroduction
after unplanned interruption was 55%. Patients who were having interrupted once
and patients with CD4 ≥200 cell/mm
3
at the time of reintroduction would have
higher odds of virological success on first line ART reintroduction.
;Background: There is no guideline concerning antiretroviral therapy (ART) of
choice for adult HIV patients after unplanned interruption. Hence, patients?
conditions at time of ART reintroduction need to be evaluated as a basis for
selecting ART regiment.
Objectives: To know the proportion of virological success of first line ART
reintroduction after unplanned interruption. To know the association between
either clinical or laboratory factors and virological success in reintroduction.
Methods: We conducted a retrospective cohort study in HIV patients that were
reintroduced to first line ART after having unplanned interruption for at least one
month period. The data were collected from medical records of Dr. Cipto
Mangunkusumo Hospital in Jakarta. Viral load (VL) was evaluated at 6-18
months after first line ART reintroduction, declared as a success if VL <400
copies/mL. Analysis was done to factors associated with such virological success.
Results: Between January 2005 and December 2014, 100 subjects were
reintroduced to first line ART and having VL data in 6 to 18 months after the
reintroduction. Virological success was achieved in 55 (55%) subjects. In the
analysis we found that virological success was associated with interrupted once
(adjusted OR/aOR 5.51%, 95%CI 1.82-16.68, p=0.003) and CD4 ≥200 cell/mm
xii
Universitas Indonesia
3
at the time of reintroduction (aOR 4.33, 95%CI 1.14-16.39, p=0.031).
Conclusions: Proportion of virological success on first line ART reintroduction
after unplanned interruption was 55%. Patients who were having interrupted once
and patients with CD4 ≥200 cell/mm
3
at the time of reintroduction would have
higher odds of virological success on first line ART reintroduction.
;Background: There is no guideline concerning antiretroviral therapy (ART) of
choice for adult HIV patients after unplanned interruption. Hence, patients?
conditions at time of ART reintroduction need to be evaluated as a basis for
selecting ART regiment.
Objectives: To know the proportion of virological success of first line ART
reintroduction after unplanned interruption. To know the association between
either clinical or laboratory factors and virological success in reintroduction.
Methods: We conducted a retrospective cohort study in HIV patients that were
reintroduced to first line ART after having unplanned interruption for at least one
month period. The data were collected from medical records of Dr. Cipto
Mangunkusumo Hospital in Jakarta. Viral load (VL) was evaluated at 6-18
months after first line ART reintroduction, declared as a success if VL <400
copies/mL. Analysis was done to factors associated with such virological success.
Results: Between January 2005 and December 2014, 100 subjects were
reintroduced to first line ART and having VL data in 6 to 18 months after the
reintroduction. Virological success was achieved in 55 (55%) subjects. In the
analysis we found that virological success was associated with interrupted once
(adjusted OR/aOR 5.51%, 95%CI 1.82-16.68, p=0.003) and CD4 ≥200 cell/mm
xii
Universitas Indonesia
3
at the time of reintroduction (aOR 4.33, 95%CI 1.14-16.39, p=0.031).
Conclusions: Proportion of virological success on first line ART reintroduction
after unplanned interruption was 55%. Patients who were having interrupted once
and patients with CD4 ≥200 cell/mm
3
at the time of reintroduction would have
higher odds of virological success on first line ART reintroduction.
;Background: There is no guideline concerning antiretroviral therapy (ART) of
choice for adult HIV patients after unplanned interruption. Hence, patients?
conditions at time of ART reintroduction need to be evaluated as a basis for
selecting ART regiment.
Objectives: To know the proportion of virological success of first line ART
reintroduction after unplanned interruption. To know the association between
either clinical or laboratory factors and virological success in reintroduction.
Methods: We conducted a retrospective cohort study in HIV patients that were
reintroduced to first line ART after having unplanned interruption for at least one
month period. The data were collected from medical records of Dr. Cipto
Mangunkusumo Hospital in Jakarta. Viral load (VL) was evaluated at 6-18
months after first line ART reintroduction, declared as a success if VL <400
copies/mL. Analysis was done to factors associated with such virological success.
Results: Between January 2005 and December 2014, 100 subjects were
reintroduced to first line ART and having VL data in 6 to 18 months after the
reintroduction. Virological success was achieved in 55 (55%) subjects. In the
analysis we found that virological success was associated with interrupted once
(adjusted OR/aOR 5.51%, 95%CI 1.82-16.68, p=0.003) and CD4 ≥200 cell/mm
xii
Universitas Indonesia
3
at the time of reintroduction (aOR 4.33, 95%CI 1.14-16.39, p=0.031).
Conclusions: Proportion of virological success on first line ART reintroduction
after unplanned interruption was 55%. Patients who were having interrupted once
and patients with CD4 ≥200 cell/mm
3
at the time of reintroduction would have
higher odds of virological success on first line ART reintroduction.
"
Fakultas Kedokteran Universitas Indonesia, 2015
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UI - Tugas Akhir  Universitas Indonesia Library
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