2018
DOI: 10.1111/apt.14497
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Review article: long‐term safety of oral anti‐viral treatment for chronic hepatitis B

Abstract: SummaryBackgroundSafety profile of nucleos(t)ide analogues is an important issue in view of its widespread use for decades in patients with chronic hepatitis B (CHB).AimTo review and evaluate the latest evidence on the safety profiles of the six approved nucleoside analogues.MethodsRelevant articles related to nucleoside analogue safety were selected for review following extensive language‐ and date‐unrestricted, electronic searches of the literature.ResultsNephrotoxicity has been well reported in patients rec… Show more

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Cited by 73 publications
(59 citation statements)
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References 55 publications
(60 reference statements)
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“…Both TDF and adefovir dipivoxil are nucleotide analogues and excreted via kidney by glomerular filtration. Mechanisms of nucleoside analogue induced renal toxicity include renal tubular injury and mitochondrial toxicity . However, the data concerning nephrotoxicity of TDF have been debatable in patients with CHB.…”
Section: Discussionmentioning
confidence: 99%
“…Both TDF and adefovir dipivoxil are nucleotide analogues and excreted via kidney by glomerular filtration. Mechanisms of nucleoside analogue induced renal toxicity include renal tubular injury and mitochondrial toxicity . However, the data concerning nephrotoxicity of TDF have been debatable in patients with CHB.…”
Section: Discussionmentioning
confidence: 99%
“…In addition, data on antiviral treatment in HBV/HCV+ mothers were unavailable, although usually, most parturients do not require therapy. Moreover, antiviral therapies used in HBV/HCV+ mothers during pregnancy are listed as category B or C under the FDA pregnancy categories, so it seems unlikely that maternal antiviral treatment accounts for our findings. We suggest that future studies will include data on antiviral treatments and investigate possible mechanisms of this study findings, as well.…”
Section: Discussionmentioning
confidence: 99%
“…13 Beberapa mekanisme telah ditemukan untuk menjelaskan bagaimana penurunan fungsi ginjal ini terjadi pada (2) penurunan volume arterial efektif pada penyakit hati kronik tahap akhir dan sirosis, yang menimbulkan hipoperfusi ginjal dan penurunan fungsi ginjal 15 ; dan (3) efek nefrotoksisitas jangka panjang dari analog nukleos(t) ida. 16 Observasi pada kelompok tenofovir di minggu ke-48 menunjukkan rerata kreatinin serum meningkat secara signifikan dari 0,88 (SB 0,17) mg/dL pada awal terapi menjadi 0,94 (SB 0,26) mg/dL (p = 0,008) pada minggu ke-48 dan rerata eLFG juga menurun secara signifikan, yaitu dari 93,69 (SB 16,56) mL/menit/1,73 m 2 menjadi 90,67 (SB 20,89) mL/menit/1,73 m 2 dalam 48 minggu (p = 0,029) pada pasien infeksi hepatitis B kronik dengan eLFG ≥60 mL/menit/1,73 m 2 .…”
Section: Diskusiunclassified
“…Mekanisme tenofovir yang berhubungan dengan nefrotoksisitas yaitu akumulasi intraseluler dari tenofovir menyebabkan saturasi MRP-4 sehingga menimbulkan kerusakan tubulus ginjal. 16 Sebuah penelitian di Taiwan membandingkan keamanan ginjal pada pemberian telbivudin dan tenovofir terhadap pasien infeksi hepatitis B kronik tanpa gangguan ginjal sebelumnya (eLFG ≥60 mL/menit/1,73 m 2 ). Estimasi LFG menurun secara signifikan pada kelompok tenovofir dalam 2 tahun pertama yang dibandingkan dengan awal.…”
Section: Diskusiunclassified