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Hasil Pencarian

Ditemukan 11 dokumen yang sesuai dengan query
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Sudardjat Sugiri
"Kebutaan, penurunan fungsi penglihatan dan kesakitan mata telah dinyatakan sebagai masalah kesehatan masyarakat yang penting di wilayah Asia Tenggara (WHO). Berdasarkan WHO maka diperkirakan terdapat 12 juta kebutaan dan 60 juta penurunan penglihatan di Asia Tenggara. Di Indonesia sendiri berdasarkan survai morbiditas mata dan kebutaan tahun 1982 yang dikelola oleh Direktorat Jendral Pembinaan Kesehatan Masyarakat Departemen Kesehatan RI menyatakan bahwa prevalensi kebutaan di Indonesia berkisar 1,2% dari jumlah penduduk Indonesia. Dari angka tersebut prosentase penyebab kebutaan utama ialah :
- katarak 0.70%
- kelainan kornea 0.13%
- penyakit glaukoma 0.10%
- kelainan refraksi 0.06%
- kelainan retina 0.03%
- kelainan nutrisi 0.02%
Banyak macam cara pengobatan penyakit glaukoma baik secara obat-obatan maupun secara operasi. Cara operasi bisa dilakukan dengan membuka aliran akuos dari bilik mata depan ke celah sub konjungtiva pada mata taripa blok pupil, untuk membentuk pengaliran cairan akuos, atau dengan mengurangi pembentukan cairan akuos di badan siliar(3,4,5).
Dari pengalaman klinis dapat terjadi suatu keadaan glaukoma yang berat misalnya glaukoma refrakter atau glaukoma absolut, glaukoma hemaragik atau glaukoma neovaskular, dimana tindakan operasi kurang berhasil. Pada keadaan diatas perlu dipikirkan cara pengobatan yang lebih efektif lain untuk menurunkan tekanan intra okular. Di Rumah Sakit Dr.Cipto Mangunkusumo, pada glaukoma neovaskular dilakukan tindakan transkleral kriokoagulasi dan transkleral diatermi dengan tujuan mengurangi keadaan iskemia retina/koroid, untuk menurunkan tekanan intra okular.
Sikatrik korioretina terjadi karena kerusakan epitel pigmen retina dan reseptor retina, terjadi penggabungan dari lapisan retina luar ke membrana Bruch, terjadi perubahan jaringan ikat korio-kapiler dan lapisan pembuluh darah koroid dalam, degenerasi dan disorganisasi dari retina sensoris dan sel-sel penyokong (6,8). Keadaan ini dapat terjadi akibat perubahan atau setelah tindakan krioterapi atau diatermi dari pada retina, baik pada perubahan penyakit retina maupun pada terapi glaukoma diatas.
Pada suatu kelainan di retina , dapat di ikuti dengan penurunan tekanan intra okular (T.I.O.) yang moderat, pengurangan aliran humor akuos melalui bilik mata depan, suar ringan di akuos dan peningkatan kadar protein cairan subretinal. Ada 2 hipotesa kemungkinan terjadinya keadaan tersebut. Hipotesa pertama menyatakan bahwa kelainan retina akan menimbulkan inflamasi ringan sistem traktus uvea, disebabkan kegagalan sawar darah-akuos, disertai suar akuos & pengurangan produksi akuos, mengakibatkan peninggian protein cairan sub retinal. Hipotesa kedua mengatakan bahwa terjadi kegagalan ringan sawar darah akuos. Dan juga, produksi akuos tetap normal tetapi terjadi perubahan aliran dari bilik mata belakang kerongga badan kaca, melalui kelainan diretina dan melewati epitel pigmen retina.
Aliran yang tidak lazim ini (misdirected/unconvention al route) dari humor akuos menyebabkan penurunan tekanan intra okular, dan membawa protein dari bilik mata belakang yang akan mengumpui di celah subretinal.
Pembuktian adanya aliran cairan dari badan kaca ke celah retina ini terlihat pada percobaan binatang kera yang disuntikan cairan fluoresin iso tiosianat dextran. Disini terjadi kerusakan intregitas retina sensoris, yang diikuti pengaliran cairan badan kaca ke celah subretinal dan akan di absorpsi pembuluh darah koroid dan menimbulkan penurunan tekanan intra okular."
Fakultas Kedokteran Universitas Indonesia, 1990
T58520
UI - Tesis Membership  Universitas Indonesia Library
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Mariati S. Muchlis
"ABSTRAK
Sayatan pada operasi katarak biasanya menyebabkan beberapa tingkat pendataran meridian kornea pada "right angle" ke arah sayatan tersebut. Dengan sayatan di bagian superior berarti adanya pendataran pada meridian vertikal.
Perjalanan yang lambat dan progresif dari penyembuhan luka operasi menyebabkan regangan jaringan parut sehingga terjadi pendataran dari bagian atas kornea yang menghasilkan astigmatisme "Againts the rule".
Dikatakan bahwa astigmatisme yang terjadi segera setelah operasi disebabkan oleh karena jahitan yang terlalu kencang dan akan berkurang selama periode pasca bedah ( 9 ).
Sing (7) berpendapat bahwa astigmatisme yang terjadi segera setelah operasi lebih tinggi dibandingkan pasca pembedahan setelah 6 minggu di mana akan menurun hampir separuhnya.
Yaffe (10) menganjurkan pemberian kaca mata afakia segera setelah hasil keratometer dan refraksi stabil, biasanya pada minggu ke-6 sampai minggu ke-8 pasca bedah.
Dia malah memberikan kaca mata afakia setelah 4 minggu dan kadang-kadang setelah 8 minggu, hal ini tergantung dari tehnik pembedahan.
Menetapnya hasil keratometer atau refraksi selain tergantung dari teknik pembedahan, juga dipengaruhi oleh proses penyembuhan luka yang bervariasi secara individual, di samping itu berbagai faktor lain seperti operator, benang yang dipakai, pengobatan pasca bedah dan lain-lain mempunyai peranan penting, sehingga pemberian kaca mata afakia sebaiknya ditinjau kasus perkasus.
Selama ini di RS Cipto Mangunkusumo pemberian kaca mata afakia setelah 2 bulan pasca bedah di mana dianggap luka operasi sudah tenang dan hasil refraksi objektif dan subjektif sudah optimal.
Timbul masaalah pada penderita-penderita yang masih aktif bekerja agar dapat menjalankan fungsinya sedini mungkin sehingga mereka sangat mengharapkan kaca mata afakia secepatnya.
Kapan sebaiknya kaca mata afakia dapat diberikan merupakan hal yang perlu dikemukakan mengingat faktor-faktor tersebut diatas. Dalam hal ini penulis ingin mencoba untuk menentukan suatu kriteria, kapan sebaiknya diberikan kaca mata afakia pada penderita pasca bedah katarak yang tentu saja disesuaikan dengan kondisi dan situasi yang tersedia.
Pada penelitian ini penulis membatasi diri dengan hanya melakukan penelitian pada penderita yang dilakukan operasi katarak intrakapsuler dengan tehnik operasi yang sesuai protokol yang telah dianjurkan pada resider tingkat terakhir di Bagian Ilmu Penyakit mata RSCM.
"
1985
T-Pdf
UI - Tesis Membership  Universitas Indonesia Library
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Novita Christine
"Tujuan: Membandingkan rerata dan proporsi ≤ 1 D dari prediktabilitas refraksi biometri imersi terhadap biometri optikal pasca fakoemulsifikasi pada pasien katarak dengan miopia tinggi ( Spherical equivalent [SE] lebih besar atau sama dengan -6 atau AXl ≥ 25 mm) tanpa stafiloma posterior di RSCM Kirana.
Desain: Uji eksperimental tidak tersamar dua kelompok tidak berpasangan yang mendapat perlakuan biometri imersi dan optikal.
Metode: 21 mata dari 15 subyek yang dilakukan pemeriksaan biometri imersi dan optikal pada mata yang sama sebelum dilakukan operasi fakoemulsifikasi dengan implantasi lensa intraokular (LIO) posterior chamber. Target refraksi yang ditentukan adalah -0,5 D, dan power LIO yang diimplantasikan berasal dari pengukuran biometri imersi. Formula yang digunakan adalah SRK/T. Prediktabilitas refraksi dihitung berdasarkan selisih antara SE pasca operasi dengan target refraksi dalam nilai absolut pada minggu ke-3 pasca operasi.
Hasil: Tidak terdapat perbedaan yang bermakna pada rerata prediktabilitas refraksi (0,375 D ; 0,440 D, p=0,942), proporsi ≤ 1 D (80,95% ; 80,95%, p=1,000), dan pada semua variabel biometri.
Kesimpulan: Dengan formula SRK/T, biometri imersi dan optikal menghasilkan keakuratan prediktabilitas refraksi yang setara pada pasien katarak dengan miopia tinggi tanpa stafiloma posterior.

Objectives: To compare the mean and proportion ≤ 1 D of refractive predictability of immersion and optical biometry post phacoemulsification in cataract with highly myopic eyes (spherical equivalent [SE] of -6 D or higher, or axial length ≥ 25 mm) without posterior staphyloma.
Methods: This was an experimental non blinding study of the two unpaired groups. 21 eyes from 15 subjects had a measurements of immersion and optical biometry on the same eye. The intended refraction target was -0,5 D and based on immersion biometry. SRK/T formula was used in all groups. Refractive predictability was defined as a difference between post operative SE and the intended refraction target in an absolute value in 3 weeks post operatively.
Results: There were no statistically significant difference in the mean of refractive predictability (0,375 D ; 0,440 D, p=0,942) and proportion in a range of ≤ 1 D (80,95% ; 80,95%, p=1,000) nor in all biometry variable between the study groups.
Conclusion: Immersion and optical biometry with SRK/T formula produce a similar accuracy of refractive predictability in cataract with highly myopic eyes without posterior staphyloma.
"
Jakarta: Fakultas Kedokteran Universitas Indonesia, 2014
SP-PDF
UI - Tugas Akhir  Universitas Indonesia Library
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Suci Istiqa Mustafa
"Penelitian ini merupakan uji eksperimental dengan tiga populasi berbeda dengan proses intervensi yang sama yaitu penetesan tropikamid 1% yang bertujuan untuk menilai fungsi dan struktur jaringan mata setelah penetesan tropikamid 1%. Sebanyak 90 subjek dibagi menjadi tiga kelompok berdasarkan usia dan diabetes melitus tipe 2. Dilakukan pemeriksaan diameter pupil, tajam penglihatan jauh dan dekat, tekanan intraokular, dan kedalaman bilik mata depan yang diukur pada menit ke-30, 60, dan 120 setelah penetesan. Hasil penelitian ini mendapatkan bahwa kelompok usia 20-40 tahun dan usia ≥ 60 tahun dengan DM kurang responsif terhadap tropikamid 1% dibanding usia ≥ 60 tahun non-DM.

This is a clinical experimental study in three different groups with one intervention. This study aimed to assess ocular functions and structures in normal and diabetic subjects. A total of 90 subjects were divided into three groups based on the description of age and present of type 2 diabetes mellitus. The evaluation of pupil diameter, visual acuity, intraocular pressure, and anterior chamber depth were assessed in 30, 60, and 120 minutes after 1% tropicamide instillation. The result is that in the 20-40 years old non-DM group and ≥ 60 years old with DM group are less responsive to 1% tropicamide than ≥ 60 years old non-DM group."
Depok: Universitas Indonesia, 2014
SP-Pdf
UI - Tugas Akhir  Universitas Indonesia Library
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Tri Rejeki Herdiana
"Tujuan tesis ini adalah untuk mengetahui proporsi, karakteristik, dan faktor risiko retinopati diabetik pada responden diabetes melitus di puskesmas Jakarta Timur dan Jakarta Selatan. Desain penelitian berbasis populasi, studi deskriptif-analitik dengan metode potong lintang. Kriteria inklusi adalah pasien diabetes melitus berusia > 18 tahun yang dilakukan pemeriksaan foto fundus di puskesmas kecamatan Jakarta Timur dan Jakarta Selatan. Dilakukan cluster random sampling dan didapatkan 17 kecamatan intervensi yang dilakukan pemeriksaan foto fundus. Dilakukan consecutive sampling dengan pemberitahuan secara aktif kepada responden. Responden diperiksa foto fundus tanpa dilatasi dan retinopati digrading dengan menggunakan klasifikasi NSC (National Screening Committee). Responden diperiksa tajam penglihatan, tekanan darah, lingkar pinggang, lingkar panggul, pemeriksaan laboratorium, dan dilakukan wawancara terpimpin untuk evaluasi faktor risiko. Jumlah total sampel dari penelitian ini adalah 419 responden dengan proporsi retinopati diabetik adalah 49 responden (11.7%). Pada analisis multivariat, faktor risiko independen untuk DR adalah usia ≥ 60 saat datang (OR 0.46; 95% CI, 0.24-0.89), durasi DM ≥ 5 tahun (OR 1.43; 95% CI, 0.79-2.59), keturunan DM (+) (OR 1.89; 95% CI, 0.98-3.63), GDP ≥ 126mg/dl (OR 2.06; 95% CI, 0.95-4.44), penyakit komplikasi (+) (OR 1.41; 95% CI, 0.78-2.57), gangguan penglihatan ringan (OR 1.81; 95% CI, 0.84-3.88), lingkar pinggang berlebih (OR 0.39; 95% CI, 0.20-0.73). Responden dengan retinopati diabetik cenderung memiliki indeks massa tubuh normal, tanpa obesitas sentral, dengan lingkar pinggang normal. Berdasarkan data yang didapatkan, satu dari 10 responden diabetes melitus di puskesmas Jakarta Timur dan Jakarta Selatan memiliki retinopati diabetik. Faktor risiko independen yang berkaitan dengan retinopati diabetik adalah usia ≥ 60 tahun dan lingkar pinggang berlebih.

The purpose of this study was to describe the proportion, characteristics, and risk factors of diabetic retinopathy in diabetic population at primary health care (PHC) in East Jakarta and South Jakarta. Population-based cross sectional study, analytic ? descriptive. Method: Diabetic individuals > 18 years were screened for diabetic retinopathy with single field nonmydriatil 45o retinal photograph at PHC in East Jakarta and South Jakarta and retinopathy was graded in NSC (National Screening Committee) system. We had cluster random sampling for 34 PHC and 17 were selected and performed retinal photography for DR screening. Consecutive sampling was performed with active announcement for diabetic patients in PHC within the scope of the study. All participants underwent guided interview and examination including uncorrected visual acuity, blood pressure, waist-hip circumference, body mass index, and collection of blood samples. Results : We had 419 diabetic person who participated in this study. The overall proportion of DR was 49 (11.7%). In logistic regression analysis, independent risk factors for DR were age ≥ 60 years (OR 0.46; 95% CI, 0.24-0.89), diabetic duration ≥ 5 years (OR 1.43; 95% CI, 0.792.59), related to diabetes mellitus (OR 1.89; 95% CI, 0.98-3.63), fasting blood glucose ≥ 126mg/dl (OR 2.06; 95% CI, 0.95-4.44), complications of diabetes (OR 1.41; 95% CI, 0.78-2.57), mild visual acuity disturbance (OR 1.81; 95% CI, 0.84-3.88), excessive waist circumference (OR 0.39; 95% CI, 0.20-0.73). Person with DR tend to have normal body mass index, without central obesity, with a normal waist circumference. Conclusion : One in 10 adults with diabetes at PHC in East Jakarta and South Jakarta has diabetic retinopathy. The independent association of DR with established risk factors were age more than or equal to 60 years old and excessive waist circumference."
Depok: Universitas Indonesia, 2015
SP-Pdf
UI - Tugas Akhir  Universitas Indonesia Library
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Faresa Hilda
"ABSTRAK
Tujuan tesis ini adalah mengetahui pengaruh laser fotokoagulasi panretinal 532 nm durasi 20 ms dosis tunggal, 100 ms dosis tunggal dan 100 ms-3 sesi terhadap ketebalan makula sentral (KMS). Desain penelitian adalah uji klinis acak terkontrol tersamar ganda. Tiga puluh tiga mata yang memenuhi kriteria inklusi dirandomisasi untuk mendapatkan laser 20 ms dosis tunggal atau 100 ms dosis tunggal atau 100 ms-3 sesi. Keluaran primer adalah KMS yang diukur menggunakan time-domain Optical Coherence Tomography pada baseline, 4 minggu dan 8 minggu pasca laser. Analisis hasil didapatkan rerata ( + SE) KMS baseline kelompok 100 ms, 20 ms dan 100 ms-3 sesi berturut-turut adalah 212,18 + 12,18 µm; 199,18 + 12,18 µm; 215,36 + 12,18 µm. Empat minggu pasca laser, KMS berturut-turut meningkat menjadi 232,09 + 18,63 µm; 206,27 + 18,63 µm; 254,09 + 18,63 µm. Delapan minggu pasca laser, KMS meningkat pada kelompok 100 ms dan 20 ms (237,90 + 17,47 µm; 208,27 + 17,47 µm), namun menurun pada kelompok 100 ms-3sesi (252,36 + 17,47 µm).

ABSTRACT
The purpose of this study was to determine the effect of panretinal laser photocoagulation 532 nm of 20 ms duration single session (SS), 100 ms SS and 100 ms (3 session) toward central macular thickness (CMT). The study design was a double-blind, randomized controlled clinical trial. Thirty-three subjects who met inclusion criteria were randomized to receive 20 ms SS laser or 100 ms SS or 100 ms (3 session). Primary output was CMT, measured by time-domain Optical Coherence Tomography at baseline, 4 weeks and 8 weeks post-laser. Results showed mean ( + SE) CMT at baseline from 100 ms SS group, 20 ms SS and 100 ms-3 session were 212.18 + 12.18 μm; 199.18 + 12.18 μm; 215.36 + 12.18 μm respectively. Four weeks after laser, CMT was increased to 232.09 + 18.63 μm; 206.27 + 18.63 μm; 254.09 + 18.63 μm respectively. Eight weeks post laser, CMT was increased in 100 ms SS and 20 ms SS (237.90 + 17.47 μm; 208.27 + 17.47 μm), but decreased 100 ms-3session group (252.36 + 17.47 μm).
"
Jakarta: Fakultas Kedokteran Universitas Indonesia, 2015
SP-PDF
UI - Tugas Akhir  Universitas Indonesia Library
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Alia Arianti
"ABSTRAK
Tesis ini bertujuan menilai perbandingan efektivitas injeksi intravitreal
vorikonazol 100 µg/0.1 mL dengan amfoterisin B 5 µg/0.1 mL pada endoftalmitis
akibat Aspergillus flavus di hewan coba kelinci. Uji eksperimental tersamar acak
dilakukan pada 15 kelinci albino New Zealand white yang terbagi menjadi tiga
kelompok, yaitu kelompok vorikonazol, amfoterisin B, dan kontrol. Parameter
yang dinilai adalah perubahan klinis, pemeriksaan mikologi, dan perubahan
histopatologi jaringan. Perubahan skor klinis di akhir evaluasi tidak berbeda
bermakna antara kelompok vorikonazol dengan amfoterisin B, namun respons
klinis cenderung lebih baik pada kelompok vorikonazol. Jumlah koloni jamur
terkecil dan berbeda bermakna didapatkan pada kelompok amfoterisin B. Tidak
didapatkan perbedaan bermakna pada rerata nilai histopatologi jaringan kedua
kelompok, namun derajat inflamasi cenderung lebih ringan pada kelompok vorikonazol.ABSTRACT
The purpose of this study was to compare the efficacies of intravitreal 100 µg voriconazole and 5 µg amphotericin B treatment against Aspergillus flavus in an
exogenous endophthalmitis model in rabbit eyes. A randomized, controlledexperimental
study was conducted on 15 albino New Zealand white rabbits, which latter allocated into three different
treatment group of voriconazole, amphotericin B, and control. Clinical grading were performed at multiple times, while mycology analysis and histopathological examination were performed at 10 days
after treatment. No significant change in clinical grading was found between the
treatment group, but voriconazole group showed better response tendency. The smallest number of fungal colony forming unit was found significantly in the
amphotericin B group. No significant difference was found, however, between the mean histopathological score of the two treatment groups, but the tendency of a lower inflammation score was shown in voriconazole group. ;The purpose of this study was to compare the efficacies of intravitreal 100 µg
voriconazole and 5 µg amphotericin B treatment against Aspergillus flavus in an
exogenous endophthalmitis model in rabbit eyes. A randomized, controlledexperimental
study
was
conducted
on
15
albino
New
Zealand
white
rabbits,
which
latter
allocated
into
three
different
treatment
group
of
voriconazole,
amphotericin
B,
and control. Clinical grading were performed at multiple times, while
mycology analysis and histopathological examination were performed at 10 days
after treatment. No significant change in clinical grading was found between the
treatment group, but voriconazole group showed better response tendency. The
smallest number of fungal colony forming unit was found significantly in the
amphotericin B group. No significant difference was found, however, between the
mean histopathological score of the two treatment groups, but the tendency of a lower inflammation score was shown in voriconazole group. ;The purpose of this study was to compare the efficacies of intravitreal 100 µg
voriconazole and 5 µg amphotericin B treatment against Aspergillus flavus in an
exogenous endophthalmitis model in rabbit eyes. A randomized, controlledexperimental
study
was
conducted
on
15
albino
New
Zealand
white
rabbits,
which
latter
allocated
into
three
different
treatment
group
of
voriconazole,
amphotericin
B,
and control. Clinical grading were performed at multiple times, while
mycology analysis and histopathological examination were performed at 10 days
after treatment. No significant change in clinical grading was found between the
treatment group, but voriconazole group showed better response tendency. The
smallest number of fungal colony forming unit was found significantly in the
amphotericin B group. No significant difference was found, however, between the
mean histopathological score of the two treatment groups, but the tendency of a lower inflammation score was shown in voriconazole group. ;The purpose of this study was to compare the efficacies of intravitreal 100 µg
voriconazole and 5 µg amphotericin B treatment against Aspergillus flavus in an
exogenous endophthalmitis model in rabbit eyes. A randomized, controlledexperimental
study
was
conducted
on
15
albino
New
Zealand
white
rabbits,
which
latter
allocated
into
three
different
treatment
group
of
voriconazole,
amphotericin
B,
and control. Clinical grading were performed at multiple times, while
mycology analysis and histopathological examination were performed at 10 days
after treatment. No significant change in clinical grading was found between the
treatment group, but voriconazole group showed better response tendency. The
smallest number of fungal colony forming unit was found significantly in the
amphotericin B group. No significant difference was found, however, between the
mean histopathological score of the two treatment groups, but the tendency of a lower inflammation score was shown in voriconazole group. "
Fakultas Kedokteran Universitas Indonesia, 2015
SP-PDF
UI - Tugas Akhir  Universitas Indonesia Library
cover
Seruni Era Lestari
"ABSTRAK
Penelitian ini bertujuan untuk menilai akurasi skrining ROP bayi prematur dengan
menggunakan wide field retinal imaging system (RetCam
vi
®
) yang dilakukan oleh
dokter umum terlatih dibandingkan dengan menggunakan oftalmoskopi indirek
binokuler (BIO). Penelitian ini merupakan penelitian potong lintang dan bersifat uji
diagnostik. Semua bayi prematur yang memenuhi kriteria skrining menurut workshop
ROP dan bayi prematur di Indonesia diikutsertakan pada penelitian ini. Pada
penelitian ini didapatkan hasil bahwa WFDRI (RetCam
®
) yang dilakukan oleh dokter
umum yang terlatih secara baku sama akuratnya dengan oftalmoskopi indirek
binokuler (BIO) dalam skrining ROP pada bayi lahir prematur.ABSTRACT
The aim of this study was to evaluate the accuracy of wide field digital retinal
imaging (RetCam
®) conducted by trained general practitioner in comparison with
binocular indirect ophthalmoscopy (BIO). The design of this study was a cross
sectional, diagnostic trial study. Preterm infants that met the inclusion criteria
according to Indonesia retinopathy of prematurity workshop were included in the
study. The result of this study revealed that the accuracy of WFDRI (RetCam
)
performed by trained general practitioner were similar to those performed using BIO
in ROP screening.;The aim of this study was to evaluate the accuracy of wide field digital retinal
imaging (RetCam
®
) conducted by trained general practitioner in comparison with
binocular indirect ophthalmoscopy (BIO). The design of this study was a cross
sectional, diagnostic trial study. Preterm infants that met the inclusion criteria
according to Indonesia retinopathy of prematurity workshop were included in the
study. The result of this study revealed that the accuracy of WFDRI (RetCam
)
performed by trained general practitioner were similar to those performed using BIO
in ROP screening.;The aim of this study was to evaluate the accuracy of wide field digital retinal
imaging (RetCam
®
) conducted by trained general practitioner in comparison with
binocular indirect ophthalmoscopy (BIO). The design of this study was a cross
sectional, diagnostic trial study. Preterm infants that met the inclusion criteria
according to Indonesia retinopathy of prematurity workshop were included in the
study. The result of this study revealed that the accuracy of WFDRI (RetCam
)
performed by trained general practitioner were similar to those performed using BIO
in ROP screening.;The aim of this study was to evaluate the accuracy of wide field digital retinal
imaging (RetCam
®
) conducted by trained general practitioner in comparison with
binocular indirect ophthalmoscopy (BIO). The design of this study was a cross
sectional, diagnostic trial study. Preterm infants that met the inclusion criteria
according to Indonesia retinopathy of prematurity workshop were included in the
study. The result of this study revealed that the accuracy of WFDRI (RetCam
)
performed by trained general practitioner were similar to those performed using BIO
in ROP screening."
Fakultas Kedokteran Universitas Indonesia, 2015
SP-PDF
UI - Tugas Akhir  Universitas Indonesia Library
cover
Asri Setiawati
"ABSTRAK
Latar Belakang: Banyaknya jumlah kasus ROP yang terlambat dirujuk ke RSCM-Kirana menunjukkan bahwa penanganan ROP di Indonesia masih
merupakan tantangan. Keterlambatan diagnosis ROP yang ditemukan di RSCM tersebut dapat disebabkan oleh terbatasnya dokter mata ahli retina dan pediatric ophthalmologist (PO) dan kurangnya pengetahuan dokter mata umum dalam
mendiagnosis ROP. Pengetahuan dan keterampilan mendiagnosis ROP
merupakan salah satu mata ajar dalam program pendidikan dokter spesialis mata
di FKUI. Data mengenai seberapa baik pengetahuan PPDS tersebut dalam
mendiagnosis ROP belum tersedia.
Tujuan: Mengevaluasi kemampuan PPDS mata dalam mendiagnosis ROP
berdasarkan pembacaan hasil foto wide field digital retinal imaging (WFDRI)
bayi prematur.
Metode: Sebanyak 25 set foto WFDRI dibaca dan diinterpretasi oleh 15 subjek
PPDS mata, dan digolongkan ke dalam 4 klasifikasi: tidak ada ROP, ROP ringan,
ROP tipe 2, dan ROP yang memerlukan terapi. Pembacaan oleh subjek tersebut
dihitung nilai kesesuaiannya (Kappa) terhadap pembacaan oleh 3 konsultan PO
sebagai referensi, kemudian ditentukan tingkat kesesuaian berdasarkan
penggolongan nilai Kappa. Tingkat kesesuaian yang diharapkan adalah ?sangat
baik?, khusus untuk penentuan ROP perlu terapi, nilai Kappa yang diharapkan
adalah 1,00.
Hasil: Dalam penentuan adanya ROP, seluruh subjek memiliki tingkat kesesuaian
?sangat baik? (Kappa 1,00); dalam penentuan ROP ringan atau lebih berat, hanya
1 dari 15 subjek memiliki tingkat kesesuaian ?sangat baik?, 9 subjek memiliki
kesesuaian ?baik?, dan 5 subjek memiliki kesesuian ?sedang? (Kappa 0,65+0,15);
dalam penentuan ROP tipe 2 atau lebih berat, 10 dari 15 subjek memiliki tingkat
kesesuaian ?sangat baik?, 3 subjek memiliki kesesuaian ?baik?, dan 2 subjek
memiliki kesesuaian ?sedang? (Kappa 0,45-1,00); dalam penentuan ROP yang
memerlukan terapi, hanya 7 dari 15 subjek yang memiliki nilai Kappa 1,00,
namun 12 dari 15 subjek memiliki tingkat kesesuaian ?sangat baik?, dan 3 subjek
memiliki kesesuaian ?baik? (Kappa 0,75-1,00). Dalam penentuan zona dan
stadium, hanya sebagian kecil subjek yang memiliki tingkat kesesuaian ?sangat
baik? (Kappa 0,35-0,81 dan 0,32-0,91); sedangkan dalam penentuan plus disease,
hanya 6 dari 15 subjek yang memiliki nilai Kappa 1,00.
Kesimpulan: Kemampuan PPDS mata dalam mendiagosis ROP belum
seluruhnya mencapai target yang diharapkan. ABSTRACT
Background: Numerous late-stage ROP cases that referred to Cipto
Mangunkusumo Hospital (Kirana) showed us that ROP management in Indonesia
is still a challenge. The delayed management might be caused by limited number
of vitreoretinal specialist or pediatric ophthalmologist, and inadequate diagnostic
knowledge of ROP of the general ophthalmologists. In condition of limited
number of vitreoretinal and pediatric ophthalmologists, the general
ophthalmologists are suggested to be taking part in ROP screening program. In
FKUI, ROP screening has been a part of residency training program, however,
there was no available data of ROP diagnostic knowledge of the residents.
Purpose: To measure agreement of image-based ROP diagnosis between
ophthalmology residents and pediatric ophthalmologist.
Methods: Twenty-five sets of retinal photographs of premature infants were
interpreted by 15 ophthalmology residents and pediatric ophthalmologists, and
classified into 4 categories: no ROP, mild ROP, type 2 ROP, and treatmentrequiring
ROP.
Agreements
are
measured
for
diagnosis
classification,
stage,
zone,
and
plus disease detection. Level of agreement was measured based on Kappa
value of each subjects. The expected level of agreement for each category was
?very good agreement?. For treatment-requiring ROP and plus disease, the
expected Kappa value was 1.00.
Results: For detection of no ROP, agreement of all subjects was ?very good?
(Kappa 1,00); for detection of mild or worse ROP, only 1 of 15 subjects has ?very
good agreement?, 9 of 15 subjects have ?good agreement?, and 5 subjects have
?moderate agreement? (Kappa 0,65+0,15); for detection of type 2 or worse ROP,
10 of 15 subjects have ?very good agreement?, 3 subjects have ?good agreement?,
and 2 subjects have ?moderate agreement? (Kappa 0,45-1,00); for detection of
requiring-therapy ROP, only 7 of 15 subjects that have Kappa value of 1.00,
however, 12 of 15 subjects have ?very good agreement?, and only 3 subjects have
?good agreement? (Kappa 0,75-1,00). For detection of stage and zone of ROP,
only a little number of subjects have ?very good agreement? (Kappa 0.35-0.81,
and 0.32-0.91, respectively); and for plus disease detection, only 6 of 15 subjects
have Kappa value of 1.00.
Conclusion: Agreement of image-based ROP diagnosis between ophthalmology
residents and pediatric ophthalmologist has not achieved the expected target yet. ;Background: Numerous late-stage ROP cases that referred to Cipto
Mangunkusumo Hospital (Kirana) showed us that ROP management in Indonesia
is still a challenge. The delayed management might be caused by limited number
of vitreoretinal specialist or pediatric ophthalmologist, and inadequate diagnostic
knowledge of ROP of the general ophthalmologists. In condition of limited
number of vitreoretinal and pediatric ophthalmologists, the general
ophthalmologists are suggested to be taking part in ROP screening program. In
FKUI, ROP screening has been a part of residency training program, however,
there was no available data of ROP diagnostic knowledge of the residents.
Purpose: To measure agreement of image-based ROP diagnosis between
ophthalmology residents and pediatric ophthalmologist.
Methods: Twenty-five sets of retinal photographs of premature infants were
interpreted by 15 ophthalmology residents and pediatric ophthalmologists, and
classified into 4 categories: no ROP, mild ROP, type 2 ROP, and treatmentrequiring
ROP.
Agreements
are
measured
for
diagnosis
classification,
stage,
zone,
and
plus disease detection. Level of agreement was measured based on Kappa
value of each subjects. The expected level of agreement for each category was
?very good agreement?. For treatment-requiring ROP and plus disease, the
expected Kappa value was 1.00.
Results: For detection of no ROP, agreement of all subjects was ?very good?
(Kappa 1,00); for detection of mild or worse ROP, only 1 of 15 subjects has ?very
good agreement?, 9 of 15 subjects have ?good agreement?, and 5 subjects have
?moderate agreement? (Kappa 0,65+0,15); for detection of type 2 or worse ROP,
10 of 15 subjects have ?very good agreement?, 3 subjects have ?good agreement?,
and 2 subjects have ?moderate agreement? (Kappa 0,45-1,00); for detection of
requiring-therapy ROP, only 7 of 15 subjects that have Kappa value of 1.00,
however, 12 of 15 subjects have ?very good agreement?, and only 3 subjects have
?good agreement? (Kappa 0,75-1,00). For detection of stage and zone of ROP,
only a little number of subjects have ?very good agreement? (Kappa 0.35-0.81,
and 0.32-0.91, respectively); and for plus disease detection, only 6 of 15 subjects
have Kappa value of 1.00.
Conclusion: Agreement of image-based ROP diagnosis between ophthalmology
residents and pediatric ophthalmologist has not achieved the expected target yet. ;Background: Numerous late-stage ROP cases that referred to Cipto
Mangunkusumo Hospital (Kirana) showed us that ROP management in Indonesia
is still a challenge. The delayed management might be caused by limited number
of vitreoretinal specialist or pediatric ophthalmologist, and inadequate diagnostic
knowledge of ROP of the general ophthalmologists. In condition of limited
number of vitreoretinal and pediatric ophthalmologists, the general
ophthalmologists are suggested to be taking part in ROP screening program. In
FKUI, ROP screening has been a part of residency training program, however,
there was no available data of ROP diagnostic knowledge of the residents.
Purpose: To measure agreement of image-based ROP diagnosis between
ophthalmology residents and pediatric ophthalmologist.
Methods: Twenty-five sets of retinal photographs of premature infants were
interpreted by 15 ophthalmology residents and pediatric ophthalmologists, and
classified into 4 categories: no ROP, mild ROP, type 2 ROP, and treatmentrequiring
ROP.
Agreements
are
measured
for
diagnosis
classification,
stage,
zone,
and
plus disease detection. Level of agreement was measured based on Kappa
value of each subjects. The expected level of agreement for each category was
?very good agreement?. For treatment-requiring ROP and plus disease, the
expected Kappa value was 1.00.
Results: For detection of no ROP, agreement of all subjects was ?very good?
(Kappa 1,00); for detection of mild or worse ROP, only 1 of 15 subjects has ?very
good agreement?, 9 of 15 subjects have ?good agreement?, and 5 subjects have
?moderate agreement? (Kappa 0,65+0,15); for detection of type 2 or worse ROP,
10 of 15 subjects have ?very good agreement?, 3 subjects have ?good agreement?,
and 2 subjects have ?moderate agreement? (Kappa 0,45-1,00); for detection of
requiring-therapy ROP, only 7 of 15 subjects that have Kappa value of 1.00,
however, 12 of 15 subjects have ?very good agreement?, and only 3 subjects have
?good agreement? (Kappa 0,75-1,00). For detection of stage and zone of ROP,
only a little number of subjects have ?very good agreement? (Kappa 0.35-0.81,
and 0.32-0.91, respectively); and for plus disease detection, only 6 of 15 subjects
have Kappa value of 1.00.
Conclusion: Agreement of image-based ROP diagnosis between ophthalmology
residents and pediatric ophthalmologist has not achieved the expected target yet. "
Fakultas Kedokteran Universitas Indonesia, 2016
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UI - Tugas Akhir  Universitas Indonesia Library
cover
Damara Andalia
"ABSTRAK
Latar belakang Glaukoma masih merupakan salah satu penyebab kebutaan
terbesar di dunia. Belakangan ini, ketebalan RFNL dan GCIPL diketahui memiliki
hubungan terhadap perubahan struktural yang disebabkan oleh glaukoma.
Tujuan untuk mengkaji kemampuan diagnostik dari pengukuran ketebalan RFNL
dan GCIPL dalam mendeteksi glaukoma pada tahap awal.
Metode Enam puluh empat mata dengan sudut bilik mata sempit (32 glaukoma,
32 non-glaukoma) dari 48 pasien menjalani pengukuran menggunakan Cirrus
OCT dengan protokol 3,4 mm pemindaian cepat RFNL peripapilar. Pengukuran
dilakukan pada sisi superior, inferior, nasal, temporal dari GCIPL dan RFNL,
begitu juga dengan GCIPL superotemporal, superonasal, inferotemporal,
inferonasal, dan minimal.
Hasil Semua parameter yang diuji pada studi ini menunjukkan angka yang lebih
rendah pada kelompok PACG dibandingkan kelompok PAC. Rerata ketebalan
RFNL dan ketebalan GCIPL inferotemporal masing-masing memiliki nilai
spesifitias dan sensitifitas yang paling baik. Parameter dengan determinan terbaik
adalah ketebalan GCIPL inferotemporal dengan sensitifitas dan spesifitas masingmasing
75%
dan
75%.
Kesimpulan
Ketebalan GCIPL dan RFNL peripapil memiliki potensi besar
sebagai parameter diagnostik seperti skrining dan evaluasi respon terapi.
ABSTRACT
Background Glaucoma remains one of the biggest causes of blindness
worldwide. Recently, RFNL and GCIPL thickness were shown to be correlated
with early structural changes caused by glaucoma.
Objective to evaluate the diagnostic performance of RFNL and GCIPL thickness
measurement in detecting early glaucoma
Method Sixty-four eyes with primary angle closure (32 glaucomatous, 32 nonglaucomatous)
of
48
patients underwent peripapillar scanning using Cirrus OCT
using 3,4 mm protocol fast RNFL peripapillary thickness scan. The measurement
includes superior, inferior, nasal, temporal, mean GCIPL and RFNL, as well as
superotemporal, superonasal, inferotemporal, inferonasal, minimal GCIPL.
Result All parameters studied were significantly thinner in PACG group
compared to PAC group. Mean RFNL thickness and inferotemporal GCIPL has
the highest specificity and sensitivity, respectively, in detecting glaucoma.
Parameter with the best determinant is inferotemporal GCIPL thickness with
sensitivity and specificity, 75% and 71.9%, respectively.
Conclusion Peripapillary RFNL and GCIPL could be a potential diagnostic
parameter in detecting early glaucoma and monitoring therapy response in
glaucoma patients. ;Background Glaucoma remains one of the biggest causes of blindness
worldwide. Recently, RFNL and GCIPL thickness were shown to be correlated
with early structural changes caused by glaucoma.
Objective to evaluate the diagnostic performance of RFNL and GCIPL thickness
measurement in detecting early glaucoma
Method Sixty-four eyes with primary angle closure (32 glaucomatous, 32 nonglaucomatous)
of
48
patients underwent peripapillar scanning using Cirrus OCT
using 3,4 mm protocol fast RNFL peripapillary thickness scan. The measurement
includes superior, inferior, nasal, temporal, mean GCIPL and RFNL, as well as
superotemporal, superonasal, inferotemporal, inferonasal, minimal GCIPL.
Result All parameters studied were significantly thinner in PACG group
compared to PAC group. Mean RFNL thickness and inferotemporal GCIPL has
the highest specificity and sensitivity, respectively, in detecting glaucoma.
Parameter with the best determinant is inferotemporal GCIPL thickness with
sensitivity and specificity, 75% and 71.9%, respectively.
Conclusion Peripapillary RFNL and GCIPL could be a potential diagnostic
parameter in detecting early glaucoma and monitoring therapy response in
glaucoma patients. ;Background Glaucoma remains one of the biggest causes of blindness
worldwide. Recently, RFNL and GCIPL thickness were shown to be correlated
with early structural changes caused by glaucoma.
Objective to evaluate the diagnostic performance of RFNL and GCIPL thickness
measurement in detecting early glaucoma
Method Sixty-four eyes with primary angle closure (32 glaucomatous, 32 nonglaucomatous)
of
48
patients underwent peripapillar scanning using Cirrus OCT
using 3,4 mm protocol fast RNFL peripapillary thickness scan. The measurement
includes superior, inferior, nasal, temporal, mean GCIPL and RFNL, as well as
superotemporal, superonasal, inferotemporal, inferonasal, minimal GCIPL.
Result All parameters studied were significantly thinner in PACG group
compared to PAC group. Mean RFNL thickness and inferotemporal GCIPL has
the highest specificity and sensitivity, respectively, in detecting glaucoma.
Parameter with the best determinant is inferotemporal GCIPL thickness with
sensitivity and specificity, 75% and 71.9%, respectively.
Conclusion Peripapillary RFNL and GCIPL could be a potential diagnostic
parameter in detecting early glaucoma and monitoring therapy response in
glaucoma patients. "
Fakultas Kedokteran Universitas Indonesia, 2015
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UI - Tugas Akhir  Universitas Indonesia Library
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