Implementasi Program Skrining Hipotiroid Kongenital (HKI) pada Bayi Baru Lahir di Kabupaten Jember

DOI: 10.29241/jmk.v11i1.2080

Author

Ana Silfia Margareta(1*)

(1) Universitas Jember, Jawa Timur, Indonesia
(1*) Corresponding Author

Full Text

Full Text: View / Download PDF

Article Metrics

Abstract View : 9 times; PDF Download : 5 times

Abstract

  1. Congenital hypothyroidism has a serious impact on cognitive and physical development if not detected and treated promptly. Most cases are permanent and result in adverse effects. This study aims to determine the success of the implementation of Congenital Hypothyroidism (CHS) screening in Jember Regency. This type of research is qualitative with an in-depth interview design. The objects in this study were 13 informants and 1 triangulation informant. This research was conducted in Jember Regency in August 2024. The instrument used was an in-depth interview guide. Data analysis used data reduction. The results of the study showed that the SHK program had been implemented in accordance with the policy, but the achievement of SHK implementation was still low. This is influenced by factors of human resources, funding sources, inadequate facilities and infrastructure. It is recommended that there is a need for integration of the implementation of other programs that can support the SHK program with the same goal, namely early detection of congenital hypothyroidism in newborns

Keywords

Newborns, Implementation, Congenital Hypothyroidism Screening

References

Alm, J., Larsson, & Zetterstrom, R. (1978). Hipotiroidisme kongenital di Swedia. Insiden dan usia saat diagnosis. Acta Paediatrica, 67(1), 1-3. https://doi.org/https://doi.org/10.1111/j.1651-2227.1978.tb16268.x
https://doi.org/10.1111/j.1651-2227.1978.tb16268.x Anggraini, A., Suryawati, C., & Fatmasari, E. Y. (2019). Evaluasi Pelaksanaan Program Skrining Hipotiroid Kongenital oleh Puskesmas Karangrejo Kota Metro, Lampung. Jurnal Kesehatan Masyarakat (e-journal), 7(1), 1-11. Anggraini, R., Patria, S. Y., & Julia, M. (2017). Ketepatan Waktu Pelayanan Skrining Hipotiroidism Kongenital di Yogyakarta. Sari Pediatr, 18(6), 436-442.
https://doi.org/10.14238/sp18.6.2017.436-42 Ariani, Y., Soeharso, P., & Sjarif, D. R. (2017). Genetics and genomic medicine in Indonesia. Mol. Genet. Genom. Med, 5(2), 103-109.
https://doi.org/10.1002/mgg3.284 Bradford, L. T., & Jrand-Carmencita, D. P. (2018). Newborn screening in The developing countries. Curr Opin Pediatr, 30(6).
https://doi.org/10.1097/MOP.0000000000000683 Dumilah, R., Yulifah, R., Mansur, H., Suprapti, S., & Darwanty, U. (2023). Implementasi Pelaksanaan Program Skrining Hipotiroid Kongenital (SHK): Literature Review. Jurnal Media Penelitian dan Pengambangan Kesehatan, 33(4), 168-178.
https://doi.org/10.34011/jmp2k.v33i4.1810 Gaudino, R., Garel, C., Czernichow, P., & Léger, J. (2005). Proportion of various types of thyroid disorders among newborns with congenital hypothyroidism and normally located gland: a regional cohort study. Clinical Endocrinology, 62(4), 444-448. https://doi.org/https://translate.google.com/website?sl=en&tl=id&hl=id&client=wa&u=https://doi.org/10.1111/j.1365-2265.2005.02239.x
https://doi.org/10.1111/j.1365-2265.2005.02239.x Harris, K. B., & Pass, K. A. (2007). Increase in congenital hypothyroidism in New York State and in the United States. Molecular Genetics and Metabolism, 91(3), 268-277. https://doi.org/https://translate.google.com/website?sl=en&tl=id&hl=id&client=wa&u=https://doi.org/10.1016/j.ymgme.2007.03.012
https://doi.org/10.1016/j.ymgme.2007.03.012 Hiola, F. A. A., Hilamuhu, F., & Katili, D. N. O. (2022). Faktor-Faktor yang Mempengaruhi Cakupan Pelaksanaan Skrining Hipotiroid Kongenital di RSUProf. Dr. H. Aloe Saboe Kota Gorontalo. Media Publikasi Promosi Kesehatan Indonesia, 5(4), 435-440.
https://doi.org/10.56338/mppki.v5i4.2218 Kemenkes RI. (2014). Permenkes No 78 Tahun 2014 Skrinning Hipotiroid Kongenital. Kementerian Kesehatan Republik Indonesia. Latifah, L., Asturiningtyas, I. P., Nurcahyani, Ashar, D. Y., Sukanda, H., & Broto, P. (2020). Potensi Integrasi Program Skrining Hipotiroid pada Neonatal di Daerah Replete Defisiensi Iodium. Media Gizi Mikro Indonesia, 11(2), 153-168.
https://doi.org/10.22435/mgmi.v11i2.2676 Mansoor, S. (2020). Trends of congenital hypothyroidismand inborn errors of metabolism in Pakistan. Orphanet J Rare Dis, 15(1).
https://doi.org/10.1186/s13023-020-01602-6 Octavius, G. G. S., Daleni, & Sagala, V. . (2023). An Insight into Indonesia's Challenges in Implementing Newborn Screening Programs and Their Future Implications. Children, 10(7).
https://doi.org/10.3390/children10071216 Panatariono, T. A., & Puspitasari, Y. (2022). Determinan Faktor Terjadinya Stunting Pada Balita Di Desa Kambingan Timur Dan Desa Talang Kecamatan Saronggi Kabupaten Sumenep. Pengembangan Ilmu Dan Praktik Kesehatan, 1(1). https://doi.org/Https://Doi.Org/10.56586/Pipk.V1i1.187
https://doi.org/10.56586/pipk.v1i1.187 Setyaningsih, W., & Wulandari, R. D. (2022). The Evaluation of Congenital Hypothyroidism Screening Program in Indonesia: A Literature Review. Jurnal Aisyah: Jurnal Ilmu Kesehatan, 7(2), 495-502.
https://doi.org/10.30604/jika.v7i2.1161 Skordis, N., Toumba, M., Savva, S. C., Erakleous, E., Topouzi, M., Vogazianos, M., & Argyriou, A. (2005). High Prevalence of Congenital Hypothyroidism in the Greek Cypriot Population: Results of the Neonatal Screening Program 1990- 2000. Journal of Pediatric Oncology NursingEndocrinology and Metabolism, May. https://doi.org/https://doi.org/10.1515/JPEM.2005.18.5.453
https://doi.org/10.1515/JPEM.2005.18.5.453 Vandevijvere, S., Coucke, W., Vanderpas, J., Trumpff, C., Fauvart, M., Schoos, R., & et al. (2012). Neonatal Thyroid-Stimulating Hormone Concentrations in Belgium : A Useful Indicator for Detecting Mild Iodine Deficiency? PLoS One, 7(10), 3-8.
https://doi.org/10.1371/journal.pone.0047770 Wassner, A. J. (2017). Pediatric hypothyroidism: diagnosis and treatment. Paediatr Drugs, 19(4).
https://doi.org/10.1007/s40272-017-0238-0 Widayati, Susyati, & Purwanti. (2006). Uji Saring Hipotiroid Kongenital Melalui Kadar Neonatal - TSH dengan Teknik IRMA. Prosiding Pertemuan Ilmiah Fungsional Teknis Non Peneliti, 165-72. Yati, N. P., Utari, A., & Tridjaja, B. (2017). Panduan Praktik Klinis: Diagnosis dan Tata Laksana Hipotiroid Kongenital. Ikatan Dokter Anak Indonesia. Zdraveska, N., Kocova, M., Nicholas, A. K., Anastasovska, V., & Schoenmakers, N. (2020). Genetics of Gland-in-situ or Hypoplastic Congenital Hypothyroidismin Macedonia. Front. Endocrinol, 11(413).
https://doi.org/10.3389/fendo.2020.00413 Alm, J., Larsson, & Zetterstrom, R. (1978). Hipotiroidisme kongenital di Swedia. Insiden dan usia saat diagnosis. Acta Paediatrica, 67(1), 1-3. https://doi.org/https://doi.org/10.1111/j.1651-2227.1978.tb16268.x
https://doi.org/10.1111/j.1651-2227.1978.tb16268.x Anggraini, A., Suryawati, C., & Fatmasari, E. Y. (2019). Evaluasi Pelaksanaan Program Skrining Hipotiroid Kongenital oleh Puskesmas Karangrejo Kota Metro, Lampung. Jurnal Kesehatan Masyarakat (e-journal), 7(1), 1-11. Anggraini, R., Patria, S. Y., & Julia, M. (2017). Ketepatan Waktu Pelayanan Skrining Hipotiroidism Kongenital di Yogyakarta. Sari Pediatr, 18(6), 436-442.
https://doi.org/10.14238/sp18.6.2017.436-42 Ariani, Y., Soeharso, P., & Sjarif, D. R. (2017). Genetics and genomic medicine in Indonesia. Mol. Genet. Genom. Med, 5(2), 103-109.
https://doi.org/10.1002/mgg3.284 Bradford, L. T., & Jrand-Carmencita, D. P. (2018). Newborn screening in The developing countries. Curr Opin Pediatr, 30(6).
https://doi.org/10.1097/MOP.0000000000000683 Dumilah, R., Yulifah, R., Mansur, H., Suprapti, S., & Darwanty, U. (2023). Implementasi Pelaksanaan Program Skrining Hipotiroid Kongenital (SHK): Literature Review. Jurnal Media Penelitian dan Pengambangan Kesehatan, 33(4), 168-178.
https://doi.org/10.34011/jmp2k.v33i4.1810 Gaudino, R., Garel, C., Czernichow, P., & Léger, J. (2005). Proportion of various types of thyroid disorders among newborns with congenital hypothyroidism and normally located gland: a regional cohort study. Clinical Endocrinology, 62(4), 444-448. https://doi.org/https://translate.google.com/website?sl=en&tl=id&hl=id&client=wa&u=https://doi.org/10.1111/j.1365-2265.2005.02239.x
https://doi.org/10.1111/j.1365-2265.2005.02239.x Harris, K. B., & Pass, K. A. (2007). Increase in congenital hypothyroidism in New York State and in the United States. Molecular Genetics and Metabolism, 91(3), 268-277. https://doi.org/https://translate.google.com/website?sl=en&tl=id&hl=id&client=wa&u=https://doi.org/10.1016/j.ymgme.2007.03.012
https://doi.org/10.1016/j.ymgme.2007.03.012 Hiola, F. A. A., Hilamuhu, F., & Katili, D. N. O. (2022). Faktor-Faktor yang Mempengaruhi Cakupan Pelaksanaan Skrining Hipotiroid Kongenital di RSUProf. Dr. H. Aloe Saboe Kota Gorontalo. Media Publikasi Promosi Kesehatan Indonesia, 5(4), 435-440.
https://doi.org/10.56338/mppki.v5i4.2218 Kemenkes RI. (2014). Permenkes No 78 Tahun 2014 Skrinning Hipotiroid Kongenital. Kementerian Kesehatan Republik Indonesia. Latifah, L., Asturiningtyas, I. P., Nurcahyani, Ashar, D. Y., Sukanda, H., & Broto, P. (2020). Potensi Integrasi Program Skrining Hipotiroid pada Neonatal di Daerah Replete Defisiensi Iodium. Media Gizi Mikro Indonesia, 11(2), 153-168.
https://doi.org/10.22435/mgmi.v11i2.2676 Mansoor, S. (2020). Trends of congenital hypothyroidismand inborn errors of metabolism in Pakistan. Orphanet J Rare Dis, 15(1).
https://doi.org/10.1186/s13023-020-01602-6 Octavius, G. G. S., Daleni, & Sagala, V. . (2023). An Insight into Indonesia's Challenges in Implementing Newborn Screening Programs and Their Future Implications. Children, 10(7).
https://doi.org/10.3390/children10071216 Panatariono, T. A., & Puspitasari, Y. (2022). Determinan Faktor Terjadinya Stunting Pada Balita Di Desa Kambingan Timur Dan Desa Talang Kecamatan Saronggi Kabupaten Sumenep. Pengembangan Ilmu Dan Praktik Kesehatan, 1(1). https://doi.org/Https://Doi.Org/10.56586/Pipk.V1i1.187
https://doi.org/10.56586/pipk.v1i1.187 Setyaningsih, W., & Wulandari, R. D. (2022). The Evaluation of Congenital Hypothyroidism Screening Program in Indonesia: A Literature Review. Jurnal Aisyah: Jurnal Ilmu Kesehatan, 7(2), 495-502.
https://doi.org/10.30604/jika.v7i2.1161 Skordis, N., Toumba, M., Savva, S. C., Erakleous, E., Topouzi, M., Vogazianos, M., & Argyriou, A. (2005). High Prevalence of Congenital Hypothyroidism in the Greek Cypriot Population: Results of the Neonatal Screening Program 1990- 2000. Journal of Pediatric Oncology NursingEndocrinology and Metabolism, May. https://doi.org/https://doi.org/10.1515/JPEM.2005.18.5.453
https://doi.org/10.1515/JPEM.2005.18.5.453 Vandevijvere, S., Coucke, W., Vanderpas, J., Trumpff, C., Fauvart, M., Schoos, R., & et al. (2012). Neonatal Thyroid-Stimulating Hormone Concentrations in Belgium : A Useful Indicator for Detecting Mild Iodine Deficiency? PLoS One, 7(10), 3-8.
https://doi.org/10.1371/journal.pone.0047770 Wassner, A. J. (2017). Pediatric hypothyroidism: diagnosis and treatment. Paediatr Drugs, 19(4).
https://doi.org/10.1007/s40272-017-0238-0 Widayati, Susyati, & Purwanti. (2006). Uji Saring Hipotiroid Kongenital Melalui Kadar Neonatal - TSH dengan Teknik IRMA. Prosiding Pertemuan Ilmiah Fungsional Teknis Non Peneliti, 165-72. Yati, N. P., Utari, A., & Tridjaja, B. (2017). Panduan Praktik Klinis: Diagnosis dan Tata Laksana Hipotiroid Kongenital. Ikatan Dokter Anak Indonesia. Zdraveska, N., Kocova, M., Nicholas, A. K., Anastasovska, V., & Schoenmakers, N. (2020). Genetics of Gland-in-situ or Hypoplastic Congenital Hypothyroidismin Macedonia. Front. Endocrinol, 11(413).
https://doi.org/10.3389/fendo.2020.00413

Refbacks

  • There are currently no refbacks.




Copyright (c) 2025 Ana Silfia Margareta

Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.