Cystic Fibrosis in Asia

Background: Cystic fibrosis (CF) is the most common inherited life-limiting illness in the Caucasian population. It is considered to be rare in Asia, but recent reports suggest that CF does occur in Asia. Methods: We carried out a questionnaire-based survey to determine the prevalence of CF across A...

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Main Authors: Shakil Ahmed, Gary Cheok, Anne EN Goh, Aye Han, SJ Hong, Wahyuni Indawati, ARM Lutful Kabir, S K Kabra, Harutai Kamalaporn, Hyung Young Kim, Shen Kunling, Sorasak Lochindarat, Mohammad Ashkan Moslehi, Anna Marie Nathan, Daniel Ng, Nguyen Ng The Phung, V Singh, Masato Takase, Rina Triasih, Zen-Kong Dai
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2020-01-01
Series:Pediatric Respirology and Critical Care Medicine
Subjects:
Online Access:https://journals.lww.com/10.4103/prcm.prcm_5_20
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author Shakil Ahmed
Gary Cheok
Anne EN Goh
Aye Han
SJ Hong
Wahyuni Indawati
ARM Lutful Kabir
S K Kabra
Harutai Kamalaporn
Hyung Young Kim
Shen Kunling
Sorasak Lochindarat
Mohammad Ashkan Moslehi
Anna Marie Nathan
Daniel Ng
Nguyen Ng The Phung
V Singh
Masato Takase
Rina Triasih
Zen-Kong Dai
author_facet Shakil Ahmed
Gary Cheok
Anne EN Goh
Aye Han
SJ Hong
Wahyuni Indawati
ARM Lutful Kabir
S K Kabra
Harutai Kamalaporn
Hyung Young Kim
Shen Kunling
Sorasak Lochindarat
Mohammad Ashkan Moslehi
Anna Marie Nathan
Daniel Ng
Nguyen Ng The Phung
V Singh
Masato Takase
Rina Triasih
Zen-Kong Dai
author_sort Shakil Ahmed
collection DOAJ
description Background: Cystic fibrosis (CF) is the most common inherited life-limiting illness in the Caucasian population. It is considered to be rare in Asia, but recent reports suggest that CF does occur in Asia. Methods: We carried out a questionnaire-based survey to determine the prevalence of CF across Asian countries and the diagnostic and therapeutic capabilities available in member countries. A questionnaire was sent to member countries of the Asian Pediatric Pulmonology Society. The questionnaire included the total number of children diagnosed with CF seen in the country and the available resources. available resources for diagnosis and management. Results: Fifteen countries responded to the questionnaire. Three countries/regions (Myanmar, Vietnam, and Macau) have not recorded any case of CF. The remaining 12 countries have recorded a variable number of cases which have also been reported in the literature. Sweat chloride testing facilities were available in all the countries except Taiwan that reported cases of CF. Some countries such as India and Bangladesh have developed their own indigenous method for sweat testing. Some countries have facilities for mutation testing. Basic medications such as pancreatic enzyme supplementation and antibiotics were available in all the countries where children with CF have been diagnosed. Inhaled antibiotics and dornase alfa were available only in a few countries. Some other countries reported using the injectable preparation of gentamicin and amikacin for inhalation therapy. Testing for genetic mutation wherever available showed a low frequency of the Delta F 508 mutation which is the most common mutation found in the Caucasian population. Only two countries (India and Japan) have formal CF associations for the affected community. Two countries Japan and China maintain a CF registry, whereas India already started the process of developing it. Conclusion: CF is increasingly being diagnosed over the past two decades in Asian countries. There is a need to create awareness among pediatricians and to develop regional or country-specific protocols and tools for the diagnosis and treatment of children with CF.
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spelling doaj-art-c7ffdb8f029b4c50ba75ced5d99c5d542025-08-20T02:18:57ZengWolters Kluwer Medknow PublicationsPediatric Respirology and Critical Care Medicine2543-03432543-03512020-01-014181210.4103/prcm.prcm_5_20Cystic Fibrosis in AsiaShakil AhmedGary CheokAnne EN GohAye HanSJ HongWahyuni IndawatiARM Lutful KabirS K KabraHarutai KamalapornHyung Young KimShen KunlingSorasak LochindaratMohammad Ashkan MoslehiAnna Marie NathanDaniel NgNguyen Ng The PhungV SinghMasato TakaseRina TriasihZen-Kong DaiBackground: Cystic fibrosis (CF) is the most common inherited life-limiting illness in the Caucasian population. It is considered to be rare in Asia, but recent reports suggest that CF does occur in Asia. Methods: We carried out a questionnaire-based survey to determine the prevalence of CF across Asian countries and the diagnostic and therapeutic capabilities available in member countries. A questionnaire was sent to member countries of the Asian Pediatric Pulmonology Society. The questionnaire included the total number of children diagnosed with CF seen in the country and the available resources. available resources for diagnosis and management. Results: Fifteen countries responded to the questionnaire. Three countries/regions (Myanmar, Vietnam, and Macau) have not recorded any case of CF. The remaining 12 countries have recorded a variable number of cases which have also been reported in the literature. Sweat chloride testing facilities were available in all the countries except Taiwan that reported cases of CF. Some countries such as India and Bangladesh have developed their own indigenous method for sweat testing. Some countries have facilities for mutation testing. Basic medications such as pancreatic enzyme supplementation and antibiotics were available in all the countries where children with CF have been diagnosed. Inhaled antibiotics and dornase alfa were available only in a few countries. Some other countries reported using the injectable preparation of gentamicin and amikacin for inhalation therapy. Testing for genetic mutation wherever available showed a low frequency of the Delta F 508 mutation which is the most common mutation found in the Caucasian population. Only two countries (India and Japan) have formal CF associations for the affected community. Two countries Japan and China maintain a CF registry, whereas India already started the process of developing it. Conclusion: CF is increasingly being diagnosed over the past two decades in Asian countries. There is a need to create awareness among pediatricians and to develop regional or country-specific protocols and tools for the diagnosis and treatment of children with CF.https://journals.lww.com/10.4103/prcm.prcm_5_20childcystic fibrosisdornase alfapancreatic enzymesweat testtobramycin
spellingShingle Shakil Ahmed
Gary Cheok
Anne EN Goh
Aye Han
SJ Hong
Wahyuni Indawati
ARM Lutful Kabir
S K Kabra
Harutai Kamalaporn
Hyung Young Kim
Shen Kunling
Sorasak Lochindarat
Mohammad Ashkan Moslehi
Anna Marie Nathan
Daniel Ng
Nguyen Ng The Phung
V Singh
Masato Takase
Rina Triasih
Zen-Kong Dai
Cystic Fibrosis in Asia
Pediatric Respirology and Critical Care Medicine
child
cystic fibrosis
dornase alfa
pancreatic enzyme
sweat test
tobramycin
title Cystic Fibrosis in Asia
title_full Cystic Fibrosis in Asia
title_fullStr Cystic Fibrosis in Asia
title_full_unstemmed Cystic Fibrosis in Asia
title_short Cystic Fibrosis in Asia
title_sort cystic fibrosis in asia
topic child
cystic fibrosis
dornase alfa
pancreatic enzyme
sweat test
tobramycin
url https://journals.lww.com/10.4103/prcm.prcm_5_20
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AT garycheok cysticfibrosisinasia
AT anneengoh cysticfibrosisinasia
AT ayehan cysticfibrosisinasia
AT sjhong cysticfibrosisinasia
AT wahyuniindawati cysticfibrosisinasia
AT armlutfulkabir cysticfibrosisinasia
AT skkabra cysticfibrosisinasia
AT harutaikamalaporn cysticfibrosisinasia
AT hyungyoungkim cysticfibrosisinasia
AT shenkunling cysticfibrosisinasia
AT sorasaklochindarat cysticfibrosisinasia
AT mohammadashkanmoslehi cysticfibrosisinasia
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AT danielng cysticfibrosisinasia
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AT rinatriasih cysticfibrosisinasia
AT zenkongdai cysticfibrosisinasia