Literature DB >> 25482213

Newborn screening: need of the hour in India.

Ishwar C Verma1, Sunita Bijarnia-Mahay, Geetu Jhingan, Jyotsna Verma.   

Abstract

After a review of the current health scene in India, the authors suggest that the Government of India should consider seriously, the introduction of new born screening. As a first step, a central advisory committee should be constituted to recommend what is required to be done to strengthen the infrastructure and the manpower to carry out new born screening, and the disorders to be screened. In the urban hospitals newborn screening (NBS) for three disorders can be easily introduced (congenital hypothyroidism, congenital adrenal hyperplasia and G-6-PD deficiency), while in the rural areas this should begin with congenital hypothyroidism, especially in the sub Himalayan areas. Concurrently, logistic issues regarding diets and special therapies for inborn errors of metabolism should be sorted out, laboratories to confirm the diagnosis should be set up, and a cadre of metabolic physicians should be build up to treat those identified to have inborn errors of metabolism. Once these are established on a firm footing, tandem mass spectrometry should be introduced as it allows the identification of a number of disorders in an affordable manner. The recent improvements and current trends in health care in India have created the necessary infrastructure for adopting NBS for the benefit of infants in India.

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Year:  2014        PMID: 25482213     DOI: 10.1007/s12098-014-1615-0

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


  39 in total

Review 1.  Pulse oximetry screening for critical congenital heart defects in asymptomatic newborn babies: a systematic review and meta-analysis.

Authors:  Shakila Thangaratinam; Kiritrea Brown; Javier Zamora; Khalid S Khan; Andrew K Ewer
Journal:  Lancet       Date:  2012-05-02       Impact factor: 79.321

Review 2.  Newborn screening: what pediatricians should know.

Authors:  Letícia Lima Leão; Marcos José Burle de Aguiar
Journal:  J Pediatr (Rio J)       Date:  2008-08       Impact factor: 2.197

3.  Universal newborn screening for congenital hypothyroidism.

Authors:  Urvi Sanghvi; K K Diwakar
Journal:  Indian Pediatr       Date:  2008-04       Impact factor: 1.411

4.  Early identification of hearing loss and centralized newborn hearing screening facility-the Cochin experience.

Authors:  Abraham K Paul
Journal:  Indian Pediatr       Date:  2011-05       Impact factor: 1.411

5.  Efficacy of Distortion Product Oto-Acoustic Emission (OAE)/Auditory Brainstem Evoked Response (ABR) Protocols in Universal Neonatal Hearing Screening and Detecting Hearing Loss in Children <2 Years of Age.

Authors:  Girish Mishra; Yojana Sharma; Kanishk Mehta; Gunjan Patel
Journal:  Indian J Otolaryngol Head Neck Surg       Date:  2012-04-10

6.  Newborn screening in India.

Authors:  A Radha Rama Devi; S M Naushad
Journal:  Indian J Pediatr       Date:  2004-02       Impact factor: 1.967

7.  Iodine deficiency and neonatal hypothyroidism.

Authors:  N Kochupillai; C S Pandav; M M Godbole; M Mehta; M M Ahuja
Journal:  Bull World Health Organ       Date:  1986       Impact factor: 9.408

8.  Universal screening of newborns to detect hearing impairment--is it necessary?

Authors:  Narendra Rai; Neha Thakur
Journal:  Int J Pediatr Otorhinolaryngol       Date:  2013-05-01       Impact factor: 1.675

9.  Pulse oximetry screening for congenital heart defects in newborn infants (PulseOx): a test accuracy study.

Authors:  Andrew K Ewer; Lee J Middleton; Alexandra T Furmston; Abhay Bhoyar; Jane P Daniels; Shakila Thangaratinam; Jonathan J Deeks; Khalid S Khan
Journal:  Lancet       Date:  2011-08-04       Impact factor: 79.321

10.  Results from 28 years of newborn screening for congenital adrenal hyperplasia in sapporo.

Authors:  Shuntaro Morikawa; Akie Nakamura; Kaori Fujikura; Masaru Fukushi; Tomoyuki Hotsubo; Jun Miyata; Katsura Ishizu; Toshihiro Tajima
Journal:  Clin Pediatr Endocrinol       Date:  2014-04-20
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  9 in total

1.  Status of Newborn Screening and Inborn Errors of Metabolism in India.

Authors:  Seema Kapoor; B K Thelma
Journal:  Indian J Pediatr       Date:  2018-05-07       Impact factor: 1.967

2.  Newborn Screening for Congenital Hypothyroidism, Congenital Adrenal Hyperplasia, and Glucose-6-Phosphate Dehydrogenase Deficiency for Improving Health Care in India.

Authors:  Jyotsna Verma; Papai Roy; Divya C Thomas; Geetu Jhingan; Azad Singh; Sunita Bijarnia-Mahay; Ishwar C Verma
Journal:  J Pediatr Intensive Care       Date:  2019-10-14

3.  Editorial: Advances in neonatology--III.

Authors:  Dharmapuri Vidyasagar
Journal:  Indian J Pediatr       Date:  2014-12-24       Impact factor: 1.967

4.  Newborn Screening for Congenital Adrenal Hyperplasia in India: What Do We Need to Watch Out for?

Authors:  R Kishore Kumar; Hari Das; Prakash Kini
Journal:  J Obstet Gynaecol India       Date:  2015-06-11

5.  Disorders of Tetrahydrobiopterin Metabolism: Experience from South India.

Authors:  Somdattaa Ray; Hansashree Padmanabha; Vykuntaraju K Gowda; Rohan Mahale; Rita Christopher; Shruthy Sreedharan; Debjyoti Dhar; Mahesh Kamate; Madhu Nagappa; Maya Bhat; Rammurthy Anjanappa; Gautham Arunachal; M Pooja; P S Mathuranath; S R Chandra
Journal:  Metab Brain Dis       Date:  2022-01-08       Impact factor: 3.584

6.  Need and Viability of Newborn Screening Programme in India: Report from a Pilot Study.

Authors:  Arya Raveendran; Teena Joseph Chacko; Priya Prabhu; Raghava Varma; Leslie Edward Lewis; Pragna Rao; Prajna P Shetty; Yajna S Phaneendra Mallimoggala; Asha Hedge; Dinesh M Nayak; Sudeep Moorkoth; Sudheer Moorkoth
Journal:  Int J Neonatal Screen       Date:  2022-03-29

7.  Prenatal diagnosis of steroid 21-hydroxylase-deficient congenital adrenal hyperplasia: Experience from a tertiary care centre in India.

Authors:  Sudhisha Dubey; Veronique Tardy; Madhumita Roy Chowdhury; Neerja Gupta; Vandana Jain; Deepika Deka; Pankaj Sharma; Yves Morel; Madhulika Kabra
Journal:  Indian J Med Res       Date:  2017-02       Impact factor: 2.375

8.  Diversity in the incidence and spectrum of organic acidemias, fatty acid oxidation disorders, and amino acid disorders in Asian countries: Selective screening vs. expanded newborn screening.

Authors:  Naoaki Shibata; Yuki Hasegawa; Kenji Yamada; Hironori Kobayashi; Jamiyan Purevsuren; Yanling Yang; Vu Chi Dung; Nguyen Ngoc Khanh; Ishwar C Verma; Sunita Bijarnia-Mahay; Dong Hwan Lee; Dau-Ming Niu; Georg F Hoffmann; Yosuke Shigematsu; Toshiyuki Fukao; Seiji Fukuda; Takeshi Taketani; Seiji Yamaguchi
Journal:  Mol Genet Metab Rep       Date:  2018-05-21

Review 9.  Genomics of rare genetic diseases-experiences from India.

Authors:  Sridhar Sivasubbu; Vinod Scaria
Journal:  Hum Genomics       Date:  2019-09-25       Impact factor: 4.639

  9 in total

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