TY - JOUR
T1 - Mortality from gastrointestinal congenital anomalies at 264 hospitals in 74 low-income, middle-income, and high-income countries
T2 - a multicentre, international, prospective cohort study
AU - Global PaedSurg Research Collaboration
AU - Wright, Naomi Jane
AU - Leather, Andrew J.M.
AU - Ade-Ajayi, Niyi
AU - Sevdalis, Nick
AU - Davies, Justine
AU - Poenaru, Dan
AU - Ameh, Emmanuel
AU - Ademuyiwa, Adesoji
AU - Lakhoo, Kokila
AU - Smith, Emily Rose
AU - Douiri, Abdel
AU - Elstad, Maria
AU - Sim, Marcus
AU - Riboni, Cristiana
AU - Martinez-Leo, Bruno
AU - Akhbari, Melika
AU - Tabiri, Stephen
AU - Mitul, Ashrarur
AU - Aziz, Dayang Anita Abdul
AU - Fachin, Camila
AU - Niyukuri, Alliance
AU - Arshad, Muhammad
AU - Ibrahim, Fowzia
AU - Moitt, Natalie
AU - Doheim, Mohamed Fahmy
AU - Thompson, Hannah
AU - Ubhi, Harmony
AU - Williams, Isabelle
AU - Hashim, Sophia
AU - Philipo, Godfrey Sama
AU - Herrera, Laura
AU - Yunus, Aayenah
AU - Vervoort, Dominique
AU - Parker, Samuel
AU - Benaskeur, Yousra Imane
AU - Alser, Osaid H.
AU - Adofo-Ansong, Nana
AU - Alhamid, Ahmad
AU - Salem, Hosni khairy
AU - Saleh, Mahmoud
AU - Elrais, Safa Abdal
AU - Abukhalaf, Sadi
AU - Shinondo, Patricia
AU - Nour, Ibrahim
AU - Aydin, Emrah
AU - Vaitkiene, Agota
AU - Naranjo, Kelly
AU - Dube, Andile Maqhawe
AU - Ngwenya, Sodumisa
AU - Yacoub, Mina A.
AU - Kwasau, Henang
AU - Hyman, Gabriella
AU - Elghazaly, Shrouk Mahmoud
AU - Al-Slaibi, Ibrahim
AU - Hisham, Intisar
AU - Franco, Helena
AU - Arbab, Hana
AU - Samad, Lubna
AU - Soomro, Aqil
AU - Chaudhry, Muhammad Amjad
AU - Karim, Safina
AU - Khattak, Muhammad Adnan Khan
AU - Nah, Shireen Anne
AU - Dimatatac, Doris Mae
AU - Choo, Candy SC
AU - Maistry, Niveshni
AU - Mitul, Ashrarur Rahman
AU - Hasan, Samiul
AU - Karim, Sabbir
AU - Yousuf, Hina
AU - Qureshi, Taimur
AU - Nour, Ibrahim Rabi
AU - Al-Taher, Raed Nael
AU - Sarhan, Osama Abdul Kareem
AU - Garcia-Aparicio, Luis
AU - Prat, Jordi
AU - Blazquez-Gomez, Eva
AU - Tarrado, Xavier
AU - Iriondo, Martí
AU - Bragagnini, Paolo
AU - Rite, Segundo
AU - Hagander, Lars
AU - Svensson, Emma
AU - Owusu, Sheila
AU - Abdul-Mumin, Alhassan
AU - Bagbio, Dominic
AU - Ismavel, Vijay Anand
AU - Miriam, Ann
AU - T, Shajin
AU - Anaya Dominguez, Marlene
AU - Ivanov, Monica
AU - Serban, Andreea Madalina
AU - Derbew, Miliard
AU - Elfiky, Mahmoud
AU - Olivos Perez, Maricarmen
AU - Abrunhosa Matias, Marcia
AU - Arnaud, Alexis P.
AU - Negida, Ahmed
AU - King, Sebastian
AU - Fazli, Mohamad Rafi
AU - Hamidi, Nadia
AU - Touabti, Souhem
AU - Chipalavela, Rossana Francisco
AU - Lobos, Pablo
AU - Jones, Brendan
AU - Ljuhar, Damir
AU - Singer, Georg
AU - Cordonnier, Annelien
AU - Jáuregui, Lorena
AU - Zvizdic, Zlatan
AU - Wong, Janice
AU - St-Louis, Etienne
AU - Shu, Qiang
AU - Lui, Yang
AU - Correa, Catalina
AU - Pos, Lucie
AU - Alcántara, Elvyn
AU - Féliz, Erick
AU - Zea-Salazar, Luis Enrique
AU - Ali, Liza
AU - Peycelon, Matthieu
AU - Anatole, Nzanzu Kipata
AU - Jallow, Cherno S.
AU - Lindert, Judith
AU - Ghosh, Dhruv
AU - Adhiwidjaja, Cathline Freya
AU - Tabari, Ahmad Khaleghnejad
AU - Lotfollahzadeh, Saran
AU - Mussein, Haidar Mohammad
AU - Vatta, Fabrizio
AU - Pasqua, Noemi
AU - Kihiko, David
AU - Gohil, Hetal
AU - Nour, Ibrahim R.
AU - Elhadi, Muhammed
AU - Almada, Suad Ahmed
AU - Verkauskas, Gilvydas
AU - Risteski, Toni
AU - Peñarrieta Daher, Alejandro
AU - Outani, Oumaima
AU - Hamill, James
AU - Lawal, Taiwo
AU - Mulu, Jack
AU - Yapo, Benjamin
AU - Saldaña, Lily
AU - Espineda, Beda
AU - Toczewski, Krystian
AU - Tuyishime, Eugene
AU - Ndayishimiye, Isaac
AU - Raboe, Enaam
AU - Hammond, Philip
AU - Walker, Gregor
AU - Djordjevic, Ivona
AU - Chitnis, Milind
AU - Son, Joonhyuk
AU - Lee, Sanghoon
AU - Hussien, Muaad
AU - Malik, Sawazen
AU - Ismail, Enas Musa
AU - Boonthai, Ampaipan
AU - Dahman, Nesrine Ben Hadj
AU - Hall, Nigel
AU - Castedo Camacho, Fabiola Ruth
AU - Sobrero, Helena
AU - Butler, Marilyn
AU - Makhmud, Aliev
AU - Novotny, Nathan
AU - Hammouri, Ahmad G.
AU - Al-Rayyes, Maisara
AU - Bvulani, Bruce
AU - Muraveji, Qais
AU - Murzaie, Muhammad Yousuf
AU - Sherzad, Ajmal
AU - Haidari, Sayed Aman
AU - Monawar, Abdul Baqi
AU - Samadi, Dr Ahmad Zia
AU - Thiessen, Jesh
AU - Venant, Ntakarutimana
AU - Hospital, Sonia Inamuco
AU - Jérémie, Niyonkuru
AU - Mbonicura, Jean Claude
AU - Vianney, Butoyi Jean Marie
AU - Tadesse, Amezene
AU - Negash, Samuel
AU - Roberts, Charles A.
AU - Jabang, John N.
AU - Bah, Abdoulie
AU - Camamra, Kajali
AU - Correa, Armandou
AU - Sowe, Babucarr
AU - Gai, A.
AU - Jaiteh, Musa
AU - Raymond, Kwizera Jean
AU - Mvukiyehe, Jean Paul
AU - Itangishaka, Innocent
AU - Kayibanda, Emmanuel
AU - Manirambona, Emery
AU - Lule, Joseph
AU - Costas-Chavarri, Ainhoa
AU - Alzraikat, Sayel H.
N1 - Publisher Copyright:
© 2021 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license
PY - 2021/7/24
Y1 - 2021/7/24
N2 - Background: Congenital anomalies are the fifth leading cause of mortality in children younger than 5 years globally. Many gastrointestinal congenital anomalies are fatal without timely access to neonatal surgical care, but few studies have been done on these conditions in low-income and middle-income countries (LMICs). We compared outcomes of the seven most common gastrointestinal congenital anomalies in low-income, middle-income, and high-income countries globally, and identified factors associated with mortality. Methods: We did a multicentre, international prospective cohort study of patients younger than 16 years, presenting to hospital for the first time with oesophageal atresia, congenital diaphragmatic hernia, intestinal atresia, gastroschisis, exomphalos, anorectal malformation, and Hirschsprung's disease. Recruitment was of consecutive patients for a minimum of 1 month between October, 2018, and April, 2019. We collected data on patient demographics, clinical status, interventions, and outcomes using the REDCap platform. Patients were followed up for 30 days after primary intervention, or 30 days after admission if they did not receive an intervention. The primary outcome was all-cause, in-hospital mortality for all conditions combined and each condition individually, stratified by country income status. We did a complete case analysis. Findings: We included 3849 patients with 3975 study conditions (560 with oesophageal atresia, 448 with congenital diaphragmatic hernia, 681 with intestinal atresia, 453 with gastroschisis, 325 with exomphalos, 991 with anorectal malformation, and 517 with Hirschsprung's disease) from 264 hospitals (89 in high-income countries, 166 in middle-income countries, and nine in low-income countries) in 74 countries. Of the 3849 patients, 2231 (58·0%) were male. Median gestational age at birth was 38 weeks (IQR 36–39) and median bodyweight at presentation was 2·8 kg (2·3–3·3). Mortality among all patients was 37 (39·8%) of 93 in low-income countries, 583 (20·4%) of 2860 in middle-income countries, and 50 (5·6%) of 896 in high-income countries (p<0·0001 between all country income groups). Gastroschisis had the greatest difference in mortality between country income strata (nine [90·0%] of ten in low-income countries, 97 [31·9%] of 304 in middle-income countries, and two [1·4%] of 139 in high-income countries; p≤0·0001 between all country income groups). Factors significantly associated with higher mortality for all patients combined included country income status (low-income vs high-income countries, risk ratio 2·78 [95% CI 1·88–4·11], p<0·0001; middle-income vs high-income countries, 2·11 [1·59–2·79], p<0·0001), sepsis at presentation (1·20 [1·04–1·40], p=0·016), higher American Society of Anesthesiologists (ASA) score at primary intervention (ASA 4–5 vs ASA 1–2, 1·82 [1·40–2·35], p<0·0001; ASA 3 vs ASA 1–2, 1·58, [1·30–1·92], p<0·0001]), surgical safety checklist not used (1·39 [1·02–1·90], p=0·035), and ventilation or parenteral nutrition unavailable when needed (ventilation 1·96, [1·41–2·71], p=0·0001; parenteral nutrition 1·35, [1·05–1·74], p=0·018). Administration of parenteral nutrition (0·61, [0·47–0·79], p=0·0002) and use of a peripherally inserted central catheter (0·65 [0·50–0·86], p=0·0024) or percutaneous central line (0·69 [0·48–1·00], p=0·049) were associated with lower mortality. Interpretation: Unacceptable differences in mortality exist for gastrointestinal congenital anomalies between low-income, middle-income, and high-income countries. Improving access to quality neonatal surgical care in LMICs will be vital to achieve Sustainable Development Goal 3.2 of ending preventable deaths in neonates and children younger than 5 years by 2030. Funding: Wellcome Trust.
AB - Background: Congenital anomalies are the fifth leading cause of mortality in children younger than 5 years globally. Many gastrointestinal congenital anomalies are fatal without timely access to neonatal surgical care, but few studies have been done on these conditions in low-income and middle-income countries (LMICs). We compared outcomes of the seven most common gastrointestinal congenital anomalies in low-income, middle-income, and high-income countries globally, and identified factors associated with mortality. Methods: We did a multicentre, international prospective cohort study of patients younger than 16 years, presenting to hospital for the first time with oesophageal atresia, congenital diaphragmatic hernia, intestinal atresia, gastroschisis, exomphalos, anorectal malformation, and Hirschsprung's disease. Recruitment was of consecutive patients for a minimum of 1 month between October, 2018, and April, 2019. We collected data on patient demographics, clinical status, interventions, and outcomes using the REDCap platform. Patients were followed up for 30 days after primary intervention, or 30 days after admission if they did not receive an intervention. The primary outcome was all-cause, in-hospital mortality for all conditions combined and each condition individually, stratified by country income status. We did a complete case analysis. Findings: We included 3849 patients with 3975 study conditions (560 with oesophageal atresia, 448 with congenital diaphragmatic hernia, 681 with intestinal atresia, 453 with gastroschisis, 325 with exomphalos, 991 with anorectal malformation, and 517 with Hirschsprung's disease) from 264 hospitals (89 in high-income countries, 166 in middle-income countries, and nine in low-income countries) in 74 countries. Of the 3849 patients, 2231 (58·0%) were male. Median gestational age at birth was 38 weeks (IQR 36–39) and median bodyweight at presentation was 2·8 kg (2·3–3·3). Mortality among all patients was 37 (39·8%) of 93 in low-income countries, 583 (20·4%) of 2860 in middle-income countries, and 50 (5·6%) of 896 in high-income countries (p<0·0001 between all country income groups). Gastroschisis had the greatest difference in mortality between country income strata (nine [90·0%] of ten in low-income countries, 97 [31·9%] of 304 in middle-income countries, and two [1·4%] of 139 in high-income countries; p≤0·0001 between all country income groups). Factors significantly associated with higher mortality for all patients combined included country income status (low-income vs high-income countries, risk ratio 2·78 [95% CI 1·88–4·11], p<0·0001; middle-income vs high-income countries, 2·11 [1·59–2·79], p<0·0001), sepsis at presentation (1·20 [1·04–1·40], p=0·016), higher American Society of Anesthesiologists (ASA) score at primary intervention (ASA 4–5 vs ASA 1–2, 1·82 [1·40–2·35], p<0·0001; ASA 3 vs ASA 1–2, 1·58, [1·30–1·92], p<0·0001]), surgical safety checklist not used (1·39 [1·02–1·90], p=0·035), and ventilation or parenteral nutrition unavailable when needed (ventilation 1·96, [1·41–2·71], p=0·0001; parenteral nutrition 1·35, [1·05–1·74], p=0·018). Administration of parenteral nutrition (0·61, [0·47–0·79], p=0·0002) and use of a peripherally inserted central catheter (0·65 [0·50–0·86], p=0·0024) or percutaneous central line (0·69 [0·48–1·00], p=0·049) were associated with lower mortality. Interpretation: Unacceptable differences in mortality exist for gastrointestinal congenital anomalies between low-income, middle-income, and high-income countries. Improving access to quality neonatal surgical care in LMICs will be vital to achieve Sustainable Development Goal 3.2 of ending preventable deaths in neonates and children younger than 5 years by 2030. Funding: Wellcome Trust.
UR - https://www.scopus.com/pages/publications/85110686338
U2 - 10.1016/S0140-6736(21)00767-4
DO - 10.1016/S0140-6736(21)00767-4
M3 - Article
C2 - 34270932
AN - SCOPUS:85110686338
SN - 0140-6736
VL - 398
SP - 325
EP - 339
JO - The Lancet
JF - The Lancet
IS - 10297
ER -