Skip to main content
Erschienen in: European Journal of Pediatrics 4/2024

19.01.2024 | RESEARCH

Efficacy and safety of infliximab in the treatment of Kawasaki disease: A systematic review and meta-analysis

verfasst von: Lihe Wang, Milan He, Wei Wang, Shiya Li, Guoxiao Zhao

Erschienen in: European Journal of Pediatrics | Ausgabe 4/2024

Einloggen, um Zugang zu erhalten

Abstract

Infliximab is a monoclonal antibody specifically binding tumor necrosis factor-alpha and has been approved for the treatment of several inflammatory disorders. However, the efficacy of infliximab in primary treatment of Kawasaki disease (KD) or retreatment of intravenous immunoglobulin (IVIG)-resistant KD in children is controversial. Therefore, we conducted a meta-analysis to compare the efficacy of infliximab alone or in combination with IVIG to IVIG. Eligible randomized and non-randomized trials were retrieved by searching literature databases prior to May 31, 2023. Pooled odds ratio (OR) and 95% confidence interval (95% CI) were calculated for dichotomous variables, and mean difference (MD) with 95% CI was estimated for continuous variables. A total of 14 eligible studies comprising 1257 participants were included. In refractory KD, infliximab alone was associated with a higher effectiveness rate (OR = 4.48, 95% CI 2.67–7.52) and defervescence rate (OR = 5.01, 95% CI 2.99–8.37) and resulted in a 1.08-day-shorter duration of fever (95% CI 0.61–1.55, P < 0.001) and 1.36-day-shorter length of hospital stay (95% CI 0.65–2.08) compared with IVIG. Incidences of coronary artery lesions (CALs), newly developing CALs, and CAL regression did not differ between both groups. For initial treatment of KD, infliximab in addition to IVIG led to a nominally significant higher effectiveness rate (OR = 2.26, 95% CI 1.02–5.01) and a larger reduction of right coronary artery Z score (MD = −0.24, 95% CI −0.27 to −0.21) but did not show additional efficacy in improving other outcomes. The safety profile was similar between both groups.
  Conclusion: The meta-analysis demonstrates that infliximab alone is a well-tolerated and effective treatment for IVIG-resistant KD. The additional efficacy of infliximab to IVIG for initial treatment of KD is limited. More large and high-quality trials are needed to confirm the efficacy of infliximab, especially for intensification of primary treatment for KD.
What is Known:
• Infliximab is a novel monoclonal antibody specifically blocking tumor necrosis factor-alpha and is approved for treatment of several immune-mediated inflammatory disorders.
• The efficacy of infliximab in treating children with Kawasaki disease is controversial.
What is New:
• Infliximab is an effective and safe treatment for children with refractory Kawasaki disease but adds limited efficacy to intravenous immunoglobulin for initial treatment of Kawasaki disease.
Anhänge
Nur mit Berechtigung zugänglich
Literatur
1.
Zurück zum Zitat Lin MT, Wu MH (2017) The global epidemiology of Kawasaki disease: review and future perspectives. Glob Cardiol Sci Pract 3:e201720 Lin MT, Wu MH (2017) The global epidemiology of Kawasaki disease: review and future perspectives. Glob Cardiol Sci Pract 3:e201720
2.
Zurück zum Zitat Singh S, Vignesh P, Burgner D (2015) The epidemiology of Kawasaki disease: a global update. Arch Dis Child 100(11):1084–1088PubMedCrossRef Singh S, Vignesh P, Burgner D (2015) The epidemiology of Kawasaki disease: a global update. Arch Dis Child 100(11):1084–1088PubMedCrossRef
3.
Zurück zum Zitat Daniels LB, Gordon JB, Burns JC (2012) Kawasaki disease: late cardiovascular sequelae. Curr Opin Cardiol 27(6):572–577PubMedCrossRef Daniels LB, Gordon JB, Burns JC (2012) Kawasaki disease: late cardiovascular sequelae. Curr Opin Cardiol 27(6):572–577PubMedCrossRef
4.
Zurück zum Zitat McCrindle BW, Rowley AH, Newburger JW, Burns JC, Bolger AF, Gewitz M et al (2017) Diagnosis, treatment, and long-term management of Kawasaki disease: a scientific statement for health professionals from the American Heart Association. Circulation 135(17):e927–e999PubMedCrossRef McCrindle BW, Rowley AH, Newburger JW, Burns JC, Bolger AF, Gewitz M et al (2017) Diagnosis, treatment, and long-term management of Kawasaki disease: a scientific statement for health professionals from the American Heart Association. Circulation 135(17):e927–e999PubMedCrossRef
5.
Zurück zum Zitat Newburger JW, Takahashi M, Beiser AS, Burns JC, Bastian J, Chung KJ et al (1991) A single intravenous infusion of gamma globulin as compared with four infusions in the treatment of acute Kawasaki syndrome. N Engl J Med 324(23):1633–1639PubMedCrossRef Newburger JW, Takahashi M, Beiser AS, Burns JC, Bastian J, Chung KJ et al (1991) A single intravenous infusion of gamma globulin as compared with four infusions in the treatment of acute Kawasaki syndrome. N Engl J Med 324(23):1633–1639PubMedCrossRef
6.
Zurück zum Zitat Friedman KG, Jone PN (2020) Update on the management of Kawasaki disease. Pediatr Clin North Am 67(5):811–819PubMedCrossRef Friedman KG, Jone PN (2020) Update on the management of Kawasaki disease. Pediatr Clin North Am 67(5):811–819PubMedCrossRef
7.
Zurück zum Zitat Son MB, Gauvreau K, Ma L, Baker AL, Sundel RP, Fulton DR et al (2009) Treatment of Kawasaki disease: analysis of 27 US pediatric hospitals from 2001 to 2006. Pediatrics 124(1):1–8PubMedCrossRef Son MB, Gauvreau K, Ma L, Baker AL, Sundel RP, Fulton DR et al (2009) Treatment of Kawasaki disease: analysis of 27 US pediatric hospitals from 2001 to 2006. Pediatrics 124(1):1–8PubMedCrossRef
8.
Zurück zum Zitat Moffett BS, Syblik D, Denfield S, Altman C, Tejtel-Sexson K (2015) Epidemiology of immunoglobulin resistant Kawasaki disease: results from a large, national database. Pediatr Cardiol 36(2):374–378PubMedCrossRef Moffett BS, Syblik D, Denfield S, Altman C, Tejtel-Sexson K (2015) Epidemiology of immunoglobulin resistant Kawasaki disease: results from a large, national database. Pediatr Cardiol 36(2):374–378PubMedCrossRef
9.
Zurück zum Zitat Hosoi K, Ohtsuka Y, Fujii T, Kudo T, Matsunaga N, Tomomasa T et al (2017) Treatment with infliximab for pediatric Crohn’s disease: nationwide survey of Japan. J Gastroenterol Hepatol 32(1):114–119PubMedCrossRef Hosoi K, Ohtsuka Y, Fujii T, Kudo T, Matsunaga N, Tomomasa T et al (2017) Treatment with infliximab for pediatric Crohn’s disease: nationwide survey of Japan. J Gastroenterol Hepatol 32(1):114–119PubMedCrossRef
10.
Zurück zum Zitat Rudwaleit M, Sieper J (2005) Infliximab for the treatment of ankylosing spondylitis. Expert Opin Biol Ther 5(8):1095–1109PubMedCrossRef Rudwaleit M, Sieper J (2005) Infliximab for the treatment of ankylosing spondylitis. Expert Opin Biol Ther 5(8):1095–1109PubMedCrossRef
11.
Zurück zum Zitat Ruperto N, Lovell DJ, Cuttica R, Wilkinson N, Woo P, Espada G et al (2007) A randomized, placebo-controlled trial of infliximab plus methotrexate for the treatment of polyarticular-course juvenile rheumatoid arthritis. Arthritis Rheum 56(9):3096–3106PubMedCrossRef Ruperto N, Lovell DJ, Cuttica R, Wilkinson N, Woo P, Espada G et al (2007) A randomized, placebo-controlled trial of infliximab plus methotrexate for the treatment of polyarticular-course juvenile rheumatoid arthritis. Arthritis Rheum 56(9):3096–3106PubMedCrossRef
12.
Zurück zum Zitat Furukawa S, Matsubara T, Jujoh K, Yone K, Sugawara T, Sasai K et al (1988) Peripheral blood monocyte/macrophages and serum tumor necrosis factor in Kawasaki disease. Clin Immunol Immunopathol 48(2):247–251PubMedCrossRef Furukawa S, Matsubara T, Jujoh K, Yone K, Sugawara T, Sasai K et al (1988) Peripheral blood monocyte/macrophages and serum tumor necrosis factor in Kawasaki disease. Clin Immunol Immunopathol 48(2):247–251PubMedCrossRef
13.
Zurück zum Zitat Matsubara T, Furukawa S, Yabuta K (1990) Serum levels of tumor necrosis factor, interleukin 2 receptor, and interferon-gamma in Kawasaki disease involved coronary-artery lesions. Clin Immunol Immunopathol 56(1):29–36PubMedCrossRef Matsubara T, Furukawa S, Yabuta K (1990) Serum levels of tumor necrosis factor, interleukin 2 receptor, and interferon-gamma in Kawasaki disease involved coronary-artery lesions. Clin Immunol Immunopathol 56(1):29–36PubMedCrossRef
14.
Zurück zum Zitat Burns JC, Mason WH, Hauger SB, Janai H, Bastian JF, Wohrley JD et al (2005) Infliximab treatment for refractory Kawasaki syndrome. J Pediatr 146(5):662–667PubMedCrossRef Burns JC, Mason WH, Hauger SB, Janai H, Bastian JF, Wohrley JD et al (2005) Infliximab treatment for refractory Kawasaki syndrome. J Pediatr 146(5):662–667PubMedCrossRef
15.
Zurück zum Zitat Stenbog EV, Windelborg B, Horlyck A, Herlin T (2006) The effect of TNFalpha blockade in complicated, refractory Kawasaki disease. Scand J Rheumatol 35(4):318–321PubMedCrossRef Stenbog EV, Windelborg B, Horlyck A, Herlin T (2006) The effect of TNFalpha blockade in complicated, refractory Kawasaki disease. Scand J Rheumatol 35(4):318–321PubMedCrossRef
16.
Zurück zum Zitat Weiss JE, Eberhard BA, Chowdhury D, Gottlieb BS (2004) Infliximab as a novel therapy for refractory Kawasaki disease. J Rheumatol 31(4):808–810PubMed Weiss JE, Eberhard BA, Chowdhury D, Gottlieb BS (2004) Infliximab as a novel therapy for refractory Kawasaki disease. J Rheumatol 31(4):808–810PubMed
17.
Zurück zum Zitat Zulian F, Zanon G, Martini G, Mescoli G, Milanesi O (2006) Efficacy of infliximab in long-lasting refractory Kawasaki disease. Clin Exp Rheumatol 24(4):453PubMed Zulian F, Zanon G, Martini G, Mescoli G, Milanesi O (2006) Efficacy of infliximab in long-lasting refractory Kawasaki disease. Clin Exp Rheumatol 24(4):453PubMed
18.
Zurück zum Zitat Burns JC, Best BM, Mejias A, Mahony L, Fixler DE, Jafri HS et al (2008) Infliximab treatment of intravenous immunoglobulin-resistant Kawasaki disease. J Pediatr 153(6):833–838PubMedPubMedCentralCrossRef Burns JC, Best BM, Mejias A, Mahony L, Fixler DE, Jafri HS et al (2008) Infliximab treatment of intravenous immunoglobulin-resistant Kawasaki disease. J Pediatr 153(6):833–838PubMedPubMedCentralCrossRef
19.
Zurück zum Zitat Mori M, Hara T, Kikuchi M, Shimizu H, Miyamoto T, Iwashima S et al (2018) Infliximab versus intravenous immunoglobulin for refractory Kawasaki disease: a phase 3, randomized, open-label, active-controlled, parallel-group, multicenter trial. Sci Rep 8(1):1994 Mori M, Hara T, Kikuchi M, Shimizu H, Miyamoto T, Iwashima S et al (2018) Infliximab versus intravenous immunoglobulin for refractory Kawasaki disease: a phase 3, randomized, open-label, active-controlled, parallel-group, multicenter trial. Sci Rep 8(1):1994
20.
Zurück zum Zitat Son MB, Gauvreau K, Burns JC, Corinaldesi E, Tremoulet AH, Watson VE et al (2011) Infliximab for intravenous immunoglobulin resistance in Kawasaki disease: a retrospective study. J Pediatr 158(4):644–649.e1 Son MB, Gauvreau K, Burns JC, Corinaldesi E, Tremoulet AH, Watson VE et al (2011) Infliximab for intravenous immunoglobulin resistance in Kawasaki disease: a retrospective study. J Pediatr 158(4):644–649.e1
21.
Zurück zum Zitat Youn Y, Kim J, Hong YM, Sohn S (2016) Infliximab as the first retreatment in patients with Kawasaki disease resistant to initial intravenous immunoglobulin. Pediatr Infect Dis J 35(4):457–459PubMedCrossRef Youn Y, Kim J, Hong YM, Sohn S (2016) Infliximab as the first retreatment in patients with Kawasaki disease resistant to initial intravenous immunoglobulin. Pediatr Infect Dis J 35(4):457–459PubMedCrossRef
22.
Zurück zum Zitat Han CL, Zhao SL (2018) Intravenous immunoglobulin gamma (IVIG) versus IVIG plus infliximab in young children with Kawasaki disease. Med Sci Monit 24:7264–7270PubMedPubMedCentralCrossRef Han CL, Zhao SL (2018) Intravenous immunoglobulin gamma (IVIG) versus IVIG plus infliximab in young children with Kawasaki disease. Med Sci Monit 24:7264–7270PubMedPubMedCentralCrossRef
23.
Zurück zum Zitat Tremoulet AH, Jain S, Jaggi P, Jimenez-Fernandez S, Pancheri JM, Sun X et al (2014) Infliximab for intensification of primary therapy for Kawasaki disease: a phase 3 randomised, double-blind, placebo-controlled trial. Lancet 383(9930):1731–1738PubMedCrossRef Tremoulet AH, Jain S, Jaggi P, Jimenez-Fernandez S, Pancheri JM, Sun X et al (2014) Infliximab for intensification of primary therapy for Kawasaki disease: a phase 3 randomised, double-blind, placebo-controlled trial. Lancet 383(9930):1731–1738PubMedCrossRef
24.
Zurück zum Zitat Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD et al (2021) The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ 372:n71PubMedPubMedCentralCrossRef Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD et al (2021) The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ 372:n71PubMedPubMedCentralCrossRef
25.
Zurück zum Zitat Higgins JP, Altman DG, Gotzsche PC, Juni P, Moher D, Oxman AD et al (2011) The Cochrane Collaboration’s tool for assessing risk of bias in randomised trials. BMJ 343:d5928PubMedPubMedCentralCrossRef Higgins JP, Altman DG, Gotzsche PC, Juni P, Moher D, Oxman AD et al (2011) The Cochrane Collaboration’s tool for assessing risk of bias in randomised trials. BMJ 343:d5928PubMedPubMedCentralCrossRef
26.
Zurück zum Zitat Burns JC, Roberts SC, Tremoulet AH, He F, Printz BF, Ashouri N et al (2021) Infliximab versus second intravenous immunoglobulin for treatment of resistant Kawasaki disease in the USA (KIDCARE): a randomised, multicentre comparative effectiveness trial. Lancet Child Adolesc Health 5(12):852–861PubMedCrossRef Burns JC, Roberts SC, Tremoulet AH, He F, Printz BF, Ashouri N et al (2021) Infliximab versus second intravenous immunoglobulin for treatment of resistant Kawasaki disease in the USA (KIDCARE): a randomised, multicentre comparative effectiveness trial. Lancet Child Adolesc Health 5(12):852–861PubMedCrossRef
27.
Zurück zum Zitat Dionne A, Burns JC, Dahdah N, Tremoulet AH, Gauvreau K, de Ferranti SD et al (2019) Treatment intensification in patients with Kawasaki disease and coronary aneurysm at diagnosis. Pediatrics 143(6):e20183341PubMedCrossRef Dionne A, Burns JC, Dahdah N, Tremoulet AH, Gauvreau K, de Ferranti SD et al (2019) Treatment intensification in patients with Kawasaki disease and coronary aneurysm at diagnosis. Pediatrics 143(6):e20183341PubMedCrossRef
28.
Zurück zum Zitat Jone PN, Anderson MS, Mulvahill MJ, Heizer H, Glode MP, Dominguez SR (2018) Infliximab plus intravenous immunoglobulin (IVIG) versus IVIG alone as initial therapy in children with Kawasaki disease presenting with coronary artery lesions: is dual therapy more effective? Pediatr Infect Dis J 37(10):976–980PubMedPubMedCentralCrossRef Jone PN, Anderson MS, Mulvahill MJ, Heizer H, Glode MP, Dominguez SR (2018) Infliximab plus intravenous immunoglobulin (IVIG) versus IVIG alone as initial therapy in children with Kawasaki disease presenting with coronary artery lesions: is dual therapy more effective? Pediatr Infect Dis J 37(10):976–980PubMedPubMedCentralCrossRef
29.
Zurück zum Zitat Miyata K, Bainto EV, Sun X, Jain S, Dummer KB, Burns JC et al (2023) Infliximab for intensification of primary therapy for patients with Kawasaki disease and coronary artery aneurysms at diagnosis. Arch Dis Child 108(10):833–838PubMedCrossRef Miyata K, Bainto EV, Sun X, Jain S, Dummer KB, Burns JC et al (2023) Infliximab for intensification of primary therapy for patients with Kawasaki disease and coronary artery aneurysms at diagnosis. Arch Dis Child 108(10):833–838PubMedCrossRef
30.
Zurück zum Zitat Zhang PY, Tang CZ, Chi HT, Zhang WT, Qu SQ (2018) Comparison of the effect of infliximab and intravenous immunoglobulin in the treatment of children with Kawasaki disease refractory to initial IVIG therapy. Chin J Front Med Sci 10(5):60–63 Zhang PY, Tang CZ, Chi HT, Zhang WT, Qu SQ (2018) Comparison of the effect of infliximab and intravenous immunoglobulin in the treatment of children with Kawasaki disease refractory to initial IVIG therapy. Chin J Front Med Sci 10(5):60–63
31.
Zurück zum Zitat Guo YH, Yu HG, Zhang YY, Huang N, Ma L (2020) Comparison of different treatment regimens in resistant Kawasaki disease. Chin J Rheumatol 24(7):459–462 Guo YH, Yu HG, Zhang YY, Huang N, Ma L (2020) Comparison of different treatment regimens in resistant Kawasaki disease. Chin J Rheumatol 24(7):459–462
32.
Zurück zum Zitat Peng Y, Liu XH, Ouyang Q, Duan Z (2022) Treatment of refractory Kawasaki disease with IVIG, infliximab or corticosteroids: a cohort study. Chin J Evid Based Pediatr 17(1):35–38 Peng Y, Liu XH, Ouyang Q, Duan Z (2022) Treatment of refractory Kawasaki disease with IVIG, infliximab or corticosteroids: a cohort study. Chin J Evid Based Pediatr 17(1):35–38
33.
Zurück zum Zitat Qu N, Chen Y, Dong X, Wang QN (2022) Clinical efficacy of infliximab in the treatment of immuneglobulin unresponsive Kawasaki disease. J Guangxi Med Univ 39(3):469–474 Qu N, Chen Y, Dong X, Wang QN (2022) Clinical efficacy of infliximab in the treatment of immuneglobulin unresponsive Kawasaki disease. J Guangxi Med Univ 39(3):469–474
34.
Zurück zum Zitat Cannon L, Campbell MJ, Wu EY (2023) Multisystemic inflammatory syndrome in children and Kawasaki disease: parallels in pathogenesis and treatment. Curr Allergy Asthma Rep 23(6):341–350PubMedCrossRef Cannon L, Campbell MJ, Wu EY (2023) Multisystemic inflammatory syndrome in children and Kawasaki disease: parallels in pathogenesis and treatment. Curr Allergy Asthma Rep 23(6):341–350PubMedCrossRef
35.
Zurück zum Zitat Philip S, Jindal A, Krishna Kumar R (2023) An update on understanding the pathophysiology in Kawasaki disease: possible role of immune complexes in coronary artery lesion revisited. Int J Rheum Dis 26(8):1453–1463PubMedCrossRef Philip S, Jindal A, Krishna Kumar R (2023) An update on understanding the pathophysiology in Kawasaki disease: possible role of immune complexes in coronary artery lesion revisited. Int J Rheum Dis 26(8):1453–1463PubMedCrossRef
36.
Zurück zum Zitat Ding Y, Li G, Xiong LJ, Yin W, Liu J, Liu F et al (2015) Profiles of responses of immunological factors to different subtypes of Kawasaki disease. BMC Musculoskelet Disord 16:315PubMedPubMedCentralCrossRef Ding Y, Li G, Xiong LJ, Yin W, Liu J, Liu F et al (2015) Profiles of responses of immunological factors to different subtypes of Kawasaki disease. BMC Musculoskelet Disord 16:315PubMedPubMedCentralCrossRef
37.
Zurück zum Zitat Wu Q, Weng R, Xu Y, Wang L, Huang Y, Yang J (2021) Activin a suppresses peripheral CD8(+) T lymphocyte activity in acute-phase Kawasaki disease. BMC Immunol 22(1):17PubMedPubMedCentralCrossRef Wu Q, Weng R, Xu Y, Wang L, Huang Y, Yang J (2021) Activin a suppresses peripheral CD8(+) T lymphocyte activity in acute-phase Kawasaki disease. BMC Immunol 22(1):17PubMedPubMedCentralCrossRef
40.
Zurück zum Zitat Masuda H, Kobayashi T, Hachiya A, Nakashima Y, Shimizu H, Nozawa T et al (2018) Infliximab for the treatment of refractory Kawasaki disease: a nationwide survey in Japan. J Pediatr 195(115–120):e3 Masuda H, Kobayashi T, Hachiya A, Nakashima Y, Shimizu H, Nozawa T et al (2018) Infliximab for the treatment of refractory Kawasaki disease: a nationwide survey in Japan. J Pediatr 195(115–120):e3
41.
Zurück zum Zitat Lei WT, Chang LS, Zeng BY, Tu YK, Uehara R, Matsuoka YJ et al (2022) Pharmacologic interventions for Kawasaki disease in children: a network meta-analysis of 56 randomized controlled trials. EBioMedicine 78:103946PubMedPubMedCentralCrossRef Lei WT, Chang LS, Zeng BY, Tu YK, Uehara R, Matsuoka YJ et al (2022) Pharmacologic interventions for Kawasaki disease in children: a network meta-analysis of 56 randomized controlled trials. EBioMedicine 78:103946PubMedPubMedCentralCrossRef
42.
Zurück zum Zitat Miyata K, Kaneko T, Morikawa Y, Sakakibara H, Matsushima T, Misawa M et al (2018) Efficacy and safety of intravenous immunoglobulin plus prednisolone therapy in patients with Kawasaki disease (Post RAISE): a multicentre, prospective cohort study. Lancet Child Adolesc Health 2(18):855–862PubMedCrossRef Miyata K, Kaneko T, Morikawa Y, Sakakibara H, Matsushima T, Misawa M et al (2018) Efficacy and safety of intravenous immunoglobulin plus prednisolone therapy in patients with Kawasaki disease (Post RAISE): a multicentre, prospective cohort study. Lancet Child Adolesc Health 2(18):855–862PubMedCrossRef
43.
Zurück zum Zitat Ogata S, Ogihara Y, Honda T, Kon S, Akiyama K, Ishii M (2011) Corticosteroid pulse combination therapy for refractory Kawasaki disease: a randomized trial. Padiatrics 129(1):e17–e23CrossRef Ogata S, Ogihara Y, Honda T, Kon S, Akiyama K, Ishii M (2011) Corticosteroid pulse combination therapy for refractory Kawasaki disease: a randomized trial. Padiatrics 129(1):e17–e23CrossRef
44.
Zurück zum Zitat Gambacorta A, Buonsenso D, De Rosa G, Lazzareschi I, Gatto A, Brancato F et al (2020) Resolution of giant coronary aneurisms in a child with refractory Kawasaki disease treated with anakinra. Front Pediatr 8:195PubMedPubMedCentralCrossRef Gambacorta A, Buonsenso D, De Rosa G, Lazzareschi I, Gatto A, Brancato F et al (2020) Resolution of giant coronary aneurisms in a child with refractory Kawasaki disease treated with anakinra. Front Pediatr 8:195PubMedPubMedCentralCrossRef
45.
Zurück zum Zitat Kone-Paut I, Cimaz R, Herberg J, Bates O, Carbasse A, Saulnier JP et al (2018) The use of interleukin 1 receptor antagonist (anakinra) in Kawasaki disease: a retrospective cases series. Autoimmun Rev 17(8):768–774PubMedCrossRef Kone-Paut I, Cimaz R, Herberg J, Bates O, Carbasse A, Saulnier JP et al (2018) The use of interleukin 1 receptor antagonist (anakinra) in Kawasaki disease: a retrospective cases series. Autoimmun Rev 17(8):768–774PubMedCrossRef
46.
Zurück zum Zitat Guillaume MP, Reumaux H, Dubos F (2018) Usefulness and safety of anakinra in refractory Kawasaki disease complicated by coronary artery aneurysm. Cardiol Young 28(5):739–742PubMedCrossRef Guillaume MP, Reumaux H, Dubos F (2018) Usefulness and safety of anakinra in refractory Kawasaki disease complicated by coronary artery aneurysm. Cardiol Young 28(5):739–742PubMedCrossRef
47.
Zurück zum Zitat Rajasekaran K, Duraiyarasan S, Adefuye M, Manjunatha N, Ganduri V (2022) Kawasaki disease and coronary artery involvement: a narrative review. Cureus 14(8):e28258 Rajasekaran K, Duraiyarasan S, Adefuye M, Manjunatha N, Ganduri V (2022) Kawasaki disease and coronary artery involvement: a narrative review. Cureus 14(8):e28258
Metadaten
Titel
Efficacy and safety of infliximab in the treatment of Kawasaki disease: A systematic review and meta-analysis
verfasst von
Lihe Wang
Milan He
Wei Wang
Shiya Li
Guoxiao Zhao
Publikationsdatum
19.01.2024
Verlag
Springer Berlin Heidelberg
Erschienen in
European Journal of Pediatrics / Ausgabe 4/2024
Print ISSN: 0340-6199
Elektronische ISSN: 1432-1076
DOI
https://doi.org/10.1007/s00431-024-05437-2

Weitere Artikel der Ausgabe 4/2024

European Journal of Pediatrics 4/2024 Zur Ausgabe

Neuer Typ-1-Diabetes bei Kindern am Wochenende eher übersehen

23.04.2024 Typ-1-Diabetes Nachrichten

Wenn Kinder an Werktagen zum Arzt gehen, werden neu auftretender Typ-1-Diabetes und diabetische Ketoazidosen häufiger erkannt als bei Arztbesuchen an Wochenenden oder Feiertagen.

Neue Studienergebnisse zur Myopiekontrolle mit Atropin

22.04.2024 Fehlsichtigkeit Nachrichten

Augentropfen mit niedrig dosiertem Atropin können helfen, das Fortschreiten einer Kurzsichtigkeit bei Kindern zumindest zu verlangsamen, wie die Ergebnisse einer aktuellen Studie mit verschiedenen Dosierungen zeigen.

Spinale Muskelatrophie: Neugeborenen-Screening lohnt sich

18.04.2024 Spinale Muskelatrophien Nachrichten

Seit 2021 ist die Untersuchung auf spinale Muskelatrophie Teil des Neugeborenen-Screenings in Deutschland. Eine Studie liefert weitere Evidenz für den Nutzen der Maßnahme.

Fünf Dinge, die im Kindernotfall besser zu unterlassen sind

18.04.2024 Pädiatrische Notfallmedizin Nachrichten

Im Choosing-Wisely-Programm, das für die deutsche Initiative „Klug entscheiden“ Pate gestanden hat, sind erstmals Empfehlungen zum Umgang mit Notfällen von Kindern erschienen. Fünf Dinge gilt es demnach zu vermeiden.

Update Pädiatrie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.