Literature DB >> 20105603

Minimally invasive repair of pectus excavatum in patients with Marfan syndrome and marfanoid features.

Richard E Redlinger1, Gregory D Rushing, Alan D Moskowitz, Robert E Kelly, Donald Nuss, Ann Kuhn, Robert J Obermeyer, Michael J Goretsky.   

Abstract

PURPOSE: The presence of a pectus excavatum (PE) requiring surgical repair is a major skeletal feature of Marfan syndrome. Marfanoid patients have phenotypic findings but do not meet all diagnostic criteria. We sought to examine the clinical and management differences between Marfan syndrome patients and those who are marfanoid compared with all other patients undergoing minimally invasive PE repair.
METHODS: A retrospective institutional review board-approved review was conducted of a prospectively gathered database of all patients who underwent minimally invasive repair of PE. Patients were grouped according to diagnosis of Marfan syndrome (MAR), Marfanoid appearance (OID), and all others (ALL). Patient demographics, preoperative imaging and testing, operative strategy, complications, and postoperative surveys were evaluated. Fisher's Exact test and chi(2) were applied for statistical analysis.
RESULTS: From June 1987 to September 2008, 1192 patients underwent minimally invasive PE repair (MAR = 33, OID = 212, ALL = 947). There was a significantly higher proportion of females with either MAR or OID who underwent repair (21.5%vs 15.5%, P = .04). The MAR patients had significantly more severe PE determined by computed tomography index (MAR = 8.75, OID = 5.82, ALL = 4.94, P < .0001) and required multiple pectus bars (> or =2) to be placed during operation (MAR = 58%, OID = 36%, ALL = 29%, P = .001). There was a trend toward higher wound infection rates in MAR patients (MAR = 6%, OID = 1.4%, ALL = 1.3%, P = .07). The recurrence rate was similar among all groups (MAR = 0%, OID = 2%, ALL = 0.7%, P = .12). Successful outcome from surgeon perspective in either MAR or OID patients was similar to ALL (98%vs 98%, P = .88) and correlated well with patient satisfaction after repair (96%vs 95%, P = .43).
CONCLUSIONS: Minimally invasive PE repair is safe in patients with Marfan syndrome or marfanoid features with equally good results. Patients with Marfan syndrome have clinically more severe PE requiring multiple bars for chest repair and may have slightly higher wound infection rates. Patients are satisfied with minimally invasive repair despite a phenotypically more severe chest wall defect. Copyright 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20105603     DOI: 10.1016/j.jpedsurg.2009.10.037

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  10 in total

1.  Spinal fusion in pediatric patients with marfan syndrome: a nationwide assessment on short-term outcomes and readmission risk.

Authors:  Michael W Fields; Nathan J Lee; Jacob R Ball; Venkat Boddapati; Justin Mathew; Daniel Hong; Josephine R Coury; Zeeshan M Sardar; Benjamin Roye; Michael Vitale; Lawrence G Lenke
Journal:  Eur Spine J       Date:  2020-10-19       Impact factor: 3.134

2.  Descending aortic replacement after Nuss for pectus excavatum in a Marfan patient-Case report.

Authors:  Dawn Jaroszewski; MennatAllah Ewais; Patrick DeValeria; Michael Gotway; D Craig Miller
Journal:  Int J Surg Case Rep       Date:  2016-02-07

Review 3.  Marfan syndrome.

Authors:  Dianna M Milewicz; Alan C Braverman; Julie De Backer; Shaine A Morris; Catherine Boileau; Irene H Maumenee; Guillaume Jondeau; Arturo Evangelista; Reed E Pyeritz
Journal:  Nat Rev Dis Primers       Date:  2021-09-02       Impact factor: 65.038

4.  A young man with concurrent acute appendicitis and incarcerated right indirect inguinal hernia.

Authors:  Mohammad Farwana; Reem Farwana; Ikram Nasr
Journal:  Int Med Case Rep J       Date:  2016-04-26

5.  Efficacy of standard chest compressions in patients with Nuss bars.

Authors:  Joshua D Stearns; Jaffalie Twaibu; Dzifa Kwaku; Vincent Pizziconi; James Abbas; Ashwini Gotimukul; Dawn E Jaroszewski
Journal:  J Thorac Dis       Date:  2020-08       Impact factor: 2.895

6.  Clinical Characteristics and Thoracic factors in patients with Idiopathic and Syndromic Scoliosis Associated with Pectus Excavatum.

Authors:  Ryoji Tauchi; Yoshitaka Suzuki; Taichi Tsuji; Tetsuya Ohara; Toshiki Saito; Ayato Nohara; Kazuaki Morishita; Ippei Yamauchi; Noriaki Kawakami
Journal:  Spine Surg Relat Res       Date:  2018-01-27

Review 7.  The Musculoskeletal Manifestations of Marfan Syndrome: Diagnosis, Impact, and Management.

Authors:  Lily Pollock; Ashley Ridout; James Teh; Colin Nnadi; Dionisios Stavroulias; Alex Pitcher; Edward Blair; Paul Wordsworth; Tonia L Vincent
Journal:  Curr Rheumatol Rep       Date:  2021-11-26       Impact factor: 4.592

Review 8.  Pectus excavatum and heritable disorders of the connective tissue.

Authors:  Francesca Tocchioni; Marco Ghionzoli; Antonio Messineo; Paolo Romagnoli
Journal:  Pediatr Rep       Date:  2013-09-24

Review 9.  A scoping review presenting a wide variety of research on paediatric and adolescent patients with Marfan syndrome.

Authors:  Ingeborg Beate Lidal; Trine Bathen; Heidi Johansen; Gry Velvin
Journal:  Acta Paediatr       Date:  2020-02-17       Impact factor: 2.299

10.  Increased visceral arterial tortuosity in Marfan syndrome.

Authors:  Bence Ágg; Bálint Szilveszter; Noémi Daradics; Kálmán Benke; Roland Stengl; Márton Kolossváry; Miklós Pólos; Tamás Radovits; Péter Ferdinandy; Béla Merkely; Pál Maurovich-Horvat; Zoltán Szabolcs
Journal:  Orphanet J Rare Dis       Date:  2020-04-15       Impact factor: 4.123

  10 in total

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