Pediatric colorectal and pelvic reconstructive surgery / / [edited by] Marc A. Levitt, Alejandra Vilanova-Sanchez

• Pubblicazione: Boca Raton : , : CRC Press, , [2020]
• Edizione: 1st ed.
• Descrizione fisica: 1 online resource (293 pages) : illustrations
• Disciplina: 617.55059
• Soggetto topico: Pelvis - Surgery
• Persona (resp. second.): LevittMarc A <1967-> (Marc Aaron); Vilanova-SanchezAlejandra
• Note generali: Includes index.
• Nota di contenuto: Cover -- Half Title -- Title Page -- Copyright Page -- Contents -- Editors -- Contributors -- Where are we in pediatric colorectal and pelvic reconstructive surgery? New insights and the future -- 1. Pediatric colorectal and reconstructive surgery: Fundamentals of surgical preparation -- 1.1 Bowel preparation in pediatric colorectal surgery -- 1.2 Rectal enemas and rectal irrigations -- 1.3 OR setup for colorectal surgery: How to improve exposure? -- References -- 2. Basic anatomic principles of pediatric colorectal and reconstructive surgery -- 2.1 Normal anatomy of the perineum in a newborn, toddler, and adolescent -- 2.2 Technical essentials of pelvic surgery -- 2.3 Colonic vascularization and its importance in pediatric colorectal surgery -- 2.4 Sensation of the anal canal -- 2.5 Ostomy creation -- References -- 3. Anorectal malformations: The newborn period -- 3.1 VACTERL association (and syndromes) screening -- 3.2 Key anatomical findings in the newborn to identify the different types of anorectal malformations -- 3.3 How to talk with the family-Potential for bowel control: Type of malformation, sacral ratio, and spine status (the ARM continence index) -- 3.4 How to proceed when there are major co-morbidities-What should the surgeon do first? -- 3.5 Who needs a colostomy? -- References -- 4. Anorectal malformation: Definitive repair and surgical protocol -- 4.1 Preoperative considerations -- 4.2 Intraoperative considerations -- 4.3 Follow-up Long term (anal dilations) -- Selected references -- 5. Cloaca: Important steps and decision-making for pre- and post-definitive repair -- 5.1 Introduction -- 5.2 Case study -- 5.3 Postoperative care and follow-up -- References -- 6. Cloaca: Definitive repair and surgical protocol -- 6.1 Introduction -- 6.2 Case study -- 6.3 Conclusion -- References. ; 7. Long-term urologic and gynecologic follow-up in anorectal anomalies: The keys to success -- 7.1 Urologic long-term follow-up -- 7.2 Gynecologic long-term follow-up -- References -- Further reading -- 8. A patient with an anorectal malformation who has been previously repaired and who is "not doing well" -- 8.1 Case study 1 -- 8.2 Case study 2 -- 8.3 Case study 3 -- 8.4 Case study 4 -- 8.5 Case study 5 -- 8.6 Case study 6 -- References -- 9. Neonatal diagnosis of Hirschsprung disease -- 9.1 Case study -- Suggested references -- 10. Hirschsprung disease: Definitive repair with transanal pull-through -- 10.1 Case study 1 -- 10.2 Case study 2 -- 10.3 Case study 3 -- 10.4 Case study 4 -- 10.5 Transanal pull-through -- 10.6 Transanal pull-through in a child with a preliminary ostomy -- Suggested references -- 11. Total colonic Hirschsprung disease: Ileo-Duhamel -- 11.1 When to suspect TCA -- 11.2 Approach to a child struggling with washouts -- 11.3 Once the stoma is done, what is your next step in management? -- 11.4 The ileal Duhamel -- 11.5 What to do if there is an unexpected on table finding -- References -- 12. Total colonic Hirschsprung: Pre- and postoperative care -- 12.1 Ileostomy, growth, and high output: What do pediatric surgeons need to know about high output ostomy management? -- 12.2 TCHD: Hypermotility and diaper dermatitis management before and after the definitive pull-through -- 12.3 Protocol for TCHD -- 13. The post pull-through Hirschsprung patient who is not doing well with obstructive or incontinence symptoms -- 13.1 Case study 1 -- 13.2 Case study 2 -- 13.3 Case study 3 -- 13.4 Conclusions -- Further reading -- 14. Long-term outcomes of anorectal malformations and Hirschsprung disease -- 14.1 Case 1: Hirschsprung disease -- 14.2 Case 2: Hirschsprung disease -- 14.3 Case 3: Anorectal malformation in males. ; 14.4 Case 4: Anorectal malformation in females -- 14.5 Case 5: Anorectal malformation in female with a cloaca -- 14.6 Conclusions -- References -- 15. Antegrade access as an adjunct to bowel management: Appendicostomy and neoappendicostomy -- 15.1 Case study 1 -- 15.2 Case study 2 -- 15.3 Case study 3 -- 15.4 Case study 4 -- 15.5 Technical aspects for the Malone appendicostomy -- References -- 16. Severe functional constipation: Surgery and gastroenterologic collaboration -- 16.1 Introduction -- 16.2 Case study 1 -- 16.3 Case study 2 -- 16.4 Case study 3 -- 16.5 Case study 4 -- References -- 17. Colonic resection in children with colonic dysmotility -- 17.1 Case study 1 -- 17.2 Case study 2 -- 17.3 Case study 3 -- 17.4 Case study 4 -- 17.5 Case study 5 -- Further reading -- 18. Importance of collaboration in pelvic reconstruction: How to avoid complications and extra interventions -- 18.1 Case study 1 -- 18.2 Case study 2 -- 18.3 Case study 3 -- 18.4 Case study 4 -- 18.5 Overall teaching points -- References -- 19. Bowel management -- 19.1 Bowel management program -- 19.2 Case study 1 -- 19.3 Case study 2 -- 19.4 Case study 3 -- 19.5 Case study 4 -- Further reading -- 20. Evaluation of continence in children with Hirschsprung disease and anorectal malformation -- 20.1 Case study 1 -- 20.2 Case study 2 -- 20.3 Case study 3 -- 20.4 Summary (Cases 1-3) -- 20.5 Case study 4 -- 20.6 Case study 5 -- Further reading -- 21. Minor anal pathology: Rectal prolapse, perianal abscesses, hemorrhoids, anal fissures, and pilonidal disease -- 21.1 Case study 1 -- 21.2 Case study 2 -- 21.3 Case study 3 -- 21.4 Case study 4 -- 21.5 Case study 5 -- 21.6 Case study 6 -- 21.7 Case study 7 -- 21.8 Case study 8 -- References -- 22. Familial adenomatous polyposis -- 22.1 Case study 1 -- 22.2 Case study 2 -- 22.3 Case study 3 -- References. ; 23. Ulcerative colitis and indeterminate colitis in children -- 23.1 Case study 1 -- 23.2 Case study 2 -- 23.3 Case study 3 -- References -- 24. Crohn's disease in children -- 24.1 Case study 1 -- 24.2 Case study 2 -- 24.3 Case study 3 -- References -- 25. Pediatric colorectal surgery in low- and middle-income settings: Adaptation to the resources available -- 25.1 Case study 1 -- 25.2 Case study 2 -- 25.3 Case study 3 -- 25.4 Case study 4 -- 25.5 Application of general colorectal surgery principles to challenging cases prevalent in the developing world -- 25.6 Technical aspects: Performing neonatal colostomy under local anesthesia -- 25.7 Technical aspects: Periumbilical/umbilical approach as alternative to laparoscopic colonic biopsy and proximal colon mobilization for long-segment Hirschsprung disease -- 25.8 Technical aspects: Ano(recto)plasty -- 25.9 Perioperative care considerations -- 25.10 Equipment -- References -- 26. Transitional care in colorectal and pelvic reconstruction surgery -- 26.1 Case study 1 -- 26.2 Case study 2 -- 26.3 Case study 3 -- References -- 27. Operative reports of the most common procedures in pediatric colorectal surgery: Key steps -- 27.1 Laparoscopic-assisted Swenson pull-through for Hirschsprung disease -- 27.2 Open sigmoid resection for segmental colonic dysmotility -- 27.3 Laparoscopic sigmoid resection plus Malone -- 27.4 Laparoscopic Malone -- 27.5 Neoappendicostomy -- 27.6 Laparoscopic-assisted posterior sagittal anorectoplasty for anorectal malformation -- 27.7 Heineke-Mikulicz plasty for skin level stricture after anoplasty -- 27.8 PSARP recto-vestibular fistula (female) -- 27.9 PSARP perineal fistula (male) -- 27.10 Cloaca total urogenital mobilization -- 27.11 Cloaca PSARVUP: Posterior sagittal anorectovaginourethroplasty -- 27.12 Transanal Swenson pull-through for Hirschsprung disease. ; 27.13 Transanal Soave pull-through for Hirschsprung disease -- 27.14 Open Swenson for TCHD -- 27.15 Duhamel pull-through for Hirschsprung disease -- 28. Tracking operative results and outcomes -- 28.1 Case study 1 -- 28.2 Case study 2 -- 28.3 Case study 3 -- Further reading -- 29. Patient education -- 29.1 Introduction -- 29.2 Anorectal malformation -- 29.3 Hirschsprung disease -- 29.4 Bowel management -- 29.5 Surgical antegrade options -- 29.6 Urology -- References -- 30. Resources for families and the burden of therapy -- 30.1 Discussion -- 30.2 Summary -- 30.3 Case study 1 -- 31. Creating a collaborative program -- 31.1 Case 1: Starting a program -- 31.2 Case 2: Building the team -- 31.3 Case 3: Building expertise -- 31.4 Case 4: Advancing the program (iterative improvement) -- 31.5 Case 5: Data -- 31.6 Case 6: Infrastructure -- 31.7 Components of a multidisciplinary pediatric colorectal and pelvic reconstruction program -- 31.8 Steps for making the business case to the hospital -- 31.9 Components of a typical week in a current program -- References -- Index.
• Sommario/riassunto: "This book provides comprehensive coverage of the anatomical and physiological aspects of complex colorectal and pelvic malformations. Also described are the surgical protocols for this specialized field within pediatric surgery. The benefits of high- level collaboration between surgical services when treating these anomalies are explained, as are treatment algorithms and care of complications. Includes evaluation and management of the newborn Describes surgical interventions of the newborn, and when a primary repair versus a staged approach is required Explains the value of laparoscopy and deciding in which cases to use it Looks at the importance of a transition program to adulthood Pediatric surgeons worldwide and the teams in which they work will benefit from this well illustrated and comprehensive work"--
• Titolo autorizzato: Pediatric colorectal and pelvic reconstructive surgery
• ISBN: 0-429-02778-8; 0-429-63990-2
• Formato: Materiale a stampa
• Livello bibliografico: Monografia
• Lingua di pubblicazione: Inglese
• Record Nr.: 9910953209703321
• Lo trovi qui: Univ. Federico II