The ‘Re-Do’ Chest Wall Deformity By Dick G. Ellis, Charles Fort Background: A small percentage surgical correction of a chest wall so unsatisfactory that a second “re-do,” will be required. L. Snyder, Worth, of patients who undergo deformity will have results procedure, the so-called Conclusions: The literature contains very little information regarding the technique and results of these procedures. Based on experience with 18 “re-do” procedures, the authors believe that recurrent deformities should be surgically corrected. Although this is a somewhat diverse group based on S INCE 1980, we have performed reoperative chest wall surgery on 18 patients including two adult women. Twelve of the 13 boys originally had an excavaturn deformity as did four of the five girls (Table 1). Of these, we performed the original surgery on two boy excavatum patients, one boy carinatum patient, and one girl excavatum patient. Of the other 14 patients, 10 boys and 3 girls originally had an excavatum deformity, including 1 adult woman. The other patient was an adult woman who had a persistent carinatum deformity. One carinatum patient experienced recurrence as an excavaturn deformity, and in this patient, no substernal bar had been used. The patients were age 5 years to 36 years at the time of the re-do with a median of 1.5years. The patients’ ages at the time of the original surgery ranged from 35 months to 30 years with a median of 5 years. The intervals between surgeries varied from 12 months to 11 years with a median of 9 years. We only have knowledge of one boy excavatum patient of ours who underwent reoperation elsewhere. The postoperative follow-up was as short as 3 months and as long as 13 years, with a median of 1’/2 years. Six patients had follow-up for over 6 years. We have operated on 271 patients who have undergone no previous chest wall surgery, and our five recurrences represent a reoperative rate of 1.8%. Selection of patients for surgery was based entirely on the chest wall appearance and on the wishes of the patient and the family. MATERIALS Surgical AND Care ofPediatric Surgery, Vol32, Charles M. Mann Texas age at the first and second procedure, type of original operative procedure, and interval between the procedures, the operative approach is standard, and the results are predictable. J Pediatr Surg 32:1267-1271. Copyright o 1997 by W.B. Saunders Company. INDEX WORDS: carinatum. Funnel chest, pectus excavatum, pectus An attempt was made to use the old incision site and to extend it if necessary. We prefer to use a transverse incision with elevation of all soft tissue layers of the chest wall in one layer. A description of this technique is described elsewhere.’ Previous surgery has not made this particularly difficult. Intraoperatively, the deformity is again assessed. The most common finding in patients from our state, not originally operated by us, has been undisturbed deformed cartilages. The regenerated costal cartilages are usually riblike in consistency, ie, osseous, and are very adherent to the surrounding soft tissues. Robicek et al? described these findings well. There is great variability in the status of the tissue planes depending on the extent of the previous surgery. When the original procedure was limited, virginal tissue planes may be present. We feel that it is essential to remove enough of this bony tissue to allow complete mobilization of the sternum anteriorly. Bony tissue removal is performed using a Freer type periosteal elevator and a fine tipped rongeur. A curved nasal cartilage type elevator may be helpful. A thyroid tenaculum works well to grasp tissue to be elevated. If the regenerated perichondrial bundles remain taut after bony tissue removal they must be divided perpendicular to their long axis using electrocautery. This is usually on the right inferior side (Fig 1). Although sternal mobilization is essential. soft tissue connection to the sternum is preserved to the extent possible. An osteotomy of the anterior table of the sternum was used in most patients as well as a supporting substernal bar (Baxter V. Muellar, Dearfield, IL). The osteotomy is performed using a one-half inch, curved osteotome, using only enough of the tip to cut the anterior table without cutting the posterior table. Usually this is performed in the second intercostal space from left to right (Fig 2). On four occasions, two bars were used. one superiorly and one inferiorly. The bar is stainless steel, smooth, nonperforated, and non-notched3 (Fig 3). The bar is bent to the curvature of the chest wall and is passed behind the sternum through a perichondrial bed. A small parasternal opening is made on each side, and a curved tonsil hemostat, with its tip pressed against the posterior aspect of the sternum, is passed to the opposite side. The bar is grasped with this clamp and is pushed behind the sternum, following the path of the hemostat (Fig 4). The bent bar is METHODS Preoperatively, no special studies were required, although we did perform type and crossmatch tests on these patients because blood loss is greater in these cases than in primary cases. Patients were carefully instructed in deep breathing and coughing. A perioperative antibiotic, usually nafcillin, was given. We now prefer an epidural anesthetic. Journal and Correction No 9 (September), 1997: pp 1267-1271 From the Department of Surges, Cook Children i Medical Center. Fort Worth, 7X. Address reprint requests to Dr Dick Ellis. 1325 Pennsylvania Ave, Suite 670, Fort Worth, TX 76104. Copyright o 1997 by WB. Saunders Company 0022-3468/97/3209-0001$03.00/0 1267 ELLIS, 1268 Table Patient NO. 1. Clinical Characteristics Age at k-Do lyrl 15’/2 16% 36 Deformity 1 2 M F Carinatum Excavatum 30 3 F M Excavatum Excavatum 3 5 M Excavatum M F M Excavatum Carinatum Excavatum 5 8 F Excavatum M M Excavatum Excavatum M M Excavatum Excavatum M M Excavatum Excavatum M M Excavatum Excavatum 4% 5 4 M Excavatum 3% 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 Length of Follow-Up (yr) 4% 4% Excellent Good Excellent Good 1% 1 15% 1% Excellent Good Good 15% 5% 14 1% Excellent 9% 1 Excellent Excellent 1 16 17 11% 4 Result 13% 1 6 15 23 4% 7 3 MANN Excellent 13% 15% 11 20 AND and Outcome Age First Surgery (vr) Sex SNYDER, 1 12 133/i 14% 2 11% 7% 14 1 7 Good Good ‘/a Excellent Good Fair 11 passed with its concavity facing anteriorly and is then rotated 180”. The tips are placed in muscular pockets in the serratus anterior laterally with the bar resting on a rib. The bar is held in position with #l PDS sutures (Ethicon, Somerville, NJ, Z69OG) and passed around the bar and the rib. It may be possible to place three of these on each side, two around the ribs medially and laterally, and the other immediately adjacent to the sternum catching the perichondrium (Fig 5). The bar usually is passed through the fourth perichondrial bed. Once the bar is secured, additional bending is possible if needed. An F15 Jackson-Pratt drain (Baxter Medivac; McGraw Park, IL) is placed beneath the upper musculocuta- neous flap just superficial to the sternum and intercostal muscles. In several cases when the pleura was entered, a small pleural tube was placed on one or both sides and removed the next day. Fig 1. intercostal Fig 2. posterior Division of right muscles. 5th. 6th. and 7th perichondrial bundles and Complications There was one postoperative pneumothorax. A wound infection developed in two patients. One of these was localized and responded to antibiotics. The other manifested itself several weeks postoperatively and required substemal bar removal. This same patient experienced a drug overdosage, while on a patient controlled analgesia device, associated with an intravenous infusion infiltration. One patient re- Division of the table intact. anterior table of the sternum leaving the ‘RE-DO’ CHEST WALL DEFORMITY Fig 3. CORRECTION Bars and bending turned 12 years postoperatively Ulcerative colitis developed postoperatively. 1269 iron. with a broken bar. which was removed. in one teenage boy several months RESULTS Ten of the 18 patients were considered to have an excellent result based on the return of the sternum to a normal. properly oriented, anterior position (Table 1). Seven were judged to have a good result with minimal loss of correction. One boy had been previously operated on twice elsewhere and was judged to have a fair result. He regained an excellent chest wall contour after placement of a SILASTIC@ (Dow Corning, Midland, MI) implant. Nine of our 18 patients underwent transfusion, although six of the last seven did not. DISCUSSION We agree with Robicek et al? that the postoperative results of chest wall surgery cannot be measured objectively. They reported that 73 of their 608 patients ( 12%) had an “unsatisfactory” result, and of these 73, they reoperated on 42 (58%). Because there are no objective measurements, series results cannot be compared. Each Fig 4. Bar behind the elevated sternum. Fig 5. ribs. Bar secured in place behind the sternum and in front of the investigator describes the less than satisfactory results in different terms. Recurrence rates reported are 2% by Fonkalsrud? 10% by Gilbert et aL5 5% by Haller et al,6 16% by Peiia et al,’ 6% by Sanger et aLs 2.4% by Shamberger,9 and 11.8% by Singh.‘O Sixty percent of the patients who experienced recurrences in Gilbert’s5 series were over 12 years of age. Jensen et al3 reported “unsatisfactory” results in 5 of 57 patients (8X%), Golladay et al I I reoperated on 7 of 177 patients (4%), and Prevoti? also did reoperative surgery on 4% of his patients. Willital and Meierr3 saw a recurrent deformity in 20.5% of their cases if no internal supporting bar was used, but this decreased to 8.9% if the bar was used. Moghissir4 had 37% “bad” results among 54 cases. In 1970, Haller et ali5 reported 17% poor results. It seems that the incidence of recurrence is higher if the patient has Marfan’s syndrome. We have operated on eight patients who had Marfan’s syndrome and an excavatum deformity without a recurrence, but an internal metal bar support was used in all. Am et ali6 reported recurrence in 11 of 28 such patients (39%) and all of these patients underwent operation at a “young” age and without use of a bar for internal support. The reported recurrence rate is lower with carinatum deformities (Shamberger and Welch.” Robicek et al,‘* ie, in the 2% to 5% range. Age at the time of operation may be a factor in recurrence. Backer et ali9 found the results to be poorer in patients undergoing operation at a later age. FonkalsrudJ operated on his patients between ages 2 and 4, and reported a recurrence rate of only 2%. Prevot” found the ELLIS, 1270 results to be best in patients operated on between 3 and 6 years of age, and suggested that patients operated on between ages 16 and 18 years suffered the most “deterioration.” Welch20 stated that the best results were in patients undergoing operation between ages 2 and 5 years. Merge?’ recorded an increased recurrence rate if the patient was younger than 6 years or between 9 and 12 years at the time of surgery. Humphreys and Jaretzki** noted that the late results deteriorated through adolescence and were best if the patients underwent operation before age 6 years. Rehbein and Wemickez3 stated that the “late results do not always come up to expectations,” and all of their postoperative photos show residual deformities. We agree with Gilbert and Zwiren5 and others that some loss of correction often occurs during the adolescent growth spurt. Although they preferred to operate at age 4 to 5 years, 60% of the recurrences seen by Gilbert and Zwiren5 were in those patients over 12 years of age. Willital and Meier13 believe that most recurrences are seen within the first 2 or 3 years. It is interesting that Haller et alz4 recently advised against operation in patients younger than 4 years of age. They also advise against removal of five or more “ribs,” otherwise, the patients may have retarded chest wall growth and chest wall constriction. We prefer to operate on pectus excavatum patients at age 6 years if the deformity warrants surgery.25.26Excavaturn deformities do not initially have associated posterior angulation of the medial ends of the ribs. However, with time, these “secondary deformities” do develop and are not correctable. In this situation, the sternum may be returned to a normal position, but a parastemal depression may remain because of the posterior angulation of SNYDER, AND MANN the rib tips. Therefore, the surgeon must choose when to operate earlier. Carinatum deformities are virtually all operated on in the school-age period. Both Humphreys and Jaretzkiz2 and Robicek et al2 felt that the recurrence rate was related to a limited procedure at the first operation. This was strikingly obvious in three of our cases. We believe that all deformed cartilages and their contralateral partners should be subperichondrially removed, leaving a few millimeters of cartilage at the rib and sternal ends. Possibly, this will allow improved chest wall growth compared with removal of the entire length of cartilage. The remaining perichondrium will regenerate bony tissue and will even do it after a secondary procedure, although Mullard27 opposed any attempt at reoperation because of his belief that there would be no tissue that could regenerate after a secondary procedure. The re-do procedure demands methodical removal of enough regenerated cancellouslike bone to mobilize the sternum. Sometimes the perichondrial bundles are still rigid after considerable bone has been removed. Usually this is on the lower right side and we do not hesitate to divide these bundles. Although on virgin cases we avoid the retrostemal area, we will invade this area to properly mobilize the sternum. One, or even two, anterior table osteotomies may be used. A substemal bar, or even two, is a must. Our patients have toIerated this more extensive surgery very well. The results have been very pleasing. Patients who have recurrent deformities should undergo a “re-do” operation. ACKNOWLEDGMENT Appreciation is expressed to Judy Moore for secretarial assistance. REFERENCES 1. Ellis DG: Experience with a variation of the transverse incision in chest wall deformity correction, J Pediatr Surg (in press) 2. Robicek F, Daugherty HK, Mullen DC, et al: Technical considerations in the surgical management of pectus excavatum and carinatum. Ann Thorac Surg 18:549-562, 1974 3. Jensen NK, Schmidt WR, Garamella JJ, et al: Pectus excavatum and carinatum: The how, when, and why of surgical correction. J Pediatric Surg 5:4-13, 1970 4. Fonkalsrud EW: Chest wall deformities, in Bave AE, (ed): Glenn’s Thoracic and Cardiovascular Surgery. Norwalk, CT: Appleton and Lange, 1991, pp 508-514 5. Gilbert JC, Zwiren GT: Repair of pectus excavatum using a substemal metal strut within a marlex envelope. South Med J 82: 12401244,1989 6. Haller JA, Scherer LR, Turner CS, et al: Evolving management of pectus excavatum based on a single institutional experience of 664 patients. Ann Surg 209:578-583, 1989 7. Petia A, Perez L, Nurkos S, et al: Pectus carinatum and pectus excavatum: Are they the same disease?Am Surg 47:215-218, 1981 8. Sanger PW, Robicek F, Daughtery HK: The repair of recurrent pectus excavatum. J Thorac Cardiovasc Surg 56:141-142, 1968 9. Shamberger RC: in Shields TW (ed): General Thoracic Surgery. Baltimore, MD, Williams and Wilkins, 1994, pp 529-542 (chap 38) 10. Singh SV: Surgical correction of pectus excavatum and carinaturn. Thorax 35:700-702, 1980 11. Golladay ES, Wagner CW: Pectus excavatum: Perspective. South Med J 84:1099-1102, 1991 12. Prevot J: Treatment of stemocostal wall malformations of the child. A series of 210 surgical corrections since 1975. Eur J Pediatric Surg4:131-136, 1994 13. Willital GH, Meier H: Cause of funnel chest recurrencesOperative treatment and long term results. Prog Pediatr Surg 10:253255, 1977 14. Moghissi K: Long term results of surgical correction of pectus excavatum and sternal prominence. Thorax 19:350-354,1964 15. Hailer JA, Peters GN, Mazur D, et al: Pectus Excavatum: A 20 year surgical experience. J Thorac Cardiovasc Surg 60:375-381, 1970 16. Am PH, Scherer LR, Haller JA, et al: Outcome of pectus excavatum in patients with Marfan’s syndrome and in the general population. J Pediatr 115:954-958, 1989 17. Shamberger RC, Welch KJ: Surgical correction of pectus carinaturn. J Pediatr Surg 22:48-53, 1987 ‘RE-DO’ CHEST WALL DEFORMITY CORRECTION 18. Robicek F, Cook JW, Daugherty HK, et al: Pectus Carinatum. J Thorac Cardiovasc Surg 78:52-61, 1979 19. Backer OG. Brunner S, Larsen V: The surgical treatment of funnel chest. Acta Chir Scan 121:253-261, 1961 20. Welch KJ: Satisfactory surgical correction of pectus excavatum deformity in childhood. J Thorac Surg: 697-713, 1958 21. Morger R: Conservative and operative treatment of the funnel chest. Z Kinderchir 39:302-304. 1984 22. Humphreys GH, Jaretzki A: Pectus excavatum late results with and without operation. J Thorac Cardiovasc Surg 80:686-695, 1980 1271 23. Rehbein F, Wemicke HH: The operative treatment of funnel chest. Arch Dis Child 32:5-8, 1957 24. Haller JA, Colombani PM, Humphries CT, et al: Severe chest wall constriction from growth retardation after too extensive and too early pectus excavatum repair: An alert. Ann Thorac Surg 60: 1837- 1864.1995 25. Ellis DG: Chest wall deformities. Pediatr Ann 18:161-165, 1989 26. Ellis DG: Chest wall deformities. Pediatr Rev 11: 147-152, 1989 27. Mullard K: Observations on the aetiology of pectus excavatum and other chest deformities, and a method of recording them. Br J Surg 54:115-120, 1967