- Research article
- Open Access
- Open Peer Review
Chylothorax after surgery on congenital heart disease in newborns and infants -risk factors and efficacy of MCT-diet
© Biewer et al; licensee BioMed Central Ltd. 2010
- Received: 18 June 2010
- Accepted: 13 December 2010
- Published: 13 December 2010
To analyze risk factors for chylothorax in infants after congenital heart surgery and the efficacy of median chain triglyceride diet (MCT). To develop our therapeutic pathway for the management of chylothorax.
Patients and methods
Retrospective review of the institutional surgical database and patient charts including detailed perioperative informations between 1/2000 and 10/2006. Data analyzing with an elimination regression analysis.
Twenty six out of 282 patients had chylothorax (=9.2%). Secondary chest closure, low body weight, small size, longer cardiopulmonary bypass (242 ± 30 versus 129 ± 5 min) and x-clamp times (111 ± 15 versus 62 ± 3 min) were significantly associated with chylothorax (p < 0.05). One patient was cured with total parenteral nutrition (TPN) and one without any treatment. 24 patients received MCT-diet alone, which was successful in 17 patients within 10 days. After conversion to regular alimentation within one week only one chylothorax relapsed. Out of 7 patients primarily not responsive to MCT-diet, 2 were successfully treated by lysis of a caval vein thrombosis, 2 by TPN + pleurodesis + supradiaphragmatic thoracic duct ligation, one by octreotide treatment, and two patients finally died.
Chylothorax may appear due to injury of the thoracic duct, due to venous or lymphatic congestion, central vein thrombosis, or diffuse injury of mediastinal lymphatic tissue in association with secondary chest closure. Application of MCT alone was effective in 71%, and more invasive treatments like TPN should not be used in primary routine. After resolution of chylothorax, MCT-diet can be converted to regular milk formula within one week and with very low risk of relapse.
- Congenital Heart Disease
- Total Parenteral Nutrition
- Thoracic Duct
- Median Chain Triglyceride
Chylothorax is a frequent and serious complication associated with congenital heart surgery, which occurs with an incidence between 0.5% to 6.5%. It may be caused either by injury of the thoracic duct, increased pressure in the systemic veins exceeding that in the thoracic duct, or a central vein thrombosis [1–4]. The diagnosis is based on the milky or opalescent appearance of the fluid from the pleural spaces with high levels of triglycerides (> 110 mg/dl), proteins (> 20 g/L), and lymphocytes (> 80% of cells) . These large losses of nutrients and immune cells put patients at risk of malnutrition, impair their immune system and may also lead to respiratory problems with the need of a pleural drain . Published treatment strategies which aim to decrease or stop the lymphatic lymph flow are: long chain fatty acid free, median chain triglyceride (MCT)-enriched diet [2, 6, 7], total parenteral nutrition (TPN) [6, 7], octreotide therapy [2, 3, 5, 7]), optimization of hemodynamics (recanalisation of closed central veins), or closing the leakages by supraphrenic ligation or pleurodesis[8–10]. We reviewed our institutional database on congenital heart disease in a high risk population of newborns and infants for possible reasons of chylothorax and developed an algorithm for the therapeutic approach.
We carried out a systematic retrospective review of our institutional database on all surgeries of congenital heart disease in children within their first year of life at the Freiburg University Hospital between January 2000 and October 2006. Chylothorax was defined as the presence of significant pleural drainage losses with typical clinical appearance after the 5th day post op. Regularly we started milk feeding via the stomach tube as early as possible, regularly at day 3 postoperative. Therefore the typical white appearance of chylothorax was clearly observable at day 5 postoperative.
Risk factors for chylothorax
Variables used for regression analysis
age, gender, weight, height
Parameters during operation
If yes, perfusions-time, x-clamp-time, rectal temperature
The duration of sedation*, relaxation*, peritoneal dialysis, secondary chest closure
Pre-operated, re-operation, death
Group comparison was performed with the Mann-Whitney-Test (SPSS program Version 15). A p-value < 0.05 was considered to be statistically significant. The parameters (listed in Table 1) were put in a multivariate binary logistic regression analysis with backward elimination (PROC logistic, SAS Version 9). In children who received repeated surgery in the first year of life only the data of the last operation was used for investigation.
Treatment of chylothorax
On institutional consent, most patients with chylothorax were treated primarily with long chain fatty acid-free diet enriched with 1-2% MCT for at least 10 days. Additional treatment strategies were applied following clinical decision.
Characteristics of patients with chylothorax
Duration of drainage (days)
9 (3- 59)
Duration of sedation (days)
Duration of relaxation (days)
Max. loss of chyle within 24 hours (ml/kg)
43 (18 - 183)
Day of max. loss (post-op day)
Start of MCT-diet (post op-day), n = 24
Start of octreotide (post op-day); n = 3
10, 17, 20
Duration of TPN treatment (days); n = 4
6 (2 -54)
Lowest serum total protein (g/l)**, ***
Lowest serum antithrombin III (%)**
Lowest serum quick (%)**
Lowest serum immunoglobulin G (mg/dl)**
Diagnosis of the patients with chylothorax
Frequency in patients with Chylothorax
Frequency in patients without Chylothorax
Patient characteristics and operation variables
Number of patients (%)
111 ± 5.8
82.4 ± 18.9
4.8 ± 0.01
3.9 ± 0.28
58.3 ± 0.5
55.1 ± 1.4
56 (%): 44 (%)
50 (%): 50 (%)
Operations on CPB
CPB duration (min)
129 ± 4.7
242.6 ± 29.6
x-clamp time (min)
61.6 ± 2.7
110.6 ± 15.3
30.6 ± 0.31
28.7 ± 1.04
MCT-diet alone was not successful in 7 out of 24 (=29%) patients. These 7 patients had much more daily drainage losses compared to patients successfully treated with MCT-diet (median loss 119 ml/kg/day versus 40 ml/kg/day). In 4 out of these 7 patients (=57%), a subclavian, innonimate or a superior caval vein thrombosis was diagnosed. A lysis therapy in 3 out of these 4 patients was successful in reopening the vein, but resolved chylothorax only in 2. In one patient who had a contraindication for a lysis therapy, chylothorax was successfully treated with TPN and supradiaphragmatic ligation of the thoracic duct. The 2 patients with remaining chylothorax suffered from severe capillary leakage and in one of these, the thrombosis appeared. The thrombosis was secondary to chylothorax, as it had been ruled out at the beginning of treatment. This suggests that the thrombosis resulted from the massive pleural drain losses and coagulation factor imbalances. Further attempts to treat chylous pleural and abdominal effusions including TPN, octreotide treatment, supraphrenic duct ligation and pleurodesis proved unsuccessful in both these patients. Both patients suffered from severe hemodynamic problems (elevated central venous pressures, low cardiac output) and died from intensive medicine complications on day 55 and 59 respectively (= 8% of all newborns/infants with chylothorax, = 29% of the patients unresponsive to MCT-diet).
Compared to the data found in the quoted literature[1–3], our study shows a high, 9% incidence of chylothorax in the high-risk newborn and infant population. Based on our study different reasons for chylothorax may exist, i.e. surgical damage of the thoracic duct, but also damage of minor chylous vessels, as well as lymphatic congestion due to elevated central venous pressure or central vein thrombosis[2, 4, 6]. Our observation that chylothorax is associated with secondary chest closure supports the thesis that non-specific mediastinal (lymphatic) tissue damage and postoperative impaired hemodynamics should be considered as important factors in the pathophysiology of chylothorax. Chylothorax was present in 28% of the arterial switch operations (7 out of 25 patients). In contrast, chylothorax occurred only in three patients with univentricular heart after bidirectional Glenn procedure, all without evidence for highly elevated CVP. This data suggest that elevated CVP is not the major driver for chylothorax in our series.
Our study shows that 10-day treatment of chylothorax using a long chain fatty acid free MCT-enriched diet was effective in 71% of affected patients. Moreover, 90% of recovered patients tolerated well the rapid conversion  to regular alimentation (mostly breast feeding) within one week after recovery, without relapse of chylothorax (Figure 1). This is especially important for newborns and infants as the growing brain is strongly dependent on the supply of balanced fatty acid nutrition  and breast feeding encourages mother-child interaction and neurological development . Therefore we would not recommend a prophylactic administration of MCT diet after complex heart surgery without evidence of chylothorax. In contrast, TPN has much more side effects and has no higher efficacy in treating chylothorax . Panthongviriyakul and Bines suggest using TPN in cases with elevated central venous pressures >15 mmHg . When deciding over the use of TPN, its possible side-effects should be considered, such as an increased risk of nosocomial infections [13, 14]. Patients with TPN are hungry and distressed, requiring sedatives that may have a detrimental effect on blood pressure and hemodynamics, and prolong the weaning of the respirator. Patients on TPN are dependent on central venous lines, through which they receive high osmolar fluids that ensure an adequate supply of calories. This puts them at risk of developing central vein thrombosis . To avoid central lines, an oral nutrition with a low fat formula (basic-f) and intravenous application of lipids may be practical. Since central vein thrombosis has been identified as a possible cause of chylothorax, lysis treatment or an interventional procedure should be considered if a central vein thrombosis is diagnosed [16, 17]. The limitations of our study are the restricted number of patients, heterogeneous diagnoses and operations, and the retrospective design. Due to these limitations, we could not methodically analyze the impact of the loss of pro- and anti-coagulation factors, total protein and immunoglobulins on infections, thromboses and on the outcome (Table 2).
In conclusion, we found that newborns and infants who have undergone complex cardiac surgery are at the highest risk for chylothorax. These patients' risk is further increased in cases with secondary chest closure. In the majority of the patients (71% in our study), chylous leakage was temporary and could be treated effectively using a long chain fatty acid-free MCT-enriched diet, suggesting that the general use of longer and more invasive treatment is not necessary. MCT-enriched diet has no considerable negative impact on the general state of health, which is of special importance for newborns and infants and their particular nutritional requirements. Patients with persistent chylothorax carry a limited prognosis, which means that application of additional treatment strategies including surgical options should be considered in time. In particular, central vein thrombosis should be treated energetically.
- Panthongviriyakul C, Bines JE: Post-operative chylothorax in children: an evidence-based management algorithm. J Paediatr Child Health. 2008, 44 (12): 716-21. 10.1111/j.1440-1754.2008.01412.x.View ArticlePubMedGoogle Scholar
- Pratap U, Slavik Z, Ofoe VD, Onuzo O, Franklin RC: Octreotide to treat postoperative chylothorax after cardiac operations in children. Ann Thorac Surg. 2001, 72 (5): 1740-2. 10.1016/S0003-4975(01)02581-4.View ArticlePubMedGoogle Scholar
- Rosti L, De Battisti F, Butera G, Cirri S, Chessa M, Delogu A, Drago M, Giamberti A, Pome G, Carminati M, Frigiola A: Octreotide in the management of postoperative chylothorax. Pediatr Cardiol. 2005, 26 (4): 440-3. 10.1007/s00246-004-0820-4.View ArticlePubMedGoogle Scholar
- Van Veldhuizen PJ, Taylor S: Chylothorax: a complication of a left subclavian vein thrombosis. Am J Clin Oncol. 1996, 19 (2): 99-101. 10.1097/00000421-199604000-00002.View ArticlePubMedGoogle Scholar
- Roehr CC, Jung A, Proquitte H, Blankenstein O, Hammer H, Lakhoo K, Wauer RR: Somatostatin or octreotide as treatment options for chylothorax in young children: a systematic review. Intensive Care Med. 2006, 32 (5): 650-7. 10.1007/s00134-006-0114-9.View ArticlePubMedGoogle Scholar
- Al-Zubairy SA, Al-Jazairi AS: Octreotide as a therapeutic option for management of chylothorax. Ann Pharmacother. 2003, 37 (5): 679-82. 10.1345/aph.1C265.View ArticlePubMedGoogle Scholar
- Bond SJ, Guzzetta PC, Snyder ML, Randolph JG: Management of pediatric postoperative chylothorax. Ann Thorac Surg. 1993, 56 (3): 469-72. 10.1016/0003-4975(93)90881-H. discussion 472-3View ArticlePubMedGoogle Scholar
- Beghetti M, La Scala G, Belli D, Bugmann P, Kalangos A, Le Coultre C: Etiology and management of pediatric chylothorax. J Pediatr. 2000, 136 (5): 653-8. 10.1067/mpd.2000.104287.View ArticlePubMedGoogle Scholar
- Liu CS, Tsai HL, Chin TW, Wei CF: Surgical treatment of chylothorax caused by cardiothoracic surgery in children. J Chin Med Assoc. 2005, 68 (5): 234-6. 10.1016/S1726-4901(09)70214-X.View ArticlePubMedGoogle Scholar
- Pego-Fernandes PM, Jatene FB, Tokunaga CC, Simao DT, Beirutty R, Iwahashi ER, de Oliveira SA: Ligation of the thoracic duct for the treatment of chylothorax in heart diseases. Arq Bras Cardiol. 2003, 81 (3): 309-17. 10.1590/S0066-782X2003001100011.View ArticlePubMedGoogle Scholar
- Benton D: The influence of children's diet on their cognition and behavior. Eur J Nutr. 2008, 47 (Suppl 3): 25-37. 10.1007/s00394-008-3003-x.View ArticlePubMedGoogle Scholar
- Bhargava SK: Breast feeding best for the babies. Yojana. 1983, 27 (3): 29-30.PubMedGoogle Scholar
- Dhaliwal R, Heyland DK: Nutrition and infection in the intensive care unit: what does the evidence show?. Curr Opin Crit Care. 2005, 11 (5): 461-7.PubMedGoogle Scholar
- Marian M: Pediatric nutrition support. Nutr Clin Pract. 1993, 8 (5): 199-209. 10.1177/0115426593008005199.View ArticlePubMedGoogle Scholar
- Le Coultre C, Oberhansli I, Mossaz A, Bugmann P, Faidutti B, Belli DC: Postoperative chylothorax in children: differences between vascular and traumatic origin. J Pediatr Surg. 1991, 26 (5): 519-23. 10.1016/0022-3468(91)90696-Q.View ArticlePubMedGoogle Scholar
- Dittrich S, Schlensak C, Kececioglu D: Successful thrombectomy of the superior vena cava thrombosis in a newborn after cardiopulmonary bypass surgery. Interact Cardiovasc Thorac Surg. 2003, 2 (4): 692-3. 10.1016/S1569-9293(03)00209-3.View ArticlePubMedGoogle Scholar
- McCulloch MA, Conaway MR, Haizlip JA, Buck ML, Bovbjerg VE, Hoke TR: Postoperative chylothorax development is associated with increased incidence and risk profile for central venous thromboses. Pediatr Cardiol. 2008, 29 (3): 556-61. 10.1007/s00246-007-9140-9.View ArticlePubMedGoogle Scholar
- Sreeram N, Emmel M, Trieschmann U, Kruessell M, Brockmeier K, Mime LB, Bennink G: Reopening acutely occluded cavopulmonary connections in infants and children. Interact Cardiovasc Thorac Surg. 2010, 10 (3): 383-8. 10.1510/icvts.2009.226514.View ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.