Mine Ün1, Oytun Erbaş2

1Istanbul Aydın University Medical Faculty, Istanbul, Turkey
2Department of Physiology, Demiroğlu Bilim University Faculty of Medicine, Istanbul, Turkey

Keywords: Intestinal failure, intestinal transplantation, solid organ transplantation

Abstract

Although intestinal transplantation has become a standard in treating intestinal failure today, it has faced significant challenges up to this point. Intestinal transplantation, which is relatively more complicated and has higher likelihood of rejection compared to other solid organ transplantations such as the liver, kidneys, and heart, has gone a long way since the 1900s and has achieved successful results.

INTESTINAL FAILURE AND ITS CAUSES

Intestinal failure is the inability of the intestines in maintaining nutrient intake and fluid balance.[1,2] Although causes of intestinal failure vary between adult and pediatric populations, one of the most important causes is short bowel syndrome (SBS) (Figure 1). Short bowel syndrome is the removal of a portion of the small intestine for any reason and the insufficiency of the remaining small intestine for the person's nutrition and survival. Short bowel syndrome, tumors, and atresia lead to intestinal failure due to intestinal loss.[2] Other causes of intestinal failure without intestinal loss are mucosal enteropathies and motility disorders.[2]

Sufficient absorption cannot occur after intestine loss. The minimum length of intestine required for sufficient absorption is not clearly defined. Various studies have proposed that the intestine must be a minimum length of 40 cm.[3,4] Intestinal length shorter than 100 cm in the first year of life is considered abnormal.[2,5-7]

Studies have reported that intestinal resection of up to 80% would be able to sustain life.[8]

INTESTINAL TRANSPLANTATION STUDIES

Excessive colonization of microorganisms in the intestine makes intestinal transplantation more difficult than other solid organs. There is greater risk for tissue rejection and sepsis.[9,10] Therefore, survival rates of recipients are also lower compared to other organ transplantations.[11,12]

Intestinal transplantation was first attempted in 1959 by Lillehei et al.[13,14] on dogs. Between 1964 and 1987, there were many interventions for transplantation of only the small intestine or both the small intestine and liver.[15] Almost all attempts resulted in sepsis and failure due to surgical problems.[16]

In 1987, clinical practices followed comprehensive studies on pig intestines.[17] One of the first clinical procedures on intestinal transplantation was performed in 1987 in Europe on a child with SBS.[18,19] From 1987 to 1990, small intestine transplantation was conducted on nine children who were administered cyclosporin in France (Cyclosporin is an oral immunosuppressive calcineurin inhibitor).[20] Only one of the nine patients had successful results.[18,19] Until 1990, only two successful results, one in France and one in Germany, were achieved.[21,22]

One of the most important causes of low success rates of transplantations during this period was the lack of developments in immunosuppressive drugs. Since the immune system was not suppressed, organ rejection developed. While success rate of intestinal transplantations was low, there have been significant developments in intestinal transplantation interventions.[18,19] The modern age of intestinal transplantation began in the 1990s in the United States.[23]

With the commercialization of tacrolimus in 1994, intestinal transplantation underwent developments worldwide.[18] Tacrolimus is an immunosuppressive drug that reduces the threat of rejection following organ transplantation.[24] Between 1994-2014, over 110 transplantations were performed in France. The annual number of intestinal transplantations is indicated below (Figure 2).[25] Of these 110 transplantations, 36 patients had SBS, 30 intestinal motility disorders, and 34 congenital enteropathies.[25] A portion of these recipients underwent transplantation of only the small intestine, while others were transplanted both small and large intestines. Additionally, nine of the recipients also received liver transplantations together with intestinal transplantation due to liver failure secondary to intestinal failure.[25]

In the first week following transplantation, recipients were fed through an enteral tube, continued with parenteral nutrition after the second week, and were allowed to be fed orally after the first month. Recipients were gradually given lactose, fiber, and proteins.[25] Within the first 10 months, intestines had to be removed in 28 recipients despite induction therapy. Ten patients underwent repeated transplantation. Only one patient achieved complete bowel functions, the others were lost due to organ rejection and sepsis.[19,26-28]

Evaluation of 101 children who underwent transplantation between 1994-2014 reported a survival rate of 33% in 2014. Deaths were due to multiorgan failure in 35% and liver failure in 50% of patients. A portion of the patients were lost due to bacterial and fungal sepsis (Enterobacter in three patients, Klebsiella in three patients, Proteus in one patient, Haemophilus in one patient and Aspergillus in two patients). Infections are a significant cause of death in these patients.[25,29-31]

WHY IS THE LIVER TRANSPLANTED TOGETHER WITH THE SMALL INTESTINE?

Patients with intestinal failure are fed with parenteral nutrition (delivery of the necessary nutrients through intravenous feeding, when nutrients cannot be fully absorbed by the intestines).[32] These patients develop liver failure due to parenteral nutrition. In this case, liver transplantation is conducted at the same time as the small intestine.[33]

VASCULAR CONNECTIONS IN INTESTINAL TRANSPLANTATION

The small intestine of the recipient is removed by cutting the Treitz ligament, revealing the veins and arteries.[16] The intestine is transplanted with anastomoses of the recipient's infrarenal aorta and the superior mesenteric artery of the donor, and the inferior vena cava of the recipient and the superior mesenteric vein of the donor. An iliac artery is inserted between the aorta and the mesenteric artery and an iliac vein between the vena cava and the mesenteric vein to facilitate anastomosis and lengthen the mesenteric vessels (Figure 3).[25,34] After vascular anastomosis is completed, it is checked whether or not blood is able to reach the organs.[16]

CAN CHRONIC REJECTION BE PREVENTED AFTER INTESTINAL TRANSPLANTATION?

Chronic rejection is the main problem in solid organ transplantations and occurs in 10% of recipients of intestinal transplantations. No pharmacological approach has proven to be effective in preventing chronic rejection. Currently, the only solution in this case is to remove the transplanted intestine.[35]

According to the results of studies and archive reports, the inclusion of liver transplantation in intestinal transplantation is the only intervention that prevents chronic rejection.[35]

Studies have found that the necessary immunosuppression for liver transplantation is relatively lower compared to other transplants. Most of the patients with long- term survival are those who have underwent intestinal transplantation accompanied by liver transplantation. Therefore, it is believed that intestinal transplantation should also include liver transplant. The “liver effect” should be benefited from to prevent rejection.[30,36-39]

HOW ARE DONORS SELECTED?

The donor’s ABO group should be the same as the recipient. Donors compatible for liver donation should also be compatible for small intestine donation. The donor should have the same or smaller size as the donor, since the volume of peritoneum cavity is usually decreased.[16]

Selective bacterial and fungal decontamination should be carried out. In other words, microorganisms in the donor should be identified and intravenous microorganism- specific antibiotic therapy should be applied to the recipient to prevent harm. Intestinal decontamination continues for at least six weeks after surgery and should be reinitiated in the periods of rejection.[16]

RECIPIENTS AFTER INTESTINAL TRANSPLANTATION

Looking back at the history of recipients 10 years after transplantations has shown many psychosocial problems including behavioral problems, developmental delay, cognitive ability disorders, school problems, anxiety, depression, and continuous reluctance to eat.[16]

Reluctance to eat is more common in children. This is because most children have never learned how to eat or have forgotten. This is why, despite lack of nutritional benefit, children are encouraged to eat before transplantation.[16]

According to studies, 46.6% of recipients attend personalized educational programs and social therapies.[40]

STATISTICAL ANALYSIS OF INTESTINAL TRANSPLANTATION

According to the 2003 report, a total of 989 transplantations were performed until that time. Reportedly, 61% of the recipients were under the age of 18.[9] Until 2003, 75.5% of the transplantations were performed in the USA, 19.1% Europe, 1.4% Asia, and 4% in Canada, South and Central America, and the Middle East.[9]

According to the 2015 report, the number of intestinal transplants since 2007 had decreased due to high morbidity and mortality of the recipients.[26,41] In 2015, The Intestinal Transplant Registry (ITR) had records of 1,697 children, in which half were still alive.[19,42]

According to the 2018 report, intestinal transplantation had undergone many developments since its start. In the last 10 years, with surgical developments, increased success in providing immunosuppression, and advancements in rehabilitation methods, there has been a significant increase in patient survival and decrease in morbidity. Patient survival has increased from 48.5% to 61.7% in the last decade (2007-2017).[40]

In conclusion, intestinal transplantation, which is relatively more complicated and has higher likelihood of rejection compared to other solid organ transplantations such as the liver, kidneys, and heart, has gone a long way since the 1900s and has achieved successful results;[43] however, multicenter studies on immunosuppression and microbiota are needed to increase the success rate and patient survival.[25]

Conflict of Interest

The authors declared no conflicts of interest with respect to the authorship and/or publication of this article.

Financial Disclosure

The authors received no financial support for the research and/or authorship of this article.

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