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Article

Benefits of Paediatric to Adult Transition Programme in Inflammatory Bowel Disease: The BUTTERFLY Study of GETECCU and SEGHNP

by
Cristina Rubín de Célix
1,*,
Javier Martín-de-Carpi
2,
Gemma Pujol-Muncunill
2,
Laura María Palomino
3,
Marta Velasco Rodríguez-Belvís
3,
Rafael Martín-Masot
4,
Víctor Manuel Navas-López
4,
Elena Ricart
5,
María José Casanova
1,
Alejandro Rodríguez-Martínez
6,
Eduardo Leo-Carnerero
7,
Alba Alcaraz
8,
Miriam Mañosa
9,
Vicent Hernández
10,
María Consuelo Cobelas Cobelas
11,
César Sánchez
12,
Luis Menchén
13,
Francisco Mesonero
14,
Manuel Barreiro-De Acosta
15,
Nazareth Martinón-Torres
16,
Coral Tejido Sandoval
17,
Alicia Rendo Vázquez
18,
Pilar Corsino
19,
Raquel Vicente
19,
Alejandro Hernández-Camba
20,
José Ramón Alberto Alonso
21,
I. Alonso-Abreu
22,
Ana María Castro Millán
23,
Laia Peries Reverter
24,
Beatriz Castro
25,
Estela Fernández-Salgado
26,
M. Mercedes Busto Cuiñas
27,
José Manuel Benítez
28,
Lucía Madero
29,
Fernando Clemente
30,
Sabino Riestra
31,
Santiago Jiménez-Treviño
32,
Maia Boscá-Watts
33,
Elena Crehuá-Gaudiza
34,
Marta Calvo Moya
35,
José María Huguet
36,
Ester-María Largo-Blanco
37,
Leticia González Vives
38,
Rocío Plaza
39,
Iván Guerra
40,
Josefa Barrio
41,
Laura Escartín
42,
Erika Alfambra
43,
Noelia Cruz
44,
M. Carmen Muñoz
45,
María Guadalupe Muñoz Pino
46,
Manuel Van Domselaar
47,
Belén Botella
48,
David Monfort Miquel
49,
M. Carmen Rodríguez Grau
50,
Agustín De La Mano
51,
Yolanda Ber
52,
María Calvo Iñiguez
53,
Teresa de Jesús Martínez-Pérez
54,
María Chaparro
1,† and
Javier P. Gisbert
1,†add Show full author list remove Hide full author list
1
Gastroenterology Department, Hospital Universitario de La Princesa, Instituto de Investigación Sanitaria Princesa (IIS-Princesa), Universidad Autónoma de Madrid (UAM), Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), 28006 Madrid, Spain
2
Department of Paediatric Gastroenterology, Hepatology and Nutrition, Hospital Sant Joan de Déu, 08950 Barcelona, Spain
3
Paediatric Gastroenterology and Nutrition Department, Hospital Infantil Universitario Niño Jesús, 28009 Madrid, Spain
4
Paediatric Gastroenterology and Nutrition Unit, Hospital Regional Universitario de Málaga, Biomedical Re-search Institute of Málaga (IBIMA), 29010 Málaga, Spain
5
Gastroenterology Department, Hospital Clínic, Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), Institut d’Investigacions Biomèdiques Agustí Pi i Sunyer (IDIBAPS), 08036 Barcelona, Spain
6
Paediatric Gastroenterology, Hepatology and Nutrition, UGC de Pediatría, Hospital Universitario Virgen del Rocío, 41013 Sevilla, Spain
7
Gastroenterology Department, Hospital Virgen del Rocío, 41013 Sevilla, Spain
8
Department of Paediatric Gastroenterology, Nutrition and Hepatology, University Hospital Germans Trias I Pujol, 08916 Badalona, Spain
9
Gastroenterology Department, Hospital Universitari Germans Trias I Pujol, Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), 08916 Badalona, Spain
10
Department of Gastroenterology, Xerencia Xestion Integrada de Vigo, SERGAS, Research Group in Digestive Diseases, Galicia Sur Health Research Institute (IIS Galicia Sur), SERGAS-UVIGO, 36312 Vigo, Spain
11
Department of Paediatrics, Xerencia Xestion Integrada de Vigo, SERGAS, 36312 Vigo, Spain
12
Paediatric Gastroenterology, Hepatology and Nutrition Department, Hospital General Universitario Gregorio Marañón, 28018 Madrid, Spain
13
Gastroenterology Department–CEIMI, Hospital General Universitario Gregorio Marañón, Departamento de Medicina, Universidad Complutense de Madrid, 28018 Madrid, Spain
14
Gastroenterology Department, Hospital Universitario Ramón y Cajal, 28034 Madrid, Spain
15
Gastroenterology Department, Hospital Universitario Clínico de Santiago, 15706 Santiago de Compostela, Spain
16
Paediatric Gastroenterology, Hepatology and Nutrition Unit, Hospital Universitario Clínico de Santiago, 15706 Santiago de Compostela, Spain
17
Gastroenterology Department, Complejo Hospitalario Universitario de Ourense, 32005 Orense, Spain
18
Paediatric Gastroenterology, Hepatology and Nutrition Unit, Complejo Hospitalario Universitario de Ourense, 32005 Orense, Spain
19
Inflammatory Bowel Disease Unit, Gastroenterology Department, Hospital Universitario Miguel Servet, Health Research Institute of Aragón, 50009 Zaragoza, Spain
20
Gastroenterology Department, Hospital Universitario Nuestra Señora de Candelaria, 38010 Santa Cruz de Tenerife, Spain
21
Paediatric Gastroenterology, Hepatology and Nutrition Unit, Hospital Universitario Nuestra Señora de Candelaria, 38010 Santa Cruz de Tenerife, Spain
22
Gastroenterology Department, Hospital Universitario de Canarias, 38320 Santa Cruz de Tenerife, Spain
23
Paediatric Gastroenterology, Hepatology and Nutrition Unit, Hospital Universitario de Canarias, 38320 Santa Cruz de Tenerife, Spain
24
Gastroenterology Department, Hospital Universitari de Girona Doctor Josep Trueta, 17007 Girona, Spain
25
Gastroenterology Department, Hospital Universitario Marqués de Valdecilla, 39008 Santander, Spain
26
Gastroenterology Department, Complejo Hospitalario Universitario de Pontevedra, 36071 Pontevedra, Spain
27
Paediatric Gastroenterology, Hepatology and Nutrition Unit, Complejo Hospitalario Universitario de Pontevedra, 36071 Pontevedra, Spain
28
Gastroenterology Department, Hospital Universitario Reina Sofía, IMIBIC, 14004 Córdoba, Spain
29
Gastroenterology Department, Hospital Universitario de Alicante, Instituto de Investigación Sanitaria y Biomedica (ISABIAL), 03010 Alicante, Spain
30
Paediatric Gastroenterology, Hepatology and Nutrition Unit, Hospital Universitario de Alicante, 03010 Alicante, Spain
31
Gastroenterology Department, Hospital Universitario Central de Asturias, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), 33011 Oviedo, Spain
32
Paediatric Gastroenterology and Nutrition Unit, Hospital Universitario Central de Asturias, 33011 Oviedo, Spain
33
Gastroenterology Department, Hospital Clínico de Valencia, 46010 Valencia, Spain
34
Paediatric Gastroenterology, Hepatology and Nutrition Unit, Hospital Clínico de Valencia, 46010 Valencia, Spain
35
Inflammatory Bowel Disease Unit, Department of Gastroenterology and Hepatology, Hospital Puerta de Hierro, 28222 Madrid, Spain
36
Gastroenterology Department, Consorcio Hospital General Universitario de Valencia, 46014 Valencia, Spain
37
Paediatric Gastroenterology, Hepatology and Nutrition Unit, Consorcio Hospital General Universitario de Valencia, 46014 Valencia, Spain
38
Gastroenterology, Hepatology and Nutrition Unit, Hospital Universitario Infanta Leonor, 28031 Madrid, Spain
39
Gastroenterology Department, Hospital Universitario Infanta Leonor, 28031 Madrid, Spain
40
Gastroenterology Department, Hospital Universitario de Fuenlabrada, 28942 Madrid, Spain
41
Paediatric Gastroenterology Unit, Hospital Universitario de Fuenlabrada, 28942 Madrid, Spain
42
Paediatric Gastroenterology, Hepatology and Nutrition Unit, Hospital Clínico Universitario Lozano Blesa, 50009 Zaragoza, Spain
43
Gastroenterology Department, Hospital Clínico Universitario Lozano Blesa, 50009 Zaragoza, Spain
44
Gastroenterology Department, Hospital Doctor José Molina Orosa, 35500 Las Palmas, Spain
45
Gastroenterology Department, Hospital Universitario de Basurto, 48013 Bilbao, Spain
46
Paediatric Gastroenterology, Hepatology and Nutrition Unit, Hospital de Torrejón, 28850 Madrid, Spain
47
Gastroenterology Department, Hospital de Torrejón, 28850 Madrid, Spain
48
Gastroenterology Department, Hospital Universitario Infanta Cristina, 28981 Madrid, Spain
49
Gastroenterology Department, Centro Consorci Sanitari Terrassa, 08227 Terrassa, Spain
50
Gastroenterology Department, Hospital de Henares, 28822 Madrid, Spain
51
Paediatric Gastroenterology, Hepatology and Nutrition Unit, Hospital de Henares, 28822 Madrid, Spain
52
Gastroenterology Department, Hospital de San Jorge, 22004 Huesca, Spain
53
Gastroenterology Department, Hospital San Pedro, 28037 La Rioja, Spain
54
Gastroenterology Department, Hospital Virgen de La Luz, 16002 Cuenca, Spain
 
add Show full affiliation list
 
remove Hide full affiliation list
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
J. Clin. Med. 2023, 12(14), 4813; https://doi.org/10.3390/jcm12144813
Submission received: 15 May 2023 / Revised: 10 July 2023 / Accepted: 14 July 2023 / Published: 21 July 2023
(This article belongs to the Special Issue Clinical Advances in Inflammatory Bowel Disease)
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Versions Notes

Abstract

:
(1) Background: Transition is a planned movement of paediatric patients to adult healthcare systems, and its implementation is not yet established in all inflammatory bowel disease (IBD) units. The aim of the study was to evaluate the impact of transition on IBD outcomes. (2) Methods: Multicentre, retrospective and observational study of IBD paediatric patients transferred to an adult IBD unit between 2017–2020. Two groups were compared: transition (≥1 joint visit involving the gastroenterologist, the paediatrician, a programme coordinator, the parents and the patient) and no-transition. Outcomes within one year after transfer were analysed. The main variable was poor clinical outcome (IBD flare, hospitalisation, surgery or any change in the treatment because of a flare). Predictive factors of poor clinical outcome were identified with multivariable analysis. (3) Results: A total of 278 patients from 34 Spanish hospitals were included. One hundred eighty-five patients (67%) from twenty-two hospitals (65%) performed a structured transition. Eighty-nine patients had poor clinical outcome at one year after transfer: 27% in the transition and 43% in the no-transition group (p = 0.005). One year after transfer, no-transition patients were more likely to have a flare (36% vs. 22%; p = 0.018) and reported more hospitalisations (10% vs. 3%; p = 0.025). The lack of transition, as well as parameters at transfer, including IBD activity, body mass index < 18.5 and corticosteroid treatment, were associated with poor clinical outcome. One patient in the transition group (0.4%) was lost to follow-up. (4) Conclusion: Transition care programmes improve patients’ outcomes after the transfer from paediatric to adult IBD units. Active IBD at transfer impairs outcomes.

1. Introduction

Transition is defined as the intentional and planned movement of adolescents and young adults with chronic medical conditions from children to adult-oriented healthcare systems [1]. In Europe, up to 25% of the patients with inflammatory bowel disease (IBD) are diagnosed at a paediatric age, and a growing incidence of paediatric IBD has been reported [2,3,4].
Transition is a complex, structured and dynamic process in which the patient, the parents, the gastroenterologist and the paediatrician must be involved. The agents involved in this process may have different perspectives regarding the management of the disease, and the transition programme allows identification and solution of these differences [5].
During the transition, it is essential to guarantee the continuity of medical assistance from paediatric to adult IBD units [6]. Recently, some clinical practice guidelines and consensus recommendations on transition in IBD have been published [5,7,8,9,10]. However, the majority of their recommendations are based mainly on scientific evidence deemed as “weak” due to the limited number of patients included in the studies and the difficulty of finding an appropriate definition for a “successful transition” [5,7,11]. Regarding this topic, some possible transition models have been proposed [5] and, although there is no evidence suggesting that one model is superior to the others, there is a consensus on the fact that there should be a transition process in chronic diseases, particularly in IBD. Despite certain evidence of the usefulness of the transition programmes in IBD [12,13], their implementation is not yet established in all the paediatric and adult IBD units.
We therefore designed a multicentre and collaborative study between paediatric gastroenterologists and adult gastroenterologists in order to assess the benefit of transition programmes in a real-world setting. The aim of our study was to evaluate the benefit of a planned and structured transition programme for the transfer of IBD patients from paediatric to adult IBD units. We also aimed to assess the prevalence and the different subtypes of transition programmes in Spain and to identify the possible predictive factors of poor clinical outcome and loss to follow-up after the transfer.

2. Materials and Methods

2.1. Study Design and Selection of Participating Centres

A retrospective, multicentre, noninterventional study was carried out in Spain. IBD units that had identified referral paediatricians and accepted to participate in the project were included. Centres with structured transition and others in which the transition programme was not implemented (and patients were just transferred from the paediatric to the adult IBD unit) were included and served as comparators.
The project was assessed by a scientific committee, involving experienced paediatricians on transition in IBD and leaders of the Spanish Society for Paediatric Gastroenterology, Hepatology and Nutrition (SEGHNP). The Spanish Group on Crohn’s Disease and Ulcerative Colitis (GETECCU) evaluated and accepted the study protocol. The study was conducted according to the ethical principles of the Declaration of Helsinki. The study protocol was approved by the Drug Research Ethics Committee (Comité de Ética de la Investigación con Medicamentos) at the Hospital Universitario de La Princesa in Madrid, Spain.

2.2. Patient Population

IBD patients diagnosed according to the Porto criteria of the European Society for Paediatric Gastroenterology Hepatology and Nutrition (ESPGHAN) [14] who were transferred from the paediatric to the adult IBD unit from March 2017 to March 2020 were included. Patients with less than one year of follow-up in paediatric care and IBD patients transferred by a different route than the referral paediatric gastroenterologist of the adult IBD unit were excluded. Patients were analysed in two groups depending on whether or not they had undergone a structured transition.

2.3. Study Outcomes

The primary outcome was poor clinical outcome, defined as any (at least one) of the following events: (1) Need for hospitalisation due to an IBD flare; (2) Need for surgery due to IBD activity or complications of the IBD; and (3) IBD recurrence/flare-up that required a change in treatment (either intensification of the treatment or change to a different drug and addition of another therapy). The change in the treatment planned by the IBD team during the joint visits and performed immediately after transfer (in the first visit with the adult gastroenterologist) was not considered as a poor clinical outcome.

2.4. Data Collection

All clinical data were extracted from the medical records of each participating hospital. Paediatric gastroenterologists identified the patients who finished the follow-up in paediatric care in their medical records (because they had reached the age to be referred to the adult IBD unit) and verified if the patients met the inclusion criteria. The paediatric gastroenterologist also completed the IBD information for each patient until the date of discharge from paediatric care. The adult gastroenterologist included the information of the variables of interest during the first year after the transfer from the paediatric clinic and detected the patients who were lost to follow-up. Moreover, the gastroenterologist identified in their medical records which patients should have been transferred from the referring paediatric gastroenterologist.
The following clinical variables were included in the study: sex, age at IBD diagnosis, smoking history, family history of IBD, disease extension according to the Paris classification [15], presence of perianal disease, psychiatric comorbidities, extraintestinal manifestations (EIMs) and immune-mediated diseases, medical treatments received (exclusive enteral nutrition (EEN), aminosalicylates, corticosteroids, immunomodulators and biologic drugs) and surgical procedures due to an IBD flare or IBD complication. We compiled information from the radiological examinations (magnetic resonance enterography (MRE) and abdominal ultrasound), endoscopic evaluation and biologic markers (albumin, C-reactive protein or faecal calprotectin) when available. We also collected data about the transition programme: starting date, transition place, number of joint visits, transition duration and the professionals involved in the transition. Patients were followed-up until 12 months after transfer.
Study data were collected and managed using the Research Electronic Data Capture (REDCap) electronic data capture tools hosted by the Spanish Gastroenterology Association (AEG). REDCap is a secure, web-based software platform designed to support data capture for research studies, providing (1) an intuitive interface for validated data capture; (2) audit trails for tracking data manipulation and export procedures; (3) automated export procedures for seamless data downloads to common statistical packages; and (4) procedures for data integration and interoperability with external sources [16,17]. Data were remotely monitored to assess data quality.

2.5. Definitions

2.5.1. Transition-Related Definitions

  • Transition: Intentional and planned movement of adolescents and young adults suffering from chronic physical and medical conditions from child- to adult-oriented healthcare systems. We defined transition as a structured process involving the gastroenterologist, the paediatrician and a programme coordinator, as well as the parents and the IBD patient. At least one joint visit should have been carried out by those involved in the transition process.
  • Transfer: Moment at which the medical attention was carried out by the gastroenterologist. We defined the transfer as the date of discharge from the paediatric clinic.

2.5.2. Clinical Definitions

  • Type of hospital: Hospitals were clustered in conglomerates, taking into account different variables such as provision, offer of services, activity, complexity or teaching, which established the following three categories: (1) first-level hospital (less than 150 beds on average, hardly any high-tech resource and low complexity); (2) second-level hospital (of average size around 500 beds, medium complexity and some teaching activity); and (3) third-level hospital (large referral hospitals with great structural weight, full offer of services, great teaching and assistance activity and high complexity).
  • Smoking status: Patients were considered “smokers” if they smoked more than seven cigarettes per week for at least six months and had smoked at least one cigarette in the six months prior to transfer. Patients were considered “ex-smokers” if they quit smoking at least six months before transfer. Patients were considered “non-smokers” if they never smoked or did so in very small amounts or occasionally. The smoking status was also categorised 12 months after transfer [18].
  • IBD location and phenotype were defined according to the Paris classification [15].
  • IBD activity: The Harvey–Bradshaw Index (HBI) [19] for Crohn’s disease (CD) and the partial Mayo score [20] for ulcerative colitis (UC) were used in the gastroenterologist setting. On the other hand, the Paediatric CD Activity Index (PCDAI) or the weighted PCDAI (wPCDAI) for CD [21] and the Paediatric UC Activity Index (PUCAI) [22] for UC were used in the paediatric setting. When endoscopy or radiological examination was available, the severity was graded as quiescent, mild, moderate or severe by local investigators.
  • Biologic markers: Levels of C-reactive protein and faecal calprotectin were considered as high when >0.5 mg/dL and >250 µg/g, respectively.
  • Patients lost to follow-up were defined as those who did not attend the gastroenterology unit during 12 months after transfer.

2.6. Statistical Analysis

Patient’s characteristics were analysed according to the presence or absence of a structured transition programme. For categorical variables, percent values and their 95% confidence intervals (CIs) were calculated. For continuous variables, arithmetic mean and the standard deviation, or the median and the interquartile range (IQR), were calculated depending on whether or not they were normally distributed. Categorical variables were compared using the chi-square test (χ2) and quantitative variables using the appropriate test (Student’s t and Wilcoxon) depending on whether their values followed a normal distribution or not.
Poor clinical outcome was established as a dependent variable. Independent variables were those that achieved statistical significance in the univariate study or those that were clinically relevant. Variables associated with poor clinical outcome were analysed by the Kaplan–Meier method, in which patients were censored at the time of poor clinical outcome for any reason. Any differences between survival curves were evaluated using the log-rank test. Stepwise multivariable analysis using the Cox regression model was used to investigate factors potentially associated with poor clinical outcome. Patients lost to follow-up were included in the statistical analysis. A subanalysis was carried out exclusively including patients undergoing transition and who were in remission at the time of transfer to the adult IBD unit. In the log-rank test and in the multivariable analysis, p values of <0.05 were considered as statistically significant.

3. Results

3.1. Patient Population

A total of 278 patients met the inclusion criteria and were included. Overall, 185 (67%; 95% CI = 61–72) underwent a structured transition and 93 (33%; 95% CI = 28–39) were just transferred from the paediatric to the adult IBD unit (Figure 1).
Patient demographics and baseline characteristics are summarised in Table 1. Family history of IBD and psychiatric comorbidity were more commonly reported in the transition group. Median age at diagnosis was 12 years in both groups, and approximately 60% of the patients were male. Median disease duration at transfer were 54 and 51 months in the transition and in the no-transition group, respectively. In the transition group, 57% of the patients had CD (vs. 56% of the patients in the no-transition group). The majority of CD patients had ileocolonic involvement, and inflammatory behaviour was the most common one (Table 1).

3.2. Characteristics of the Participating Hospitals

A total of 34 centres participated in the study. Overall, 22 (65%; 95% CI = 48–78) centres performed a structured transition, and in 12 (35%; 95% CI = 21–52), the transition programme was not implemented. The majority of the centres with an implemented transition programme were large hospitals with medical doctors focused on IBD. Paediatric and gastroenterology IBD units were predominant in the transition group (62% vs. 8%, p = 0.001 and 100% vs. 67%, p = 0.004, respectively). The mean number of joint visits during transition were 1.5, and the mean duration of the transition was approximately six months. The IBD nurse was involved in the transition programme in 62% of the cases. Characteristics of the participating hospitals are summarised in Table 2.

3.3. Clinical Outcomes

Of the 278 patients included, 89 (32%; 95% CI = 27–38) had a poor clinical outcome within one year after transfer: 49/185 (27%; 95% CI = 21–33) in the transition group and 40/93 (43%; 95% CI = 33–53) in the no-transition cohort (p = 0.005). The median time for a poor clinical outcome was 9.3 months (95% CI = 8–10) in the no-transition group and 10.4 months (95%CI 10–11) in the transition cohort (p > 0.05).
Regarding outcomes before transfer, prior emergency visits were reported in 47% of the patients in the no-transition group vs. 31% of the patients in the transition cohort (p = 0.007). In total, 47% of the patients in the transition group needed hospitalisation vs. 42% of the patients in the no-transition cohort (p > 0.05), and corticosteroid treatment was reported in 59% in the no-transition cohort vs. 49% in the transition group (p > 0.05). Approximately 80% of patients had received immunosuppressants, and half of the patients had needed biologic drugs (54% in the transition group vs. 41% in the no-transition cohort, p = 0.038) (Table 3).
Within one year after transfer, 36% of the patients in the no-transition group had an IBD flare, requiring intensification of the treatment or change to another drug (p = 0.018). Emergency visits were reported in 17% of the patients in the no-transition group vs. 10% in the transition cohort (p > 0.05). Ten percent of the patients in the no-transition group needed a hospitalisation vs. three percent in the transition cohort (p = 0.025). Use of corticosteroids was reported in 15% of the patients in the no-transition group vs. 9% in the transition cohort (p = 0.002). The outcomes of interest were not affected by the presence or absence of a paediatric or gastroenterology IBD unit (Table 3).
In eight patients, the paediatric gastroenterologist and the adult gastroenterologist agreed on an elective change in the treatment that was carried out immediately after the transfer: six patients (75%) in the transition group and two patients (25%) in the no-transition cohort. The changes in the treatment for the IBD were that four patients started a new drug, two patients modified the dose of the treatment received, one patient stopped the treatment for IBD and one patient modified and stopped the treatment during the follow-up. All these changes were not considered as poor clinical outcome in our study.
Regarding the patients in remission, 150 patients (81%) in the transition group and 75 patients (81%) in the no-transition cohort had quiescent disease at their first referral to the adult IBD unit (p > 0.05). Regarding the transitioned patients in remission, 28 patients (19%; 95% CI = 13–26) had a poor clinical outcome during the follow-up: 2 patients (1%) required surgery, 2 patients (1%) were hospitalised due to an IBD flare and 26 patients (17%) needed a change in the treatment because of a flare of the disease. On the other hand, 24 patients in the no-transition group in clinical remission at transfer (32%; 95% CI = 23–43) had a poor clinical outcome during the follow-up: 6 patients (8%) were hospitalised because of an IBD flare and 18 patients (24%) needed a change in the treatment for the IBD (p < 0.001).

3.4. Predictive Factors of Poor Clinical Outcome after the Transfer

In the univariate analysis, the variables associated with a poor clinical outcome were the absence of structured transition (p = 0.007); emergency visits due to an IBD flare before transfer (p = 0.008); nutritional support before transfer (p = 0.002); body mass index (BMI) < 18.5 at transfer (p < 0.001); IBD activity at transfer (p < 0.001); faecal calprotectin > 250 µg/g at transfer (p < 0.001); C-reactive protein > 0.5 mg/dL at transfer (p < 0.001); and treatment with corticosteroids at transfer (p < 0.001) (Figure 2). Age at transfer, psychiatric comorbidity and family history of IBD were included in the univariate analysis but did not achieve statistical significance.
In the multivariable analysis, the lack of structured transition, IBD activity at transfer, BMI < 18.5 and corticosteroid treatment at transfer were predictive factors associated with a poor clinical outcome (Table 4).

3.5. Patients Lost to Follow-Up

In total, 12 patients (4%; 95% CI = 2–7) did not complete the 12 months of follow-up: 11/185 (0.06%; 95% CI = 0.03–0.11) in the transition group and 1/93 (0.01; 95% CI = 0.002–0.06) in the no-transition cohort (p > 0.05).
Regarding the patients in the transition group (11/185), one patient (1/185; 0.5%) refused to attend the IBD unit after transfer. He was an 18-year-old male patient with previous diagnosis of ileocolonic CD treated with azathioprine from the date of diagnosis. After transfer, he also decided to stop azathioprine, remaining without any IBD flare during the 12 months after transfer. The remaining 10 patients in the transition group attended the first visit in the IBD unit, but they missed the following visits according to the clinical practice of their centre. Among them, two patients were hospitalised at one year after transfer.
Finally, in the no-transition group, one patient was lost to follow-up and was hospitalised because of an IBD flare within 12 months after transfer.

4. Discussion

In the present multicentre study, the benefit of a structured transition programme from paediatric to adult IBD units has been evaluated. To our knowledge, this is the largest cohort of patients in which this outcome has been assessed. Fewer IBD flares, corticosteroid treatments, emergency visits and hospitalisations due to an IBD complication were observed among paediatric patients undergoing structured transition compared with those without transition.
Our results are consistent with other observational studies conducted in patients transferred to the adult gastroenterologist. Firstly, a British cohort reported that structured transition was associated with positive outcomes as the transition group was more likely to be corticosteroid-free one year after transfer and had less emergency visits [23]. Testa et al. also concluded that there was a significant reduction in the number of flares and hospitalisations within the 12 months after a structured transition [24]. Also, the proportion of patients in clinical remission after transfer was higher in the transition vs. in the no-transition group in an Hungarian cohort (95% vs. 65%; p = 0.037) [25], and similar data were reported in a Dutch study with a two-year follow-up after the transfer [26].
In our study, achieving remission at transfer was key for the outcomes of IBD patients, as other studies have previously reported [7,27,28]. Schutz et al. described that the proportion of patients in remission at transfer was lower in the no-transition group (63% vs. 88%); in this subgroup, IBD complications were also significantly higher at one year after transfer (64% vs. 21%) [29]. Although the proportion of patients in remission at transfer in our population was balanced between both groups (transition and no-transition), the proportion of IBD patients in remission at transfer with poor clinical outcome during the follow-up was higher in the no-transition group. This finding emphasises that a structured transition is essential in all IBD patients in our daily practice.
One of the issues regarding the benefit of transition is the definition of “successful transition”, which is still not clear because of the lack of comparative studies. Accordingly, nowadays, no specific model can be recommended yet [7,8,9]. Similarly, the number of necessary joint visits between the paediatric and the adult gastroenterologists remains unknown. Erős et al. recently published the protocol of the first randomised controlled trial aiming to provide evidence on the superiority of joint visits compared with standard transitional care in IBD [30]. In our country, the implemented model for transition between paediatric and adult gastroenterologists consists in joint visits. This model has been reported in other studies focused on transitional care [25,26,29] and follows the recommendations of the European Crohn’s and Colitis Organisation (ECCO) [7]. Based on our results, at least one joint visit could be appropriate to improve the patients’ outcomes. Moreover, the European consensus highlights that patients’ self-reported health efficacy appears to improve with age. Accordingly, in our cohort, patients in the transition group were transferred at an older age than those in the no-transition group.
Furthermore, the ECCO consensus suggests that the most commonly recommended transition models in IBD are based on a collaborative approach between paediatric and adult IBD teams, as well as a programme coordinator (in most of the cases an IBD nurse) [7]. IBD nurses are frequently the reference for patients and caregivers, and they also provide an invaluable resource for patients [6,31]. Having a dedicated outpatient clinic with nursing care is one of the quality indicators of GETECCU [32] and, in our study, of the 22 hospitals with transition, 20 (91%) had a nurse in the IBD team. On the other hand, the proportion of nutritionists involved in the transition programme in our country was low (5%). In our study, a low BMI at transfer was associated with poor clinical outcomes after transfer. Therefore, based on our results, it could be of great interest to have a multidisciplinary team, including a nutritionist, during the transition programme.
Due to the rising incidence of paediatric IBD, the number of IBD patients transferred to adult units will increase over the coming years. Our study has demonstrated that a structured transition programme improves the outcomes of IBD patients. However, resources and training for transitional care in our daily practice are scarce and, therefore, a relevant proportion of institutions do not have an established transition programme (35% of the hospitals in our study). These barriers have recently been acknowledged in a structured survey in Spain [33]. This survey was distributed to paediatric and adult gastroenterologists, and the response rate was only 12%, and it was significantly higher among paediatric vs. adult gastroenterologists. To date, there are no specific clinical guidelines for transition in IBD in Spain, unlike in other countries [5,9,10]. Therefore, based on our results, developing a clinical practice guideline about transitional care in our country could improve the management of IBD patients in this critical phase. Moreover, an appropriate transitional care should be considered as a healthcare objective that requires the support of the health system at all times. Due to the hindrances that can occur during the implementation of a transition programme, medical education about transition is key, and experienced IBD-teams should train those who have not implemented a transition programme.
The limitations of the present study are mainly those associated with its retrospective design, including the potential for missing data in clinical records. This may be a possible explanation for the low proportion of patients lost to follow-up. However, we made an effort to investigate the evolution of patients that did not attend the adult IBD unit. Also, it is worth highlighting that patients undergoing structured transition in our cohort were more likely to be clustered in larger centres with established paediatric and adult IBD units compared with the no-transition patients. Even though we also included small centres and hospitals in which the transition programme was not implemented, most of the paediatric and adult gastroenterologists involved were focused on IBD. In addition, IBD units of the no-transition groups had a referral paediatrician and, therefore, our results may not be fully extrapolated to all centres without transition.
Our collaborative study has several strengths. First, this is the largest real-world study evaluating the benefit of a transition programme in IBD patients. The retrospective design of the study allowed us to evaluate the management of transferred patients from the paediatric to the adult IBD units in a real-world setting. Moreover, flares were detected not only by hospitalisations or therapy escalation but also by objective activity index, evaluated by the Mayo score or the HBI. Finally, our study investigated the predictors of poor clinical outcome, which are key factors in our daily clinical practice.
In conclusion, our study demonstrates the benefit of a transition programme in IBD. Transition care programmes improve patients’ outcomes after the transfer from paediatric to adult IBD units. Active IBD at transfer impairs patient’s outcomes.

Author Contributions

C.R.d.C., M.J.C. and J.P.G. contributed to the study concept, designed the protocol and planned the study, analysed the data, wrote the manuscript draft and approved the submitted manuscript. C.R.d.C., J.M.-d.-C., G.P.-M., L.M.P., M.V.R.-B., R.M.-M., V.M.N.-L., M.J.C. and J.P.G. contributed to the study design, data analysis, data interpretation and writing of the manuscript and approved the submitted manuscript. All authors contributed to data collection and interpretation, identified patients for inclusion in the study, extracted data from their medical records. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by a grant from the Young Group of the Spanish Gastroenterology Association (AEG).

Institutional Review Board Statement

This study was conducted in accordance with the Declaration of Helsinki and approved by the Drug Research Ethics Committee (Comité de Ética de la Investigación con Medicamentos) at the Hospital Universitario de La Princesa in Madrid, Spain (reference number 4555).

Informed Consent Statement

Patient consent was waived in order to have an acute estimate of the benefit of the transition program: the obligation to obtain the informed consent of the patients before their inclusion in the study could have biased the inclusion towards patients who had a worse evolution and therefore had more clinic visits. Therefore, it was not mandatory to obtain the informed consent of the patients if there was no visit scheduled in the inclusion period. However, if the patient who met the inclusion criteria had a medical visit within the recruitment period, the physician informed the patient and obtained verbal acceptance of participation in the study. The exception to informed consent was approved by the Drug Research Ethics Committee.

Data Availability Statement

The data underlying this article will be shared on reasonable request to the corresponding author.

Acknowledgments

The authors wish to express thanks to Sandra Ollero for the medical writing assistance. CR is supported by a grant from the Ministerio de Economía y Competitividad (Instituto de Salud Carlos III, Rio Hortega CM21/00025) and Co-financed by the European Social Fund Plus (ESF+) “Co-financed by the European Union”.

Conflicts of Interest

Cristina Rubín de Célix has received education funding from Ferring, Tillotts Pharma, AbbVie, Norgine, MSD, Pfizer, Takeda and Janssen. Javier Martín-de-Carpi has served as a speaker, consultant and advisory member for, or has received research funding from, AbbVie Adacyte, Abbott, Casen Recordati, Cellgene, Janssen, Mead Johnson, MSD, Norgine, Nutriben, Pfizer, Faes Farma, Ferring, Kern Pharma, Nestle, Lilly, Roche, Takeda, Tillotts and Dr. Falk Pharma. Gemma Pujol-Muncunill has served as a speaker or received education founding from AbbVie, Nestlé Health Science, Janssen, Nutricia and Pfizer. Laura María Palomino has received financial support for traveling and educational activities from AbbVie, Casen Recordati, Norgine, Nestlé, Mead Johnson, Ordesa, Nutricia and Abbott. Marta Velasco Rodríguez-Belvís has received financial support for traveling and educational activities, or served as speaker or consultant for AbbVie, Casen Recordati, Norgine, Nestlé, Mead Johnson, Ordesa, Nutricia and Abbott. María José Casanova has received research or education funding from Pfizer, Takeda, Janssen, MSD, Ferring, AbbVie, Biogen, Faes Farma, Shire Pharmaceuticals, Dr. Falk Pharma, Tillotts Pharma, Chiesi and Norgine. Miriam Mañosa has served as a speaker, consultant and advisory member for, or has received research funding from, AbbVie, Galapagos, Janssen, MSD, Pfizer, Faes Farma, Takeda, Tillotts and Dr. Falk Pharma. Vicent Hernandez has served as consultant, has served as speaker, has received travel support or research funding from MSD, AbbVie, Ferring, Dr. Falk Pharma, Tillotts Pharma, Pfizer, Takeda, Janssen, Kern Pharma Biologics, Adacyte, Sandoz, Biogen and Fresenius-Kabi. Luis Menchén has served as a speaker, consultant and advisory member for, or has received research funding from, AbbVie, Galapagos, Janssen, MSD, Pfizer, Kern Pharma, Takeda, Tillotts, Ferring, Dr. Falk Pharma and General Electric. Manuel Barreiro-De Acosta has received financial support for traveling and educational activities from or has served as an advisory board member for Pfizer, MSD, Takeda, AbbVie, Kern Pharma, Janssen, Fresenius Kabi, Biogen, Ferring, Faes Farma, Shire Pharmaceuticals, Dr. Falk Pharma, Chiesi, Gebro Pharma, Otsuka Pharmaceuticals and Tillotts Pharma. Pilar Corsino has served as a speaker for, or has received research funding from, AbbVie, Janssen and Pfizer. Raquel Vicente has served as speaker, consultant and/or advisory member for, or has received research funding from, MSD, AbbVie, Pfizer, Takeda, Janssen, Ferring, Chiesi and Faes Farma. Estela Fernández-Salgado has served as speaker, consultant from AbbVie, Takeda, Janssen, Ferring and has received education funding from AbbVie, Pfizer, Takeda, Janssen, Tillotts Pharma, Dr. Falk Pharma, MSD, Faes Farma, Ferring. Sabino Riestra has served as speaker, consultant and advisory member for, or has received research funding from, MSD, AbbVie, Takeda, Janssen, Pfizer, Mylan, Biogen, Kern Pharma, Ferring, Faes Farma and Tillotts Pharma. Marta Calvo Moya has served as a speaker and consultant for, or has received research funding from, MSD, AbbVie, Takeda, Janssen, Ferring, Shire Pharmaceuticals, Tillotts Pharma, Dr. Falk Pharma and Gebro Pharma. Jose M. Huguet has served as a speaker and consultant for, or has received research funding from, MSD, AbbVie, Takeda, Janssen, Pfizer, Ferring, Sandoz, Tillotts Pharma, Dr. Falk Pharma and Faes Farma. Rocío Plaza has received education funding from AbbVie, Takeda, Janssen, Ferring, Pfizer, Tillotts Pharma and has served as a speaker for AbbVie, Takeda and Janssen. Iván Guerra has served as a speaker for Takeda and Sandoz. Teresa de Jesús Martínez-Pérez reports personal fees or nonfinancial support from Abbie, Amgen, MSD, Janssen, Takeda, Pfizer, Chiesi, Tillotts Pharma, Kern Pharma, outside the submitted work. María Calvo Iñiguez has received education funding from AbbVie, Takeda, Pfizer, Adacyte and Janssen. María Chaparro has served as a speaker, consultant and advisory member for, or received research funding from, AbbVie, Celltrion, Chiesi, Faes Farma, Dr. Falk Pharma, Ferring, Gebro Pharma, Janssen, MSD, Otsuka Pharmaceuticals, Pfizer Inc, Roche, Shire Pharmaceuticals, Takeda and Tillotts Pharma. Javier P. Gisbert has served as speaker, consultant and advisory member for, or has received research funding from, MSD, AbbVie, Pfizer, Kern Pharma, Biogen, Mylan, Takeda, Janssen, Roche, Sandoz, Celgene/Bristol Myers, Gilead/Galapagos, Lilly, Ferring, Faes Farma, Shire Pharmaceuticals, Dr. Falk Pharma, Tillotts Pharma, Chiesi, Casen Fleet, Gebro Pharma, Otsuka Pharmaceutical, Norgine and Vifor Pharma. All other authors have nothing to declare.

Abbreviations

Inflammatory bowel disease (IBD); Crohn’s disease (CD); ulcerative colitis (UC); immunomodulator (IMM); body mass index (BMI); Hazard Ratio (HR); confidence interval (CI).

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Jcm 12 04813 g001 550
Figure 1. Flow chart of the study population.
Figure 1. Flow chart of the study population.
Jcm 12 04813 g001
Jcm 12 04813 g002a 550Jcm 12 04813 g002b 550Jcm 12 04813 g002c 550Jcm 12 04813 g002d 550
Figure 2. Variables associated with poor clinical outcome. Variables associated with poor clinical outcome were analysed by Kaplan–Meier: (A) transition; (B) emergency visits due to an IBD flare before transfer; (C) nutritional support before transfer; (D) BMI < 18.5 at transfer; (E) IBD activity at transfer; (F) faecal calprotectin > 250 µg/g at transfer; (G) C-reactive protein > 0.5 mg/dL at transfer; (H) corticosteroids at transfer. Abbreviations: BMI: body mass index; IBD: inflammatory bowel disease.
Figure 2. Variables associated with poor clinical outcome. Variables associated with poor clinical outcome were analysed by Kaplan–Meier: (A) transition; (B) emergency visits due to an IBD flare before transfer; (C) nutritional support before transfer; (D) BMI < 18.5 at transfer; (E) IBD activity at transfer; (F) faecal calprotectin > 250 µg/g at transfer; (G) C-reactive protein > 0.5 mg/dL at transfer; (H) corticosteroids at transfer. Abbreviations: BMI: body mass index; IBD: inflammatory bowel disease.
Jcm 12 04813 g002aJcm 12 04813 g002bJcm 12 04813 g002cJcm 12 04813 g002d
Table
Table 1. Patient baseline demographics and disease characteristics.
Table 1. Patient baseline demographics and disease characteristics.
Transition Group
(n = 185)		No-Transition Group
(n = 93)		p Value
Gender male, n (%)115 (62)54 (58)N.S.
Age at diagnosis, years (median, IQR)12 (1–17)12 (3–17)N.S.
Age at transfer, years (median, IQR)17 (14–20)16 (14–20)<0.01
Disease duration at transfer, months (median, IQR)54 (12–211)51 (12–171)N.S.
Family history of IBD, n (%)26 (14)24 (26)<0.05
Smokers, n (%)11 (6)3 (3)N.S.
EIM, n (%)30 (16)16 (17)N.S.
Psychiatric comorbidity, n (%)37 (20.1)8 (8.7)<0.05
IBD type, n (%)CD: 106 (57)
UC: 73 (40)
IBD unclassified: 6 (3)		CD: 52 (56)
UC: 38 (41)
IBD unclassified: 3 (3)		N.S.
UC †
(n = 120)		UC extent, n (%)Ulcerative proctitis: 13 (17)
Left-sided UC: 13 (17)
Extensive UC: 11 (14)
Pancolitis: 42 (52)		Ulcerative proctitis: 3 (7)
Left-sided UC: 8 (19)
Extensive UC: 8 (19)
Pancolitis: 22 (55)		N.S.
UC severity, n (%)Never severe: 51 (65)
Ever severe: 28 (35)		Never severe: 30 (73)
Ever severe: 11 (27)		N.S.
CD
(n = 158)		CD location, n (%) ‡Distal 1/3 ileal ± limited cecal disease: 25 (24)
Colonic: 8 (8)
Ileocolonic: 66 (62)
Upper disease proximal to Treitz: 26 (25)
Upper disease distal to Treitz: 11 (10)		Distal 1/3 ileal ± limited cecal disease: 7 (14)
Colonic: 9 (17)
Ileocolonic: 36 (69)
Upper disease proximal to Treitz: 11 (21)
Upper disease distal to Treitz: 1 (2)		N.S.
CD behaviour, n (%)Inflammatory: 86 (81)
Stricturing: 16 (15)
Penetrating: 3 (3)
Penetrating and stricturing: 1 (1)		Inflammatory: 47 (90)
Stricturing: 2 (4)
Penetrating: 3 (6)
Penetrating and stricturing: 0 (0)		N.S.
Growth delay, n (%)20 (19)6 (12)N.S.
Perianal disease, n (%)32 (30)10 (19)N.S.
IBD: inflammatory bowel disease; CD: Crohn’s disease; UC: ulcerative colitis; EIM: extraintestinal manifestations; IQR: interquartile range; N.S.: nonstatistically significant. † We included both UC and IBD unclassified. ‡ Patients may belong to more than one group.
Table
Table 2. Characteristics of the participating hospitals.
Table 2. Characteristics of the participating hospitals.
Transition Group
(n = 22)		No-Transition Group
(n = 12)		p Value
Third-level hospital
(paediatric unit), n (%)		17 (77)6 (50)N.S.
Third-level hospital
(gastroenterology unit), n (%)		16 (73)6 (50)N.S.
Paediatric IBD unit (yes), n (%)15 (68)1 (8)<0.01
Gastroenterology IBD unit (yes), n (%)22 (100)8 (67)<0.01
IBD patients followed-up in
paediatric units (median, IQR)		28 (43)15 (70)N.S.
IBD patients followed-up in gastroenterology units (median, IQR)1700 (1126)1075 (1250)N.S.
Transition programme starting date, n (%)<2010: 1 (4)
2010–2015: 8 (37)
2016–2020: 12 (55)
>2020: 1 (4)		NANA
Transfer type (no-transition), n (%)NAIBD specialist: 11 (92)
General gastroenterologist: 1 (8)		NA
Number of patients transferred per year (median, IQR)3 (3)NA
Transition place, n (%)Paediatric clinic: 3 (14)
Gastroenterology clinic: 10 (45)
Both clinic: 9 (41)		NANA
Number of joint visits (mean ± SD)1.5 ± 0.8NANA
Transition duration (median, IQR), months6 (6)NANA
Professionals involved in transition, n (%)Paediatrician and
gastroenterologist: 21 (100)
Paediatric nurse: 7 (33)
Gastroenterology nurse 13 (62)
Nutritionist: 1 (5)
Social worker: 0 (0)		NANA
Paediatrician focused on IBD, n (%)19 (91)NANA
Gastroenterologist focused on IBD, n (%)21 (100)NANA
IBD: inflammatory bowel disease; SD: standard deviation; IQR: interquartile range; NA: not applicable; N.S.: nonstatistically significant.
Table
Table 3. Clinical outcomes.
Table 3. Clinical outcomes.
OUTCOMES BEFORE TRANSFER
Transition Group
(n = 185)		No-Transition Group
(n = 93)		p Value
Emergency visits, n (%)57 (31)44 (47)<0.01
Hospitalisations, n (%)77 (42)44 (47)N.S.
Surgeries, n (%)23 (12)7 (8)N.S.
IBD-related treatments, n (%)Aminosalicylates: 94 (51)
Topic treatment: 50 (27)
Corticosteroids: 91 (49)
IMM: 145 (78)
Biologic drugs: 100 (54)
EEN: 58 (31)
Apheresis: 5 (3)
Nutritional support: 21 (11)		Aminosalicylates: 59 (63)
Topic treatment: 28 (30)
Corticosteroids: 55 (59)
IMM: 76 (82)
Biologic drugs: 38 (41)
EEN:31 (33)
Apheresis: 2 (2)
Nutritional support: 17 (18)		<0.05
N.S.
N.S.
N.S.
<0.05
N.S.
N.S.
N.S.
OUTCOMES ONE YEAR AFTER TRANSFER
IBD flare, n (%)41 (22)33 (36)<0.05
Emergency visits, n (%)18 (10)16 (17)N.S.
Hospitalisations, n (%)6 (3)9 (10)<0.05
Surgeries, n (%)2 (1)3 (3)N.S.
IBD-related treatments, n (%)Aminosalicylates: 74 (40)
Topic treatment: 20 (11)
Corticosteroids: 9 (5)
IMM: 95 (51)
Biologic drugs: 98 (53)
Nutritional support: 2 (1)		Aminosalicylates: 44 (47)
Topic treatment: 7 (8)
Corticosteroids: 15 (16)
IMM: 58 (62)
Biologic drugs: 44 (47)
Nutritional support: 1 (1)		N.S.
N.S.
<0.01
N.S.
N.S.
N.S.
IBD: inflammatory bowel disease; IMM: immunomodulators; EEN: exclusive enteral nutrition; N.S.: nonstatistically significant.
Table
Table 4. Multivariable analysis of factors associated with poor clinical outcome.
Table 4. Multivariable analysis of factors associated with poor clinical outcome.
FactorHR95% CI
No transition2.11.3–3.3
IBD activity at transfer4.93.1–7.9
BMI < 18.5 at transfer1.91.1–3.3
Corticosteroids at transfer4.92.2–10.9
IBD: inflammatory bowel disease; BMI: body mass index; HR: hazard ratio; CI: confidence interval.
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MDPI and ACS Style

Rubín de Célix, C.; Martín-de-Carpi, J.; Pujol-Muncunill, G.; Palomino, L.M.; Velasco Rodríguez-Belvís, M.; Martín-Masot, R.; Navas-López, V.M.; Ricart, E.; Casanova, M.J.; Rodríguez-Martínez, A.; et al. Benefits of Paediatric to Adult Transition Programme in Inflammatory Bowel Disease: The BUTTERFLY Study of GETECCU and SEGHNP. J. Clin. Med. 2023, 12, 4813. https://doi.org/10.3390/jcm12144813

AMA Style

Rubín de Célix C, Martín-de-Carpi J, Pujol-Muncunill G, Palomino LM, Velasco Rodríguez-Belvís M, Martín-Masot R, Navas-López VM, Ricart E, Casanova MJ, Rodríguez-Martínez A, et al. Benefits of Paediatric to Adult Transition Programme in Inflammatory Bowel Disease: The BUTTERFLY Study of GETECCU and SEGHNP. Journal of Clinical Medicine. 2023; 12(14):4813. https://doi.org/10.3390/jcm12144813

Chicago/Turabian Style

Rubín de Célix, Cristina, Javier Martín-de-Carpi, Gemma Pujol-Muncunill, Laura María Palomino, Marta Velasco Rodríguez-Belvís, Rafael Martín-Masot, Víctor Manuel Navas-López, Elena Ricart, María José Casanova, Alejandro Rodríguez-Martínez, and et al. 2023. "Benefits of Paediatric to Adult Transition Programme in Inflammatory Bowel Disease: The BUTTERFLY Study of GETECCU and SEGHNP" Journal of Clinical Medicine 12, no. 14: 4813. https://doi.org/10.3390/jcm12144813

APA Style

Rubín de Célix, C., Martín-de-Carpi, J., Pujol-Muncunill, G., Palomino, L. M., Velasco Rodríguez-Belvís, M., Martín-Masot, R., Navas-López, V. M., Ricart, E., Casanova, M. J., Rodríguez-Martínez, A., Leo-Carnerero, E., Alcaraz, A., Mañosa, M., Hernández, V., Cobelas Cobelas, M. C., Sánchez, C., Menchén, L., Mesonero, F., Barreiro-De Acosta, M., ... Gisbert, J. P. (2023). Benefits of Paediatric to Adult Transition Programme in Inflammatory Bowel Disease: The BUTTERFLY Study of GETECCU and SEGHNP. Journal of Clinical Medicine, 12(14), 4813. https://doi.org/10.3390/jcm12144813

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