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e170

Abstracts of the 22

nd

National Congress of Digestive Diseases / Digestive and Liver Disease 48S2 (2016) e67–e231

Results:

Male were more represented in groups C (60%), D (75%), E

(75%) (p=0.03), whereas mean age was similar in all groups (p=0.57).

Erosive esophagitis was more represented in groups C (70%), D

(50%), E (50%) (p=0.018). Acid exposure time increased progressively

from group A to E (A 4.3[IQR 5.6]; B 8.2[8.4]; C 9[5.7]; D 9.1[11.3];

E 10.2[7.4]; p=0.014). Total number of reflux events was higher in

C and D groups (A 45.3[IQR 20.7]; B 49[85]; C 96[71]; D 80[37.5];

E 57.5[76.7]; p=0.008). Mean DCI during WS, DCI-MRS and MRS/

WS ratio were progressively lower from A to E group (p<0.001 with

ANOVA). The Bonferroni test showed significant differences between

A, B, C, versus D and E (p<0.001). Details are reported in table 1.

Conclusions:

Data on GERD evidence at impedance-pH monitoring

demonstrated that IEM should be considered as clinically relevant

when the frequency of failed or weak WS is ≥60%.

P.08.14

A PROSPECTIVE APPLICATION OF THE ESPGHAN GUIDELINES IN A

SYMPTOMATIC ADULT POPULATION

Efthymakis K.*, Serio M., D’Amato D., Milano A., Laterza F.,

Bonitatibus A., Neri M.

Department of Medicine and Ageing Sciences, “G.D’Annunzio”

University and Foundation, Chieti, Italy

Background and aim:

Current adult guidelines require histological

confirmation of celiac disease (CD). However, recent pediatric

guidelines have proposed algorithms to reduce the need for biopsy

in genetically susceptible symptomatic children. We explore

the applicability of the current ESPGHAN criteria and assess the

accuracy of serology in detecting villous atrophy in a prospective

cohort of symptomatic adults.

Material and methods:

We recruited 234 consecutive symptomatic

adults (mean age=33.9ys) showing EMA positivity and genetic

susceptibility. All patients underwent upper endoscopy with

multiple biopsy sampling in the duodenum. Histological lesions

were graded according to the Corazza-Villanacci classification and

considered diagnostic for grades>B. Anti-tTG titers were assessed

with 12 different assays; one ELISA kit (specified Upper Limit of

Normal=3.5U/ml) was used in 141 subjects (60.3%), while a second

one in 59 (25.2%, ULN=9.9U/ml). Accuracy of anti-tTG testing and

optimal cut-off levels were determined by means of a ROC curve.

Performance was also calculated for a cut-off 10 times ULN.

Results:

Mean anti-tTG levels at inclusion were 71.1±4.4U/ml, while

mean adjusted levels (anti-tTG/ULN) were 14.8±0.9 times ULN

(mean±SE). Among the 234 patients,21 (9%) showed no atrophy;

partial and total atrophy were present in 85 (36.3%) and 128 (54.7%)

respectively. Anti-tTG levels significantly correlated to the degree

of villous atrophy (p<0.001; rs=0.397, p<0.001). AUC proved a fair

diagnostic accuracy both for unadjusted and adjusted anti-tTG

levels (respectively 0.803, 0.807; p<0.01). For the ESPGHAN criterion

of anti-tTG=10 times ULN, a positive predictive value (PPV) of 97.7%

was calculated (sensitivity=59.2%, specificity=86.9%). The optimal

cut-off for adjusted anti-tTG levels was 16 times ULN, with a PPV

of 98.9% (sensitivity=41.2%, specificity=95.7%). Considering different

assays, results were puzzling; although in the first one PPV (=97.14%)

seemed to peak at 50U/ml (14.3 times ULN), the second assay proved

considerably more predictive: for a cut-off=37.3U/ml (3.7 times

ULN) it showed a superior PPV=100% (sensitivity 53.1%, specificity

100%). This persisted after standardization (cut-offs -0.14 vs -1.2).

Conclusions:

In adult symptomatic patients with EMA positivity and

genetic susceptibility, anti-tTG titers predict severity of duodenal

atrophy. Multiples of ELISA cut-off values can be applied to diagnose

CD in a subset of adult patients. Measured values are assay-specific,

intrinsically difficult to compare and not scale-dependent in our

study. Thus, ESPGHAN criteria can be applied in adults but are

sub-optimal for the purpose of achieving uniform prediction of

atrophy. Our findings could prove useful when assessing equivocal

histological cases, and could help in guiding patient follow-up.

P.08.15

INCREASED INTRA-BOLUS PRESSURE IS ASSOCIATED WITH NON-

CARDIAC CHEST PAIN AND NEGATIVE ENDOSCOPY – A STUDY

USING HIGH-RESOLUTION MANOMETRY

Della Coletta M.*

2

, Galeazzi F.

2

, Marabotto E.

3

, De Bortoli N.

4

,

Marchi S.

4

, Tolone S.

5

, Savarino V.

3

, Savarino E.

1

1

Reparto di Gastroenterologia, Dipartimento di Chirurgia, Oncologia

e Gastroenterologia, Università di Padova, Padova, Italy,

2

Divisione

di Gastroenterologia, Dipartimento di Chirurgia, Oncologia e

Gastroenterologia, Università di Padova, Padova, Italy,

3

Divisione di

Gastroenterologia, Dipartimento di Medicina Interna, Università di

Genova, Genova, Italy,

4

Divisione di Gastroenterologia, Dipartimento di

Medicina Interna, Università di Pisa, Pisa, Italy,

5

Divisione di Chirurgia

Generale e Bariatrica, Dipartimento di Chirurgia, Seconda Università

di Napoli, Napoli, Italy

Background and aim:

High Resolution Manometry (HRM) is

currently considered the gold standard to assess esophageal

peristalsis and esophago-gastric junction (EGJ) function. Indeed,

with the use of this technology novel validated metrics have been

developed to define esophageal motility abnormalities. In particular,

the intrabolus pressure (IBP) has been initially regarded as an

indirect measure of bolus transit trough the EGJ, although the last

iteration of Chicago Classification lacks of its adoption because of

the paucity of data in this regard. We aimed to investigate whether

patients with non-cardiac chestpain (NCCP) and reflux-related

heartburn (RH) may present different IBP values and which is its

pathophysiological role.

Material andmethods:

We included consecutive patients with NCCP

or RH as stand-alone symptom, referring to our motility laboratory.

Patientswithgastro-intestinal surgery, achalasiaor sclerodermawere

excluded. All patients underwent esophagogastroduodenoscopy

(EGDS) and HRM with 5-min baseline recording and 10 single

water swallows. The diagnostic criteria agreed with the Chicago

Classification vers. 2. Data were expressed as mean and standard

deviation. A t-test and x2 analysis were performed to compare data.

A p-value < 0.05 was considered statistically significant.

Results:

Between March 2014 and March 2015, we included 24

patients (9 Male, 56±15 years) with NCCP and 47 patients (50±13

years; 19 M) with RH. No differences in terms of age, sex, BMI,

manometry patterns and esophagogastric junction morphologies

were found between the two groups (p=ns). Patients with NCCP

had a mean IBP higher than patients with RH (18.6±6.7 vs. 14.1±4.7;

p=0.02). Mean DCI (79±36 vs. 82±35; p=0.7) and resting pressure

(30±12vs. 22±11; p=0.06) were similar between the two groups

groups. Only 1/24 patients (4%) of the NCCP patients had endoscopic

evidence of GERD, while in RH group the number was higher (13/47;

28%; p=0.02).

Conclusions:

The IBP is the only HRM metric that differed between

patients with NCCP and those with RH supporting its diagnostic

usefulness in distinguishing them and suggesting that NCCP

elicitation can be more related to reduced distal oesophageal

compliance as a whole (i.e. abnormal bolus transit and EGJ

dysfunction) rather than abnormal vigor of peristalsis. Finally,

an increased IBP well correlated with a negative endoscopy, thus

reflecting a potential role of IBP in contrasting reflux occurrence.