OBJECTIVES: Patients who have undergone pancreaticoduodenectomy (PD) may experience a long-term decrease in quality of life because of postoperative pancreatic dysfunction (such as digestive and absorption disorders) and fatty liver as a result of combined resection of the duodenum, gallbladder, and bile duct. The present study investigated the usefulness of pancrelipase for the prevention of pancreatic dysfunction after PD. METHODS: The data from 73 patients who underwent PD in a single institution were analyzed. Patients who underwent PD during 2007-2011 were administered the low-titer pancreatic enzyme preparations berizym® and pancreatin® (first period group), while patients who underwent PD during 2012-2017 were administered the high-titer pancreatic enzyme preparation pancrelipase (second period group). The following measures of the nutrition status were examined before and after PD: serum albumin concentration, total lymphocyte count, serum total cholesterol concentration, body mass index, controlling nutrition status (CONUT) index, Onodera's prognostic nutrition index (PNI), and liver computed tomography values. RESULTS: The second period group had significantly higher serum albumin concentrations at 3 and 6 months postoperatively, serum total cholesterol concentrations at 1 month postoperatively, and Onodera's PNI values at 3 and 6 months postoperatively than the first period group. The CONUT index values at 6 months after PD were significantly lower in the second period group than in the first period group. CONCLUSIONS: Pancrelipase is useful in improving the nutrition status and preventing fatty liver after PD.
OBJECTIVES: Patients who have undergone pancreaticoduodenectomy (PD) may experience a long-term decrease in quality of life because of postoperative pancreatic dysfunction (such as digestive and absorption disorders) and fatty liver as a result of combined resection of the duodenum, gallbladder, and bile duct. The present study investigated the usefulness of pancrelipase for the prevention of pancreatic dysfunction after PD. METHODS: The data from 73 patients who underwent PD in a single institution were analyzed. Patients who underwent PD during 2007-2011 were administered the low-titer pancreatic enzyme preparations berizym® and pancreatin® (first period group), while patients who underwent PD during 2012-2017 were administered the high-titer pancreatic enzyme preparation pancrelipase (second period group). The following measures of the nutrition status were examined before and after PD: serum albumin concentration, total lymphocyte count, serum total cholesterol concentration, body mass index, controlling nutrition status (CONUT) index, Onodera's prognostic nutrition index (PNI), and liver computed tomography values. RESULTS: The second period group had significantly higher serum albumin concentrations at 3 and 6 months postoperatively, serum total cholesterol concentrations at 1 month postoperatively, and Onodera's PNI values at 3 and 6 months postoperatively than the first period group. The CONUT index values at 6 months after PD were significantly lower in the second period group than in the first period group. CONCLUSIONS: Pancrelipase is useful in improving the nutrition status and preventing fatty liver after PD.
Pancreaticoduodenectomy (PD) is the standard operative procedure most commonly used
to remove lesions located in the pancreatic head. In some cases, PD results in deteriorated
quality of life because of postoperative pancreatic dysfunction (such as digestive and
absorption disorders) and fatty liver due to combined resection of the duodenum, gallbladder,
and bile duct.[1,2] Studies have reported that pancreatic dysfunction typified by chronic
pancreatitis is effectively managed via the administration of a newly available high-titer
pancreatic enzyme preparation called pancrelipase.[3,4] Therefore, we investigated the
usefulness of pancrelipase in preventing pancreatic dysfunction after PD.
Materials and Methods
The present study included 73 patients who underwent PD at the Department of
Gastroenterological Surgery of Fujita Health University between 2007 and 2017. Patients who
underwent PD between 2007 and 2011 were administered the low-titer pancreatic enzyme
preparations berizym® and pancreatin® (first period group), while patients
who underwent PD between 2012 and 2017 were administered the high-titer pancreatic enzyme
preparation pancrelipase (second period group). The two groups were compared regarding
background characteristics, age, sex, body mass index, condition for which PD was performed,
extent of lymph node dissection, presence or absence of total nerve dissection, reconstruction
method, preoperative examination data (serum albumin concentration, total lymphocyte count,
serum total cholesterol concentration, Onodera’s prognostic nutrition index (PNI),[5] controlling nutrition status (CONUT) index,[6] and liver computed tomography (CT) values), and
duration of postoperative hospitalization. Additionally, the nutrition status was measured via
assessments of the serum albumin concentrations, total lymphocyte counts, serum total
cholesterol concentrations, Onodera’s PNI values, CONUT index values, and liver CT values before
PD and at 1, 3, 6, and 12 months after PD.The present study was approved by the Medical Research Ethics Committee of Fujita
Health University (approval no. HM17-372). Informed consent was not required due to the
retrospective nature of the study.
Statistical Analysis
Data were analyzed using IBM SPSS statistics 22.0 (IBM Japan, Inc., Tokyo, Japan)
Student’s t-tests and chi-squared tests were used to assess the significance of intergroup
differences. P<0.05 was considered statistically significant.
Results
Between 2007 and 2017, 128 patients underwent pancreatectomy, while 73 patients
underwent PD in our department. Of the patients who underwent PD, 34 were in the first period
group, while 39 were in the second period group. The only preoperative background
characteristics that significantly differed between the first period group and the second period
group were the condition for which PD was performed and the liver CT value (Table 1). In all patients, the reconstruction method was
subtotal stomach-preserving pancreaticoduodenectomy-II, in which the anastomoses of the jejunum
are performed in the order of pancreas, bile duct, and stomach from the oral side.
Table1
Preoperative patient background characteristics
First period groups
Second period groups
p-values
Age
65.9
70.0
0.144
Gender (M:F)
23:11
23:16
0.451
BMI (kg/m2)
28.4
21.1
0.256
Disease
PDAC
14
17
0.018*
BD Ca
11
3
Pap. Ca
5
3
IPMC
1
6
IPMA
3
6
Other
0
4
Lymph node dissection (D1:D2)
4:30
14:25
0.451
Plexus dissection (+:–)
14:20
17:22
0.838
Serum albumin levels
4.0
4.1
0.509
Total lymphocyte counts
1392.8
1591.5
0.148
Serum total cholesterol levels
188.4
194.5
0.450
Onodera’s PNI
47.2
49.0
0.143
CONUT score
1.9
1.2
0.051
Liver CT values
54.6
59.2
0.003*
Hospital Stay
54.9
68.4
0.602
*: significantly different
BMI: body mass index, PDAC: pancreatic ductal adenocarcinoma, BD Ca: distal
carcinoma of bile duct , Pap. Ca: carcinoma of papilla of Vater, IPMC: Intra-ductal Papillary
mucinous carcinoma, IPMA: Intra-ductal Papillary mucinous adenoma
The serum albumin concentrations at 3 and 6 months after PD were significantly
higher in the second period group than in the first period group (Figure 1). There was no significant difference in the total lymphocyte count between
the groups (Figure 2). The serum total cholesterol
concentration at 1 month after PD was significantly higher in the second period group than in
the first period group (Figure 3). The Onodera’s PNI values
at 3 and 6 months after PD were significantly higher in the second period group than in the
first period group (Figure 4). The CONUT index value at 6
months after PD was significantly lower in the second period group than in the first period
group (Figure 5). The liver CT values before and at 1 month
after PD were significantly lower in the first period group than in the second period group
(Figure 6).
Figure 1
Changes in serum albumin concentrations in patients who underwent pancreaticoduodenectomy in
the first period (with low-titer digestive enzyme preparations) versus the second period (with
high-titer pancrelipase)
The serum albumin concentrations at 3 and 6 months postoperatively were
significantly higher in the second period group (white bar) than in the first period group
(black bar).
*p<0.05
Figure 2
Changes in total lymphocytes counts in patients who underwent pancreaticoduodenectomy in the
first period (with low-titer digestive enzyme preparations) versus the second period (with
high-titer pancrelipase)
There was no significant intergroup difference in the total lymphocyte count.
Figure 3
Changes in serum cholesterol in patients who underwent pancreaticoduodenectomy in the first
period (with low-titer digestive enzyme preparations) versus the second period (with
high-titer pancrelipase)
The serum total cholesterol concentrations at 1 month postoperatively were
significantly higher in the second period group (white bar) than in the first period group
(black bar).
*p<0.05
Figure 4
Changes in the Onodera’s prognostic nutrition index (PNI) values of the patients who
underwent pancreaticoduodenectomy in the first period (with low-titer digestive enzyme
preparations) versus the second period (with high-titer pancrelipase)
The Onodera’s PNI values at 3 and 6 months postoperatively were significantly
higher in the second period group (white bar) than in the first period group (black bar).
*p<0.05
Figure 5
Changes in the controlling nutrition status (CONUT) index values of the patients who
underwent pancreaticoduodenectomy in the first period (with low-titer digestive enzyme
preparations) versus the second period (with high-titer pancrelipase)
CONUT index values at 6 months postoperatively were significantly lower in the
second period group (white bar) than in the first period group (black bar).
*p<0.05
Figure 6
Changes in the liver computed tomography values of the patients who underwent
pancreaticoduodenectomy in the first period (with low-titer digestive enzyme preparations)
versus the second period (with high-titer pancrelipase)
The liver computed tomography values before surgery and at 1 month postoperatively
were significantly lower in the first period group (black bar) than in the second period group
(white bar).
*p<0.05
Discussion
The safety of PD has been increased by improvements in preoperative diagnosis,
surgical procedure, and postoperative management, resulting in fewer perioperative complications
such as pancreatic fistula.[7] Additionally, the
postoperative outcome of PD for pancreatic carcinoma has been improved by advances in adjuvant
chemotherapy, with some patients achieving long-term survival.[8] However, long-term survivors after PD can experience long-term
complications because of pancreatic dysfunction.The digestion and absorption of fat are closely related to pancreatic function.
Pancreatic juice contains lipase, which hydrolyzes orally ingested fat to produce free fatty
acids that are subsequently micellized by bile acid. The micellized fatty acids are absorbed via
the epithelial cells of the small intestine, then mostly migrate to the portal vein system, and
are metabolized in the liver to rapidly produce a source of energy. A minority of these
micellized fatty acids migrate to the thoracic duct via lymph channels. After PD, the
concentrations of various digestive enzymes in the pancreatic juice are relatively reduced, and
the pancreatic juice secretion decreases because of the reduced secretion of cholecystokinin and
secretin resulting from resection of the duodenum. Steatorrhea reportedly occurs when the
amylase secretion level is ≤15% of that in healthy subjects,[9] or when the lipase secretion level decreases to ≤10% of that in healthy
subjects.[10]It is important to consider the possibility of digestive and absorption disorders
when managing patients after PD. In most cases of pancreatic ductal adenocarcinoma, pancreatic
fibrosis is highly advanced preoperatively because of the concomitant pancreatitis that develops
because of the occlusion of the main pancreatic duct. Additionally, malnutrition is worsened
because of nervous diarrhea, as the nerve plexuses around the superior mesenteric artery are
often completely removed to achieve a radical cure. This disrupts the digestion and absorption
of fat, resulting in malnutrition. Furthermore, there is an increase in the conversion of
carbohydrates to fat in the liver, causing the development of fatty liver.Treatment options for digestive and absorption disorders include digestive enzyme
replacement therapy. The development of digestive enzyme preparations started with the
formulation of the world’s first therapeutic preparation (taka-diastase) in 1899.[11] Diastase and biodiastase were developed
approximately 50 years later, while pancreatin derived from porcine pancreas was developed in
1953 and remained in mainstream use until recently. However, compared with conventional
pancreatin, the enzymatic activities of lipase, amylase, and protease are eight, six, and seven
times higher, respectively. Thus, highly extracted/purified pancreatin from porcine pancreas was
used to create pancrelipase, which is a high-titer preparation with an enteric coating to
prevent inactivation in the stomach.[12]
LipaCreon® is a high-titer pancrelipase formulation that has been covered by the
national insurance system in Japan since 2011 for pancreatic secretion insufficiency represented
by chronic pancreatitis.[3,4] Kuroda et al.[13]
reported that 20,000–50,000 units of fat digestion activity per meal are required to be
supplemented in a patient with pancreatic dysfunction. As the fat digestibility per gram of
pancrelipase is apparently greater than other enzyme preparations, pancrelipase is the current
mainstream therapeutic medication for patients with pancreatic dysfunction.[9,13]In the present study, the nutritional status after PD showed a tendency to recover
almost to the preoperative value from 6 months to 1 year postoperatively. However, the
improvement in the nutritional status took longer in the first period group (patients who
received conventional low-titer digestive enzyme preparations) than in the second period group
(patients who received the high-titer digestive enzyme preparation pancrelipase).There were significant differences in the background diseases in the first period
group versus the second period group. However, the main reason that the characteristics of the
background diseases in each group is important is because pancreatic ductal adenocarcinoma
accompanied by concomitant pancreatitis, lymph node dissection, and nerve plexus dissection
causes postoperative malabsorption. Thus, as the incidences of pancreatic ductal adenocarcinoma
in both groups were similar, the impact of the intergroup difference in the background diseases
was likely to be minimal.As the preoperative liver CT values were also significantly different between the
two groups, this parameter could not be used to evaluate postoperative intergroup differences in
nutritional status. However, there were no preoperative intergroup differences in the serum
concentrations of albumin and total cholesterol, and the Onodera’s PNI and CONUT index values.
The postoperative evaluations of these indicators showed that the nutritional status was
significantly better in the second period group (who received the high-titer digestive enzyme
preparation pancrelipase) than in the first period group (who received low-titer digestive
enzyme preparations).
Conclusion
High-titer pancrelipase as part of nutrition management is useful for improving the
nutritional status and preventing fatty liver after PD.
Authors: J Ignacio de Ulíbarri; A González-Madroño; N G P de Villar; P González; B González; A Mancha; F Rodríguez; G Fernández Journal: Nutr Hosp Date: 2005 Jan-Feb Impact factor: 1.057
Authors: Thilo Hackert; Milena Sachsenmaier; Ulf Hinz; Lutz Schneider; Christoph W Michalski; Christoph Springfeld; Oliver Strobel; Dirk Jäger; Alexis Ulrich; Markus W Büchler Journal: Ann Surg Date: 2016-09 Impact factor: 12.969
Authors: T Nakamura; K Takebe; K Kudoh; M Ishii; K Iamura; H Kikuchi; F Kasai; Y Tandoh; N Yamada; Y Arai Journal: J Gastroenterol Date: 1995-02 Impact factor: 7.527
Authors: David C Whitcomb; Amit Bodhani; Katrin Beckmann; Suntje Sander-Struckmeier; Shufang Liu; Mahesh Fuldeore; Paul F Pollack; Rupal P Khurmi Journal: Pancreas Date: 2016 May-Jun Impact factor: 3.327