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- •Contents
- •About the Editors
- •1.1 Introduction
- •References
- •1.3 Surgical Procedure
- •1.5 Early Postoperative Care
- •1.6 Surgical Complications
- •1.7 Islet Function
- •1.9 Pain Resolution
- •1.10 Conclusions
- •2.1 Background
- •2.3 Video Cholangioscope: Mother–Baby Systems
- •2.5 Direct per-Oral Cholangioscopy
- •2.6 Indications
- •2.7.1 Intraductal Lithotripsy
- •2.7.2 Bile Duct Stones
- •2.7.3 Indeterminate Biliary Strictures
- •2.7.4 Primary Sclerosing Cholangitis (PSC)
- •2.7.5 Pancreatic Neoplasms
- •2.8 Other Applications
- •2.9 Complications
- •2.11 Conclusion
- •References
- •3.1 Introduction
- •3.3 Epidemiology
- •3.4 Aetiopathogenesis
- •3.5 Pathology
- •3.5.1 Ultrastructure
- •3.6 Haemodynamics
- •3.7 Clinical Features
- •3.8 Laboratory Features
- •3.9 Imaging
- •3.10 Endoscopy
- •3.11 Hepatic Venous Pressure Gradient
- •3.12 Liver Biopsy
- •3.14 Differential Diagnosis
- •3.15 Management
- •3.15.1 Acute Variceal Bleeding
- •3.17 Summary
- •References
- •4.1 Anal Fistula
- •4.1.1 Etiology
- •4.1.2 Evaluation: Pathology
- •4.1.3 Evaluation: Radiology
- •4.1.5 Management
- •4.1.5.1 Medical
- •4.1.5.2 Surgical
- •4.1.8 Special Scenarios: Anal Fistulas
- •4.2 Hemorrhoids
- •4.2.1 Internal Hemorrhoids
- •4.2.2 External Hemorrhoids
- •4.2.3 Etiology
- •4.2.4 Medical Treatment
- •4.2.4.1 TONE Concept
- •4.2.5.1 Rubber Band Ligation
- •4.2.5.2 Sclerotherapy
- •4.2.5.3 Infrared Coagulation
- •4.2.6 Surgical Management
- •4.2.6.1 Thrombosed External Hemorrhoids
- •4.2.6.2 Acute Hemorrhoid Crisis
- •4.2.6.3 Hemorrhoidectomy
- •4.2.6.4 Stapled Hemorrhoidopexy
- •4.2.6.5 Doppler-Guided Hemorrhoidal Artery Ligation
- •4.3 Anal Fissure
- •4.3.1 Pathophysiology
- •4.3.2 Diagnosis
- •4.3.4 Medical Treatment
- •4.3.6 Botulinum Toxin (Botox) Injection
- •4.3.7 Surgical Management
- •4.3.7.1 Lateral Internal Sphincterotomy (LIS)
- •4.3.7.2 Local Advancement Flaps
- •4.4 Pilonidal Sinus Disease
- •4.4.1 Introduction
- •4.4.2 Asymptomatic Pit Treatment
- •4.4.3 Acute Abscess Treatment
- •4.4.4 Chronic Disease Treatments
- •4.4.4.3 Pit-Picking Techniques
- •4.4.6 Minimally Invasive Surgical Techniques
- •4.4.8 Conclusions
- •References
- •5.1 Introduction
- •5.3.1 Genotype-Phenotype Correlation
- •5.3.3 Histology
- •5.3.4 Benign Recurrent Intrahepatic Cholestasis (BRIC)
- •5.4.1 Genotype-Phenotype Correlation
- •5.4.4 Histology
- •5.5.1 Genotype-Phenotype Correlation
- •5.5.3 Histology
- •5.5.5 Low Phospholipid-Associated Cholelithiasis (LCAP)
- •5.7 TJP2 Mutations
- •5.8 NR1H4 (FXR) Mutations
- •5.9 Myosin-5B (MYO5B) Mutations
- •5.11.1 Low GGT Versus High GGT Cholestasis
- •5.14 New Treatment Targets
- •5.15 Conclusion
- •References
- •5.12 Management
- •5.12.1.2 Other Treatments
- •5.12.1.3 Surgical Diversion
- •5.12.2 Nutritional Rehabilitation
- •5.12.3 Liver Transplantation
- •5.13 Surveillance
- •6.1 Introduction
- •6.3.1 Fellowship Programs
- •6.3.3 Our Experience
- •6.3.4 Collaboration Between Centers
- •6.4 Who Should Credential Multi-Organ Retrieval?
- •6.5 Conclusion
- •References
- •7.1 Introduction
- •References
- •8.1 Introduction
- •8.2.3 Functional Imaging
- •8.4.1 Molecular-Based Biomarkers
- •8.4.2 Circulating Tumour Cells
- •8.4.3 Circulating Tumour DNA (ctDNA)
- •8.5 Conclusion
- •References
- •9.1 Introduction
- •9.2 Background
- •9.6 Role of PBT in Pancreatic Cancer
- •9.9 Role of PBT in Anal Canal Carcinoma
- •9.10 Conclusions
- •References
- •10.1 Introduction
- •10.2.2 Tolerance
- •10.2.3 Early Clinical Immunosuppression
- •10.6 Allorecognition
- •10.9 Tolerogenesis
- •10.10.1 Chronic Rejection
- •10.11 A Survey
- •10.12 Induction Therapy (Routine Cases)
- •10.13 Maintenance Therapy (Routine Cases)
- •10.16 Infection Prophylaxis
- •10.17 Rejection Management
- •10.20 Steroid-Resistant Rejection (ACR)
- •10.21 Antibody-Mediated Rejection (AMR)
- •10.22 Chronic Rejection
- •10.23 Graft vs. Host Disease
- •10.26 PTLD Encountered
- •10.27 Other Cancers Encountered
- •10.29 ABO Incompatible Liver Transplant
- •10.30 Comments From Experience
- •Appendix
- •Standard Induction
- •Standard Maintenance
- •Rejection Management
- •ABOi Liver Transplant
- •References
- •11.4.1 IPMN
- •11.4.2 Mucinous Cystic Tumours
- •11.4.4 Solid Pseudopapillary Epithelial Neoplasm (SPEN)
- •11.4.5 Cystic PNET
- •11.5.1 Targeting Mitogenic Signalling
- •11.5.2 Targeting Angiogenesis
- •11.5.3 Targeting Immune Checkpoints
- •11.7.4 Initial Management
- •11.7.8 Postoperative Complications
- •11.8.1 Surgical Risk Assessment
- •11.8.2 Child-Turcotte-Pugh (CTP) Score
- •11.8.5 Mayo Risk Score
- •11.8.6 MELD Na Score
- •11.10.1 Step 1
- •11.10.2 Step 2
- •11.10.3 Step 3
- •11.10.4 Step 4
- •11.10.5 Step 5
- •References

13
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1 Total Pancreatectomy andIslet Autotransplantation forChronic Painful Pancreatitis

17© The Author(s), under exclusive license to Springer Nature Singapore Pte
Ltd. 2022
P. Sahni, S. Pal (eds.), GI Surgery Annual, GI Surgery Annual 26,
https://doi.org/10.1007/978-981-19-0828-6_2
Chapter 2
Cholangiopancreaticoscopy: ADistinct
Diagnostic andTherapeutic Tool
intheCurrent Era
SumitBhatia, SukritSud, andRandhirSud
2.1 Background
Direct visualization of the bile duct and pancreatic duct using per-oral endoscopes
has always been a challenging frontier for endoscopists since a long time. Per-oral
cholangioscopy (POCS) using miniature endoscope, through the channel of a stan-
dard duodenoscope, was rst described more than 40years ago in the 1970s [1, 2].
The procedure never became popular because of fragile instruments, poor image
quality, prolonged procedure time and the need for two trained endoscopists.
Over the past two decades, technological advancements have overcome many of
these issues, and per-oral cholangiopancreaticoscopy (POCPS) or direct cholan-
gioscopy, as it is popularly known, is fast establishing itself as an indispensable tool
for pancreatico-biliary diseases [3, 4]. This article reviews the basic concepts of
cholangioscopy, its utility and current status in literature.
2.2 Equipment andTechniques
Cholangioscopy can be done using video endoscope-based systems, which are the
traditional ‘mother–baby’ scopes, or the commonly used catheter-based systems
(SpyGlass, Boston Scientic). The above-mentioned systems are classied under
indirect per-oral cholangioscopy (iPOC) methods, as the visualization is retrograde
as in ERCP.
In patients with dilated bile ducts, direct per-oral cholangioscopy can be done
using ultra-slim endoscopes.
S. Bhatia
Department of Gastroenterology, Paras Hospital, Gurgaon, Haryana, India
S. Sud · R. Sud (
*)
Institute of Digestive and Hepatobiliary sciences, Medanta–The Medicity, Gurgaon, Haryana, India

18
2.3 Video Cholangioscope: Mother–Baby Systems
These systems comprise of a standard mother duodenoscope; through the accessory
channel of this mother scope, a miniature daughter or baby cholangioscope is passed
inside the bile duct [5]. The daughter scope is an ultra-slim video cholangioendo-
scope (CHF-B260; Olympus, Tokyo, Japan) with an outer diameter of 3.4mm. This
scope is passed through the accessory channel (4.2mm) of regular duodenoscope
(Fig.2.1) [6, 7].
The baby scope or cholangioscope has an accessory channel of 1.2mm, which is
used for irrigation during the imaging. The whole system requires two endoscopists,
one each for operating the mother and baby endoscopes, respectively. The insertion
of the baby scope into the bile duct is facilitated by doing a papillotomy. The chol-
angioscope is then inserted into the duodenoscope channel usually over a guide-
wire, and is advanced into the bile duct using the elevator. This is the crucial
procedural step as the chances of damage to the tip of cholangioscope are maximum
here. The use of a guidewire usually minimizes this damage [6, 7].
The primary shortcomings of these systems were the need for two trained endos-
copists, fragile instruments, the cost of the endoscopes, lack of separate air and
irrigation channels and limited scope tip deection [8, 9].
The clear advantage of video endoscope was the image quality, which was of
high-denition (HD) quality, and provision to use narrow-band imaging (NBI) tech-
nology to delineate tumour tissue [9]. However, this advantage was offset by previ-
ously mentioned shortcomings. Many of these limitations were addressed by the
next-generation single-operator cholangioscope.
Fig. 2.1 Two operator
video–cholangioscope
‘Mother–Baby’
endoscopes
S. Bhatia et al.

19
2.4 Single-Operator Cholangioscopy:
Catheter-Based System
Catheter-based systems are in principle based on mother–baby scope concept. A
commercial catheter-based cholangioscope—SpyGlass Direct Visualization System
or now known as the ‘legacy’ system (Boston Scientic, MA, USA)—was intro-
duced in 2007 as a rst single-operator cholangioscopy platform (Fig.2.2). This
system successfully addressed the limitation of traditional video endoscopes [9–11].
The cholangioscope (spy scope) was a 10-Fr-diameter catheter with four lumens. A
0.9-mm channel, which allowed the passage of a reusable optical probe (spy probe),
two separate 0.6-mm irrigation channels and a 1.2-mm working channel to allow a
slim biopsy forceps for visually targeted biopsies (spy-bite) or a laser/electrohy-
draulic (EHL) lithotripsy probe for therapeutic applications. The scope had four-
way tip deection allowing 70-degree view in up–down deection and a limited
30-degree view on right–left deection. The probe was connected to a proprietary
light source and a colour image sensor camera. The scope is inserted through the
accessory channel of a standard duodenoscope, usually over a guidewire, into the
biliary tree. This system had multiple advantages such as single- operator function;
separate channels for irrigation; four-way tip deection; and improved manoeu-
vrability and was partially disposable [7, 11, 12]. Owing to its advantages, the sys-
tem did become popular in clinical practice with a large amount of published
literature on its utility and potential uses [7, 10–12]. The system was not without its
limitations, primarily being the image quality. The image quality was the same and
SpyScope
tip with
Spybite
SpyProbe
SpyScope
Fig. 2.2 First generation
single operator
cholangioscope (SpyGlass,
Boston, scientic)
2 Cholangiopancreaticoscopy: A Distinct Diagnostic and Therapeutic Tool…

20
no better than the previous systems, a complete 360-degree view was a challenge,
and image quality used to deteriorate after a few uses of the spy probe [7, 9, 11].
Most of these disadvantages were overcome with the launch of a second-
generation SpyGlass DS system in 2015, with digital imaging capabilities. The new
scope has an integrated CMOS (complementary metal–oxide–semiconductor)
image sensor at the tip of scope, obviating the need for a separate spy probe (Figs.2.3
and 2.4). This produces much-improved digital quality images (Fig. 2.5) with a
wide-viewing angle. In addition, the new scope has a tapered tip and better
Fig. 2.3 Second
Generation digital single
operator cholangioscope
(SpyGlass DS, Boston
Scientic)
Fig. 2.4 Second generation digital SpyGlass scope with accessories
S. Bhatia et al.

21
ergonomics and is a single-use disposable catheter which ensures that there is no
image degradation as was a problem with the ‘legacy’ system [13].
With better imaging and improved ergonomics, the new single-operator endo-
scopes are getting popular in clinical practice. However, as this endoscope was
introduced recently, the data about its advantages and disadvantages is awaited.
There is robust data on application and utility of the rst-generation ‘legacy’ system
in literature.
2.5 Direct per-Oral Cholangioscopy
Direct bile duct visualization by a single operator can be achieved by using ultra-
slim, forward-viewing endoscopes in patients with dilated bile ducts [14, 15]. These
scopes are 5–6mm in diameter and were originally designed for transnasal or pae-
diatric endoscopies.
The major limitations are difculty in accessing the bile duct, looping of the
scope in the stomach, difculty to maintain position inside the bile duct and need for
presence of a dilated duct.
Normal hilar bifurcation. Benign stricture. CBD stones
Normal hilar bifurcation. HilarCholangioca. CBD stone
a
b
Fig. 2.5 Comparison of image quality of rst generation and Digital spyglass cholangioscopes.
(a) First generation Spyglass cholangioscopy images. (b) Spyglass DS (DIGISPY) cholangios-
copy images
2 Cholangiopancreaticoscopy: A Distinct Diagnostic and Therapeutic Tool…

22
Usually, the endoscope is advanced over a previously placed guidewire during
ERCP.The slim endoscope is then backloaded over the guidewire into the bile duct
[15]. A sphincterotomy is usually required for access due to large diameter of the
endoscope. Maintaining the guidewire and endoscope position is technically chal-
lenging, and a number of techniques including use of inated intraductal balloons
and use of an overtube have been described with good clinical success [16, 17].
2.6 Indications
The major indications and application of cholangioscopy are to manage difcult
biliary stones and to establish diagnosis in indeterminate biliary strictures.
There are a host of other indications and therapeutic applications of cholangio-
pancreaticoscopy in today’s endoscopy practice. These include the following.
Major clinical applications:
1. Establish the diagnosis in indeterminate biliary strictures.
2. Intraductal lithotripsy for large or impacted stones.
Other applications:
3. Pancreatic lithotripsy.
4. Evaluation of pancreatic cystic lesions.
5. Staging and extent of intraductal extension of periampullary carcinoma and
cholangiocarcinoma.
6. Mirizzi’s syndrome.
7. Evaluation of haemobilia.
8. Evaluation of unexplained biliary lling defects.
9. Retrieval of proximally migrated biliary or pancreatic stents.
10. Guidewire placement across difcult strictures.
11. Transpapillary drainage of the gallbladder.
12. Intraductal ablative therapies.
13. Primary sclerosing cholangitis.
2.7 Application andEfcacy
2.7.1 Intraductal Lithotripsy
Cholangioscopy-guided lithotripsy-using electrohydraulic (EHL) or laser litho-
tripsy (LL) probes in difcult biliary stones, which could not be removed by con-
ventional ERCP, have been well documented in the literature [18–22].
Stone fragmentation under direct vision of a cholangioscope is an exciting appli-
cation, especially where conventional methods have failed. Both biliary and
S. Bhatia et al.

23
pancreatic stones can be targeted by this modality without damaging the ductal
wall. Commercial EHL and LL probes are available which can be inserted through
the working channel of the cholangioscope and be used for stone fragmentation.
The EHL probe comprises of two coaxial electrodes at the probe tip. Under water
immersion, these produce high-energy hydraulic waves that lead to stone fragmen-
tation. Similarly, in laser lithotripsy, a quartz laser bre produces repetitive laser
energy beams, which gets converted to a high-amplitude mechanical shock wave
causing stone fragmentation [23].
2.7.2 Bile Duct Stones
Cholangioscopic intraductal lithotripsy using EHL or LL has been documented to
be a very successful modality for difcult biliary stones, where conventional meth-
ods like mechanical lithotripsy, use of balloon sphincteroplasty followed by basket
or balloon extractor have failed. The success rate has been consistently reported to
vary between 80% and 100% [11, 18–22]. A multicentre trial with the single-
operator cholangioscope system of 297 patients with biliary diseases reported more
than 92% success rate with EHL in 66 difcult biliary stones, with complete ductal
clearance achieved in over 70% of patients in the rst session [22]. Another smaller
study of 26 patients, 12 of whom had failed mechanical lithotripsy, showed 100%
successful ductal clearance with EHL [21].
Laser lithotripsy (Fig.2.6) has been shown to be equally effective as compared
with EHL.A study from India included 64 patients with difcult biliary stones had
100% success of laser lithotripsy with >83% bile duct clearance in the rst session
itself [21]. In another multicentre trial, 97% patients were successfully treated with
Fig. 2.6. Intraductal laser
lithotripsy
2 Cholangiopancreaticoscopy: A Distinct Diagnostic and Therapeutic Tool…
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