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Section I • General Principles

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. Table5.1 Advantages and Disadvantages of Open and Closed-Suction Drains
Open drain Closed-suction drain
Advantages Generates pathways for bulky or viscous
Disadvantages Retrograde infection More vulnerable to obstruction by small
Closed Suction, Active Drains
Jackson-Pratt and Blake drains (. for closed-suction systems. e Jackson-Pratt drain is oval-shaped with numerous orices and intraluminal corrugations (inlay). e Blake drain has four channels along the sides with a solid core center. In contrast to passive drains, active or suction drains maintain a negative pressure gradient.
material
Lowers risk of mechanical erosion and pressure necrosis
Fig. 5.2
) are commonly used radiopaque, silicone products
Lowers risk of retrograde infection
Accurate measurement of drainage
Facilitates radiographic studies Skin pro­tection from irritating discharge
tissue fragments or ingrowth of surround­ing tissue
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. Fig.5.2
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Chapter  • Principles of Drainage
Sump Drains

Sump drains (. inow “sump” lumen. e larger lumen is connected to a suction system and evacuates intra­abdominal secretions. e smaller lumen serves as a venting tube, allowing air to enter the larger lumen. is principle should help to break the vacuum in the large draining tube, maintaining the drain in a productive patent state, without the surrounding tissues continually occluding the drainage holes in the tube. Sump drains are oen used when large uid volumes or more particu­late or thick collections have to be evacuated. e occlusion of the smaller venting tube by tissue debris due to retrograde inow demonstrates a potential disadvantage of sump drains that occurs especially when the suction is disconnected. Some sump drains have an additional third lumen that allows the instillation of a lavage solution.
. Fig.5.3
Fig. 5.3
) are usually double-lumen tubes with a larger outow lumen and a smaller
Complete Drainage System
Collapsible devices connected to the drain tubes generate automatically a negative pressure gradi­ent and keep the system “sealed”, which is believed to have resulted in a substantial decrease in retrograde infections (
. Fig.5.4
. Fig. 5.4).
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Section I • General Principles
Prophylactic Drainage
Drain Orifice
e drain exit site through the skin is created by a penetrating cut with a scalpel (. Fig. 5.5a). A Kelly clamp is inserted into the orice ( (.
Fig. 5.5c
). e underlying hand prevents bowel injury. is technique creates a tunnel that helps to seal the abdominal cavity aer drain removal. Aer clamping the drain tip, the Kelly clamp and drain are pulled through the abdominal wall from inside outwards (. Fig. 5.5d). Others prefer to create the tunnel from inside out and pull the drain into the abdomen. Finally, the drain position is secured by a non-reactive skin suture, and the drain tube is connected to the suction device.
. Fig. 5.5b) and penetrates the abdominal wall diagonally
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. Fig.5.5
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Chapter  • Principles of Drainage

Prophylactic Drains
Prophylactic drainage aer upper abdominal operations is used to evacuate intra-abdominal uid that may develop, such as ascites, blood, chyle, bile, pancreatic, or intestinal juice, that are either harmful/toxic for adjacent tissue or might become infected. erefore, drains are placed in spaces that tend to accumulate uid, such as the subhepatic (1), right subphrenic (2), le subphrenic (3), and parapancreatic (4) spaces (. Fig. 5.6).
. Fig.5.6
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Section I • General Principles
Perianastomotic Drains
Another proposed function of prophylactic drainage is the early detection of anastomotic leak­age. If drains are to be used near a high-risk anastomosis, they should not be placed in direct contact with the anastomosis, but, rather, with a safety margin in between to prevent drain-related erosions. is principle is illustrated for a biliodigestive anastomosis, where the drain is placed posterior to the anastomosis (
Although routine use of prophylactic drainage was oen considered necessary to prevent complications, there is growing evidence that this practice may be associated with adverse eects. Retrograde drain infections or drain-related complications are known adverse eects. Several randomized, controlled trials are available investigating the routine use of prophylactic drainage for selected procedures (
. Fig. 5.7).
. Table 5.2).
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. Fig.5.7
. Table5.2 Evidence-based Recommendations for Prophylactic Drainage Practice
Gastrointestinal surgery Procedures Evidence-based
Hepato-pancreatico-biliary Hepatic resection without
biliodigestive anastomosis
Cholecystectomy (open, laparoscopic)
Pancreatic resection Controversial
Biliodigestive anastomosis NA
Upper GI tract Esophageal resections Intrathoracic drain for any
Total gastrectomy Controversial
Distal gastrectomy No drain
Roux-en-Y gastric bypass No drain
Duodenotomy with omental No drain
patch for duodenal perforation
recommendation
No drain
a
No drain
b
approach
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NA, not assessed
a
Only one randomized controlled trial in pancreatic cancer
b
Controversial even in centers where a prospective randomized trial suggested no benet
Chapter  • Principles of Drainage

Therapeutic Drainage
Predisposed Spaces for Collections
Infected collections, such as abscesses or infected bilomas, are known complications aer upper abdominal surgery and require drainage by operative or radiologically guided drain placement. e right subphrenic space (1), le subphrenic space (2), Morison’s pouch (3), le subhepatic space (4), and omental sac (5) are anatomic spaces that predispose to abscess development (. Fig. 5.8).
. Fig.5.8
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Section I • General Principles
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
Catheters
e majority of postoperative collections in the upper abdomen are manageable by means of percutaneous drainage by interventional radiologic techniques using standard aseptic technique and local anesthesia. ereby, collections are drained percutaneously under ultrasonographic or CT guidance using the Seldinger or trocar techniques. is gure illustrates a typical percutaneous drainage catheter, the MAC-LOC (. Fig. 5.9a) that can be inserted by the introduction cannula (
. Fig. 5.9b) or the trocar stylet (. Fig. 5.9c). e catheter has large, oval side ports to increase
the drainage capability, as well as a radiopaque band that identies the proximal area of the loop. is type of “self-locking” loop catheter has “memory” to prevent later displacement, i. e., the loop at the end can be straightened during insertion by introducing a stylet intraluminally. Aer the catheter is positioned in place, the stylet is removed, and the loop reforms.
Some uid collections may require surgical drainage with repeated abdominal lavage and second-look procedures (. Table 5.3).
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. Fig.5.9
. Table5.3 Criteria for Percutaneous and Surgical Drainage of Infected Collections
Percutaneous drainage Surgical drainage
Unilocular collection/abscess Multilocular collections/abscesses
Low viscosity of drain uid Multiple, non-communicating collections
Drain route not traversing intra-abdominal organs
or thorax
Tricks of the Senior Surgeon
Whenever indicated, always use closed drain systems and keep drains as short as possible to
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minimize the risk of retrograde infections.
Place drains near but never in direct contact to the anastomotic sutures to prevent drain-
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induced erosions or drain-induced anastomotic leaks.
When drains are not productive, do not rely on them! Drains could be occluded or obstructed
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by tissue despite an adjacent uid collection.
Try to position intraperitoneal drains such that the drain does not rub against or lie in direct
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contact with blood vessels or hollow organs in an attempt to prevent drain erosions.
These drains often can be manipulated and positioned better under uoroscopic guidance
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by interventional radiologists.
Drains may not eectively evacuate bleeding, especially when there are thick or older blood
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clots.
High viscosity of drain uid Percutaneous drain route traversing intra-abdominal organs or thorax

Surgical Energy Devices or Devices for Hemostasis

Lukasz Filip Grochola, René Vonlanthen
Surgical Devices: Hemostasis, Sealing, and Dissection
Surgical energy devices that provide adequate hemostasis and allow accurate dissection of tissue are essential during surgical procedures. Unreliable tools can lead to bleeding, cause injury to adjacent organs, and jeopardize visualization. Modern energy devices have seen a rapid develop­ment in the past few years, leading to a striking improvement in both the control of hemostasis and the precision of tissue dissection, therefore minimizing operation time, collateral damage to surrounding tissue, and blood loss, and resulting in strikingly improved outcomes in both lapa­roscopic and open surgical procedures.
Requirements for surgical energy devices
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In general, an energy surgical device used for control of hemostasis, sealing, and tissue dissection should fulll the following requirements in order to enable safe and ecient surgery:
Provide reliable hemostasis
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Minimize collateral damage to surrounding tissue
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Permit fast dissection of tissue to minimize operation time
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Provide exibility in usage allowing unrestricted access to the operating eld
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Be easy to handle by trained sta
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Be cost-eective
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ere are ve types of widely used general surgical devices:
1. Basic energy-based devices: Instruments that utilize high-frequency monopolar or bipolar electric current to cut or coagulate biologic tissue. ey lack highly sophisticated additional technical features designed to improve the control of dissection and hemostasis.
2. Advanced energy-based devices: Tools that utilize bipolar or ultrasonic energy combined with sophisticated features, such as tissue sealing mechanisms, temperature feedback control, and other features designed to control lateral thermal spread for simultaneous tissue dissection and hemostasis control.
3. Argon plasma coagulator (APC): A noncontact monopolar electrocoagulation device designed to deliver a high-frequency current through a jet of ionized argon gas for the purpose of he­mostasis control.
4. Topical hemostatic/sealant devices: Assist in the control of diuse oozing and minor bleeding. Provide hemostasis by contact activation of coagulation or induction of the last steps of the coagulation cascade, mechanical tamponade, or synthetic sealing.
5. Clips: Provide fast and reliable vessel and tissue sealing by mechanical compression.
Overview of devices
Basic energy-based devices
Monopolar electrosurgery
Monopolar electrosurgery devices revolutionized surgery aer their development in the 1920s and are the mainstay of surgical dissection techniques and control of hemostasis. ey generate a high-frequency (HF) electrical current, which ows from the active electrode in the hand-piece
P.-A. Clavien, M. G. Sarr, Y. Fong, M. Miyazaki (Eds.), Atlas of Upper Gastrointestinal and Hepato-Pancreato-Biliary Surger y, DOI 10.1007/978-3-662-46546-2_6, © Springer-Verlag Berlin Heidelberg 2016
Section I • General Principles
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to the target tissue and subsequently through the patient to the passive electrode, grounding pad (
. Fig. 6.1, top; . Tab. 6.1). is ow heats the tissue and causes a small area of tissue to vaporize
through rapid tissue heating to temperatures reaching 400 °C (CUT mode) or coagulate through a slower heating process to temperatures approximating 100 °C (COAG mode). ose two modes are generated by distinct types of electrical current, which dier with regard to the wave form, frequency, and voltage. Monopolar current can be applied to the target tissue using a wide variety of surgical tips attached to a pencil-shaped hand-piece ( include the blade, eective in both the cutting and the coagulation of tissue; the Colorado needle (an ultrasharp tip), used for precise tissue dissection; the ball electrode for coagulation of a larger tissue area; and the monopolar forceps. In addition, the surgeon can choose dierent congura­tions of electrosurgical pencils, such as the rocker switch and push button congurations, as well as foot control pencils. Although monopolar electrosurgery is highly useful and eective, the surgeon should be aware of its potential safety hazards, such as unintended burns to the patient, malfunction of implanted electronic devices (e. g., pacemakers, cardioversion devices, sacral/spinal cord stimulators) or superheating of prosthetic conductive joints.
. Fig. 6.1, bottom, le to right). Such tips
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. Fig.6.1
Bipolar electrosurgery
Bipolar electrosurgery devices utilize an active and a return electrode, which are part of a single instrument, most oen a surgical forceps (. tool and only through the targeted tissue. is feature reduces lateral thermal spread and creates less smoke compared with monopolar equipment. However, this technology leads to less penetra­tion of current density, which can be a disadvantage for hemostasis in certain areas. e lateral thermal spread as well as the sticking of tissue debris can be further decreased by a bipolar forceps, which incorporates a water irrigation system that causes a cooling of the forceps tip as well as of the targeted tissue. is feature, as described in more details in useful in hemostasis control and dissection of liver parenchyma.
Fig. 6.2; . Tab. 6.1
). Current ows from one tip of the
Chap. 3, makes it particularly
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. Fig.6.2
Chapter  • Surgical Energy Devices or Devices for Hemostasis
Combined: ultrasonic,
pressure, bipolar
Pressure, bipolar,
integrated blade
Freq: 47 kHz Power: n.a.

Fastest dissection in class,
highest burst pressure,
relatively high prospen-
sity for collateral tissue
damage
Temperature is controlled
at tissue interface, low
lateral thermal spread;
optionally available with
additional monopolar tip
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integrated blade
Maxim. Power: 135 W Maxim. Power: 150 W Amp: 50–80 µm
Freq: 55 kHz
Maxim. Power 180 W Amp: 50–100 µm
Temperature is controlled
at tissue interface. Oset
electrode further reduces
lateral thermal spread
Fast dissection, high pros-
pensity for collateral tissue
damage
Cost-eective device,
optionally available with
integrated water irrigation
to cool down tip and
reduce lateral thermal
spread
. Tab.6.1
Yes Ye s Yes Ye s Ye s Yes
Yes Ye s Yes Ye s Ye s Yes
Device Monopolar pencil Bipolar forceps Harmonic ACE Enseal LigaSure Thunderbeat
Principle Monopolar Bipolar Ultrasonic Pressure, bipolar,
Sealing function Ye s Yes Yes Yes Ye s Yes
Transecting function Ye s Yes Ye s Yes Ye s Yes
Haemostasis
(w/o cutting)
Open + laprascopic
surgery
n.a. n.a. 450 mmHg 720 mmHg 615 mmHg 730 mmHg
(CUT) 200 W (COAG)
Burst pressure
Technical specications Maxim. Power: 300 W
(5–7 mm vessels)*
Lateral thermal spread ++++ ++ +++ + ++ +++
2–3 mm 2–3 mm 5 mm 7 mm 7 mm 7 mm
Maximum size
of vessel*
highest propensity for col-
lateral tissue damage
Tissue compression n.a. Not uniform Not uniform Uniform Not uniform Uniform
Comment Cost-eective device,
* approximate values