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Acute Appendicitis
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AndreaPakula andRubySkinner
1 Introduction
Appendectomy for acute appendicitis is one of the most commonly performed sur­gical procedures for acute care surgeons. The estimated lifetime risk for acute appendicitis is 7–8%, and there are approximately 300,000 patients diagnosed with acute appendicitis in the United States. Luminal obstruction of the appendix is com­monly causative of appendicitis, and this obstruction can be related to a fecalith, impacted stool, or lymphoid hyperplasia [1, 2].
Surgical approaches to appendectomy have evolved from open surgery to mini­mally invasive approaches. Kurt Semm performed the rst laparoscopic appendec­tomy in September 1980, and with the subsequent evolution of the minimally invasive technology, an open appendectomy is not frequently done in the adult populations [3].
In a 2010 meta-analysis of randomized controlled trials comparing minimally invasive to open appendectomy, it was determined that laparoscopy offers signi­cant advantages over open appendectomy to include less pain, a lower incidence of surgical site infection, a decreased length of hospital stay, an earlier return to work, a lower overall cost, and better quality of life scores. This was an early study docu­menting the superiority of the minimally invasive approach based on high strength studies that allowed for the strong recommendation of the laparoscopic approach for both uncomplicated and complicated acute appendicitis [4].
Similarly, in a more recent 2017 meta-analysis comparing laparoscopic versus open appendectomy in cases of complicated appendicitis, laparoscopy
A. Pakula (*) Adventist Health Simi Valley Hospital, Simi Valley, CA, USA e-mail: pakulaam@ah.org
R. Skinner St. Bernadine’s Medical Center, San Bernadino, CA, USA e-mail: ruby.skinner@commonspirit.org
© The Author(s), under exclusive license to Springer Nature Switzerland AG 2023 F. Coccolini et al. (eds.), Mini-invasive Approach in Acute Care Surgery, Hot Topics in Acute Care Surgery and Trauma,
https://doi.org/10.1007/978-3-031-39001-2_5
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demonstrated less surgical site infections, reduced time to oral intake, and length of hospitalization. There was no signicant difference in intra-abdominal abscess rates. Operative time was longer for laparoscopy but did not reach statistical signi­cance in the RCT subgroup analysis [5]. Overall, laparoscopy for appendectomy is safe and can be applied in traditionally high-risk populations. Laparoscopy is safe for patients with obesity, the elderly population with medical comorbid conditions, and pregnant patients in all trimesters [69].
The adoption of robotic-assisted laparoscopic techniques has become more prev­alent in general surgery, and approaches to acute care cases are evolving [10, 11]. The adoption of robotic-assisted laparoscopic appendectomy into the surgical arma­mentarium of the acute care surgeon is also feasible.
A. Pakula and R. Skinner
2 Preoperative Diagnosis andIndications forSurgery
Patient presentation can vary from minimal symptoms with vague lower abdominal pain to more localized pain with or without peritoneal inammation. The classic physical exam ndings and patient complaints are described as periumbilical pain that radiates and ultimately localizes to the right lower quadrant. If the appendix is more anterior and adjacent to the parietal peritoneum, patients will have focal ten­derness on palpation. If the appendix is located in the retrocecal position, physical exam ndings may not be as clear. Common laboratory ndings include leukocyto­sis and an elevated c-reactive protein. Though imaging is not always necessary, ultrasound is recommended in pregnant or pediatric patients, and computed tomog­raphy (CT) of the abdomen and pelvis is the preferred diagnostic study in adults. In the 2016 ACS NSQIP database, CT scan was shown to have higher positive predic­tive values compared to ultrasound (US) and MRI [12]. CT is specically useful in identifying a periappendiceal phlegmon or abscess if the duration of symptoms is questionable. The utilization of imaging or modality selected is based on physician preference and condence in the diagnosis.
3 Operative Technique forLaparoscopic
andRobotic Appendectomy
Prior to making skin incisions, local anesthesia can be injected into the skin. The rst step is to then gain access to the peritoneal cavity. This can be done using a Veress needle, open/Hassan, or optical view entry technique. Port placement for laparoscopic appendectomy relies on triangulation of instruments to the right lower quadrant. Selection of port size is surgeon preference, but at least one 12mm port is needed if an endoscopic stapler is to be used. For the robotic-assisted approach, either three 8mm or two 8mm and a 12mm cannula are used. Again, the 12mm port is necessary to accommodate the stapler if this is the chosen technique. There are some variations to port placement utilizing the robotic approach which are shown in (see Figs. 1 and 2) Fig. 2a, b. Once ports have been placed and
a
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Fig. 1 Laparoscopic port placement
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b
Fig. 2 Robotic assisted port placement
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Fig. 3 Creation of mesenteric window
A. Pakula and R. Skinner
pneumoperitoneum is achieved to 15mmHg, the patient is placed in Trendelenburg position and rotated left side down. The operation begins with initial exploration to identify any unexpected pathology. Atraumatic graspers are then inserted, and the rst step is to identify the appendix. This can sometimes be difcult so identifying the cecum can help to facilitate this step. The ligament of Treves located on the distal ileum near the ileocecal valve can also be used to locate the appendix. During acute appendicitis, it is often adherent to the mesoappendix or the appendix itself. The omentum and small bowel are gently swept away from the right lower quadrant. The appendix can be found lateral to the ileal cecal valve at the base of the taenia. If the appendix is in the retrocecal position, the cecum will need to be mobilized medi­ally by dividing the white line of Toldt in order to expose the appendix. The prin­ciples of mesenteric division as well as division of the appendix are similar regardless of the minimally invasive approach. Once identied, the appendix can be gently grasped taking care not to cause rupture. The mesoappendix should be identied, and either a window can be created at the base of the appendix using a dissector or the mesoappendix can be divided moving distally to proximally (Fig. 3). The win­dow would allow for hemoclips, a suture, or an endoscopic stapler to be used to control the mesoappendix vessels. Alternatively, an energy device such as the ultra­sonic scalpel, advanced bipolar energy, simple bipolar, or monopolar energy can be used to divide the mesoappendix which contains the appendiceal artery.
There are several different techniques for dividing the appendix itself, and this depends on surgeon preference as well as the characteristics of the appendiceal tis­sue. These include stapled division, suture ligation, or placement of an Endoloop with or without dunking of the appendiceal stump. The robotic technology facili­tates suturing, though this can be done laparoscopically as well. If a stapler is used, a short-height load (2.0–3.0mm) is typically chosen to seal the mesoappendix and artery, and a medium height staple load (2.5–3.5mm) is often used to divide the appendix itself (Fig. 4). Once divided, the staple lines are inspected to assure there
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Fig. 4 Division of base of appendix with stapler
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is no bleeding or leakage of stool. Next the appendix can be placed in a retrieval bag and removed through the larger port. If there is evidence of contamination, this can be judiciously irrigated and suctioned. Once the procedure is complete, the ports are removed, and the fascial incision at any port site larger than 5mm is closed to pre­vent hernia formation. This is usually done with a 0-vicryl suture. Skin incisions are then closed, and sterile dressing or skin glue is applied.
4 Complicated Appendicitis
In patients who present with signs and symptoms consistent with appendicitis and demonstrate evidence of perforation with phlegmon or abscess on preoperative imaging, immediate surgical intervention is not always recommended. If the patient is not septic requiring immediate surgical exploration, they are admitted to the hos­pital, started on IV antibiotics, and treated nonoperatively, which may or may not include radiology-guided drain placement to control the infection depending on the location and size of the phlegmon or abscess. These patients can then go on to undergo appendectomy in 6–8weeks after resolution of acute inammatory changes and drainage of the abscess. 25% of appendectomies performed each year are due to complicated appendicitis [13].
5 Conclusion
Appendectomy for acute appendicitis is one of the most common procedures per­formed by acute care surgeons, and minimally invasive approaches are standard. Laparoscopy in general is associated with signicant clinical benets and overall cost benets for patient care, and patients with acute appendicitis are afforded with
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A. Pakula and R. Skinner
those benets. High-risk populations including elderly patient, those with obesity, and pregnant patients, all can safely be managed with laparoscopy for acute appen­dicitis. Finally, robotic-assisted appendectomies are being performed; although the literature is sparse for this application, there are evolving benets reported of apply­ing robotic surgery for common acute care surgical emergencies.
References
1. Stewart B, Khanduri P, McCord C, etal. Global disease burden of conditions requiring emer­gency surgery. Br J Surg. 2014;101:e9–e22.
2. Bhangu A, Soreide K, Di Saverio S, etal. Acute appendicitis: modern understanding of patho­genesis, diagnosis , and management. Lancet. 2015;383:1278–87.
3. Meljnikov I, Radojcic B, Grebeldinger S, Radojcic N.History of surgical treatment of appen­dicitis. Med Pregl. 2009;62(9–10):489–92.
4. Li X, Zhang J, Sang L, et al. Laparoscopic versus conventional appendectomy—a meta­analysis of randomized controlled trials. BMC Gastroenterol. 2010;10:129.
5. Athanasiou C, Lockwood S, Markides GA.Systematic review and meta-analysis of laparo­scopic versus open appendicectomy in adults with complicated appendicitis: an update of the literature. World J Surg. 2017;41(12):3083–99. https://doi.org/10.1007/s00268- 017- 4123- 3.
6. Werkgartner G, Cerwenka H, El Shabrawi A, etal. Laparoscopic versus open appendectomy for complicated appendicitis in high risk patients. Int J Color Dis. 2015;30:397–401.
7. Wang D, Dong T, Shao Y, etal. Laparoscopy versus open appendectomy for elderly patients, a meta-analysis and systematic review. BMC Surg. 2019;19:54.
8. Michailidou M, Sacco Casamassima MG, Goldstein SD, et al. The impact of obesity on laparoscopic appendectomy: results from the ACS National Surgical Quality Improvement Program pediatric database. J Pediatric Surg. 2015;50:1880–4.
9. Lee SH, Lee JY, Choi YY, etal. Laparoscopic appendectomy versus open appendectomy for suspected appendicitis during pregnancy: a systematic review and updated meta-analysis. BMC Surg. 2019;19:41.
10. Certulo LN, Harmon K, Ortiz J, etal. Case report of a robotic-assisted laparoscopic repair of a giant incarcerated recurrent inguinal hernia containing bladder and ureters. Int J Med Robot. 2015;1:15–7.
11. Cengiz TB, Aghayeva A, Atasoy D, etal. Robotic TAPP repair of incarcerated femoral hernia with utilization of indocyanine green dye—a video vignette. Color Dis. 2017;19(8):186.
12. Agathis AZ, Miller M, Divino CM.National trends in diagnostic imaging for appendicitis: a cross-sectional analysis using NSQIP.Am Surg. 2019;85(6):625–30.
13. Perez KS, Allen SR.Complicated appendicitis and considerations for interval appendectomy. JAAPA. 2018;31(9):35–41.
Acute Cholecystitis andEmergency
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Common Bile Duct Exploration
SimoneFrassini, PaolaFugazzola, MatteoTomasoni, andLucaAnsaloni
1 Background
1.1 Anatomy andPhysiology
The gallbladder is a small hollow organ attached to the inferior surface of the liver, and it is divided into four components: neck, infundibulum, body, and fundus [1] (Fig.1).
The gallbladder function is to store and concentrate the bile synthesized by the liver—from 30 to 60mL per day—as an extrahepatic reservoir. Vagal stimulation and release of cholecystokinin from neuroendocrine cells in the duodenum, in response to the presence of the fat in the diet, cause gallbladder contraction and the transport of the bile down along the cystic duct [2].
The cystic duct drains into the common bile duct forming typically an acute angle and can range from 1 to 5cm in length: there are several uncommon anatomic variations in cystic duct anatomy, and knowledge of these variations is important to avoid possible injury to the biliary tree during surgery.
Above the cystic duct lies the common hepatic duct, draining the left and the right hepatic duct system: after the conjunction with the gallbladder, the common bile duct descends behind the rst part of the duodenum and passes through the
S. Frassini (*) · L. Ansaloni General Surgery I Unit, Fondazione IRCCS Policlinico San Matteo, University of Pavia, Pavia, Italy
Department of Clinical, Surgical, Diagnostic and Pediatric Sciences, Università degli Studi di Pavia, Pavia, Italy e-mail: simone.frassini01@universitadipavia.it; l.ansaloni@smatteo.pv.it
P. Fugazzola · M. Tomasoni General Surgery I Unit, Fondazione IRCCS Policlinico San Matteo, University of Pavia, Pavia, Italy e-mail: p.fugazzola@smatteo.pv.it; m.tomasoni@smatteo.pv.it
© The Author(s), under exclusive license to Springer Nature Switzerland AG 2023 F. Coccolini et al. (eds.), Mini-invasive Approach in Acute Care Surgery, Hot Topics in Acute Care Surgery and Trauma,
https://doi.org/10.1007/978-3-031-39001-2_6
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Spiral part of cystic duct
tmann’s pouch)
Descending (2nd) par
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Neck of gallbladder
Body (corpus) of gallbladder
S. Frassini et al.
Right hepatic duct
Left hepatic duct
Common hepatic duct
Infundibulum (Har of gallbladder
Smooth part of cystic duct
Fundus of gallbladder
t of duodenum
Gland openings
Major duodenal papilla (of Vater)
Common bile duct
Pancreatic duct
Ampulla (of Vater)
Fig. 1 Anatomy of gallbladder and the biliary tract
pancreas head forming the intrapancreatic portion of the biliary tree. The pancreatic duct also joins the common bile duct on its distal part, composing the ampulla of Vater and nally going within the wall of the third part of the duodenum to release its content. Rarely, the common bile duct and the pancreatic duct may have a sepa­rate course encompassed by the head of the pancreas with two separate orices in the duodenum (Figs.2 and 3).
1.2 Pathogenesis
Acute cholecystitis is an acute inammatory process involving the gallbladder, mainly attributable to the presence of gallstones but also due to other factors such as ischemia, motility disorders, direct chemical injury, infections, collagen disorders, and allergic reactions. In a recent survey in the United States, over 10% of patients with gallstone-related complications have a rst clinical presentation with acute calculous cholecystitis (ACC) [3, 4]. The pathological process of acute cholecystitis is an obstruction of the neck or in the cystic duct by a gallstone with two factors determining the progression and the severity of the disease: the degree of obstruc­tion and the duration of obstruction. When the obstruction is of short duration and partial, the patients can experience biliary colic; otherwise, when the obstruction is complete and of long duration, the patients can develop acute cholecystitis, and more serious septic complications can occur. Possible complications when gallstone­related ACC is ignored or misdiagnosed are acute cholangitis, acute biliary
Joining
Joining
left side
n
left side
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Figs. 2 and 3 Possible anatomic variations of biliary tract tree
common
hepatic duct
Low union
with common
hepatic duct
Joining
gallbladder
Adherent to
common
hepatic duct
Joining cystic
duct
High union with
common bile duct
Two accessory
hepatic ducts
common
hepatic duct
pancreatitis, gallstone ileus, Mirizzi syndrome, gallbladder carcinoma, and porce­lain gallbladder [5]. According to the most recent evidence, the pathogenesis of ACC goes through a four-step classication:
1. Edematous cholecystitis (0–4days): rst reactive pathological phase, with inter-
stitial uid and parietal edema but tissues are intact without deeper layer involvement.
2. Necrotizing cholecystitis (3–5 days): gallbladder has edematous changes with
areas of necrosis and local hemorrhage. There are portions of scattered necrosis, but they are supercial and do not involve the full thickness of the wall.
3. Suppurative cholecystitis (7–10days): the active repairing process of inamma-
tion is evident. The gallbladder wall is thickened by brous proliferation, and pericholecystic abscesses are present.
Cystic duct
absent or
very short
Anterior spiral
joining common
hepatic duct on
Posterior spiral joining commo hepatic duct on
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4. Chronic cholecystitis: it occurs after repeated occurrence of mild cholecystitis
attacks and consequently brotic or atrophic process in the gallbladder wall.
With the obstruction of a tubular structure as the cystic duct, pain may come from increased intraluminal pressure, and it precedes infectious complications due to the biliary stasis.
S. Frassini et al.
1.3 General Consideration
1.3.1 Symptoms
The three most common symptoms associated with the biliary disease are resumed by the “Charcot triad”: right upper quadrant pain, fever, and jaundice.
• PAIN: when the gallbladder lumen cannot fully empty due to obstruction by a
stone, pain bers are activated resulting in a typical abdominal pain in the epigas-
trium or the right upper quadrant. From a weak and occasional postprandial pain,
in case of severe ACC, the clinical condition can evolve to abdominal tenderness
and Murphy’s sign. A recent paper, including 17 studies about clinical assess-
ment of ACC, showed a positive likelihood ratio for right upper quadrant tender-
ness and Murphy’s sign in the diagnosis of acute cholecystitis [6].
• FEVER: this symptom is a common systemic manifestation of infection or
inammation of the biliary tract. In case of fever associated with common right
upper quadrant pain, ACC or even cholangitis must be immediately suspected.
• JAUNDICE: a serum bilirubin level of 2.5mg/dL or even more is necessary to
detect scleral icterus; levels above 5mg/dL will cause cutaneous jaundice. Fever,
right upper quadrant pain, and jaundice suggest generally a blockage of biliary
secretion due to gallstones but could be also secondarily to other less common
origins. Jaundice is typically related to surgical, from obstruction, or medical,
from hepatocellular disease, cause.
1.3.2 Laboratory Test
When a biliary alteration is suspected, the routine hepatic panel of blood test is mandatory as a rst-level diagnostic tool. Determination of the conjugated or unconjugated level of bilirubin, alkaline phosphatase, and serum transaminases is useful to detect and discriminate a hepatic or cholestatic source of the pathological process.
In addition, in the case of ACC, also phlogistic signals in the blood exams must be checked out: white blood cells count (WBC), C-reactive protein (CRP), and pro­calcitonin (PCT) increase when infection or inammation are evolving, and they represent also a key component of all the existing diagnostic score.
1.3.3 Imaging
• Ultrasound (US): Transabdominal ultrasound is an inexpensive, sensitive, accu-
rate, and reproducible test—when in expert hands—to evaluate the gallbladder