You are on page 1of 14

International Journal of Colorectal Disease

https://doi.org/10.1007/s00384-021-03940-8

REVIEW

Classification of acute appendicitis (CAA): treatment directed new


classification based on imaging (ultrasound, computed tomography)
and pathology
Jörg C. Hoffmann 1 & Claus-Peter Trimborn 1 & Michael Hoffmann 2 & Ralf Schröder 3 & Sarah Förster 4 & Klaus Dirks 5 &
Andrea Tannapfel 4 & Matthias Anthuber 2 & Alois Hollerweger 6

Accepted: 21 April 2021


# The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021

Abstract
Purpose Acute appendicitis (AA) is amongst the most common causes of acute abdominal pain. In spite of progress based on risk
stratifications, “negative” appendectomies are performed in up to 30% of patients whilst the appendix perforates in others.
Preoperative classification of AA based on imaging is therefore recommended. The aim was to classify AA based on imaging
(ultrasound/US, computed tomography/CT), surgical pathology, and/or histopathology in order to differentiate between com-
plicated and uncomplicated AA. A new classification of acute appendicitis (CAA) shall be illustrated by typical US and CT
images and be employed in a diagnostic and therapeutic algorithm.
Methods Medline, Embase, and the Cochrane Library were searched. Any study after 1970, which investigated clinical scores,
pathology, US, CT, magnetic resonance imaging, and treatment of AA, was included. Typical images were taken from the
author’s image database.
Results Five main types of AA are defined, normal appendix (type 0), nonvisualised appendix (type X), uncompli-
cated AA (type 1), complicated AA without perforation (type 2), and complicated AA with perforation (type 3). The
imaging modality is indicated by an additional letter, e.g., type p3b for free perforation on pathology. Standardised
reporting of the appendix evaluation by US and CT is presented, as well as algorithms for AA management.
Imaging features indicating imminent perforation, as well as likely recurrence, were both classified as complicated
AA.
Conclusion Imaging is mandatory in suspected AA. The CAA clearly separates uncomplicated from complicated forms of AA
allowing nonoperative management in selected patients with uncomplicated forms of AA.

Keywords Imaging . Complicated appendicitis . Uncomplicated appendicitis . Standardised reporting . Diagnostic algorithm .
Therapeutic algorithm

* Jörg C. Hoffmann 3
Radiologische Klinik, St. Marien- und St. Annastiftskrankenhaus
joerg.hoffmann@st-marienkrankenhaus.de Ludwigshafen, Ludwigshafen, Germany
4
Institut für Pathologie der Ruhr-Universität Bochum,
1
Medizinische Klinik I mit Schwerpunkt Gastroenterologie, Bochum, Germany
Diabetologie, Rheumatologie und Onkologie, St. Marien- und St. 5
Gastroenterologie, Allgemeine Innere Medizin und Geriatrie,
Annastiftskrankenhaus, Salzburger Straße 15, Rems-Murr-Kliniken Winnenden, Winnenden, Germany
D67067 Ludwigshafen, Germany 6
Abteilung für Radiologie und Nuklearmedizin Krankenhaus der
2
Klinik für Allgemein-, Viszeral- und Transplantationschirurgie, Barmherzigen Brüder Salzburg, Salzburg, Austria
Universitätsklinikum Augsburg, Augsburg, Germany
Int J Colorectal Dis

Introduction updated guideline on the diagnosis and treatment of AA by the


World Society of Emergency Surgery (WSES) recommend
Acute appendicitis (AA) is one of the most common causes of the use of clinical scores in order to exclude AA in nonpreg-
lower abdominal pain in patients presenting to the emergency nant patients [1, 4]. At the other end of the spectrum, the
room; AA is also the leading cause of peritonitis in young adults EAES and the WSES regard high scores as sufficient evidence
and children [1]. Whilst the gold standard of AA treatment is for the diagnosis of AA without need for further imaging.
appendectomy, the most frequent abdominal operation world- Such recommendations do not take into account the long list
wide, some evidence suggests that uncomplicated AA may as of alternative diagnoses which can cause lower abdominal
well be treated nonoperatively [1–3]. Furthermore, overdiagno- pain. Further, patients who did not have imaging studies for
sis of AA can lead to so called “negative” appendectomies. suspected AA had a more than threefold increased likelihood
Delay of the correct diagnosis, on the other hand, can lead to of “negative” appendectomies [14]. Furthermore, clinical
perforation. Therefore, both the correct diagnosis of AA in the scores certainly do not allow a distinction of complicated
first place and a distinction between complicated and uncom- and uncomplicated AA precluding nonoperative management
plicated forms of AA are important. The European Association [15]. To this end, some guidelines (e.g., the Dutch guideline of
of Endoscopic Surgery (EAES) defined complicated AA as 2010 or the EFSUM guideline of 2019) recommend imaging
gangrenous AA with or without perforation, AA with an in all patients with suspected AA [16–19].
intraabdominal abscess, and AA with periappendicular We herein propose a new classification of acute ap-
contained phlegmon or purulent/free fluid [4]. Consequently, pendicitis (CAA) that is based on pathology but aims at
the diagnostic workup in suspected AA is aiming at the avoid- the best possible imaging in order to discriminate preop-
ance of both delayed diagnosis with perforation, e.g., in gan- eratively between uncomplicated and complicated forms
grenous AA, as well as “negative” appendectomies. of AA. The preferred imaging modality is US rather than
AA is microscopically defined by transmural inflammation CT because of radiation protection, availability, and
of the appendix either at the tip (tip AA) or as a whole [5, 6]. costs.
The earliest changes are dilatation of the serosal vessels,
oedematous swelling of the wall followed by intramural ab-
scesses and involvement of the mesoappendix. Precursors of
Methods
AA, also known as borderline AA, show only local inflam-
mation in the lumen (intraluminal), the mucosa (mucosal) or
Search strategy
the submucosa (submucosal). Phlegmonous appendicitis is
characterised by neutrophilic infiltrates in all layers with or
Medline, Embase, and the Cochrane Library were searched
without ulceration, vascular thrombosis, and intramural ab-
for the following terms: appendicitis & clinical scores; appen-
scesses. If ischemia occurs the appendix becomes friable with
dicitis & pathology; appendicitis & ultrasound; appendicitis &
a purple, green or black discoloration in areas of necrosis
imaging; appendicitis & CT; appendicitis & classification;
(gangrenous AA). Perforation is imminent. Therefore, it is
appendicitis & guideline. Any study with these MeSH head-
classified as complicated AA. Importantly, faecoliths can be
ings published since 1970 was reviewed. Depending on the
found in approximately 30% of cases, sometimes with obvi-
level of evidence and relevance to appendicitis, classification
ous obstruction [7, 8]. Small faecoliths without obstruction
and imaging publications were included, i.e., most guidelines,
can be detected in normal appendices. The obstruction of the
systematic reviews/metaanalyses but also high quality reviews
lumen, either by a faecolith or for instance by a tumour, is an
(e.g., with regard to pathology) or randomised, as well as
important finding in the diagnostic workup [8, 9].
diagnostic trials.
Correspondingly, obstruction by a faecolith is an independent
prognostic risk factor for treatment failure in nonoperative
treatment of uncomplicated acute appendicitis [3, 10, 11]. Development of the classification of acute
In recent years, several clinical scores, based on history appendicitis (CAA)
taking, clinical examination, and laboratory tests, were devel-
oped in order to standardise clinical workup of patients with Based on the Classification of Diverticular disease by the
suspected AA. For instance, the Adult Appendicitis Score German Society of General Surgery (DGAV) and the
(AAS) with a cut-off score of 8 or less had a failure rate of German Society of Gastroenterology (DGVS) [20], as well
3.7% in women, the Appendicitis Inflammatory Response as the TNM classification by the UICC [21], a preliminary
Score (AIRS) with a cut-off score of 2 or less had a failure classification was proposed to all authors from type 0 (no
rate of 2.4% in men, and the Shera score with a cut-off score of inflammation) over uncomplicated AA (type 1) to complicat-
3 for girls and 2 for boys had a failure rate of 3.3% [12, 13]. To ed, i.e., perforated, AA (type 2). This classification was re-
this end, both the consensus statement by the EAES and the vised in four rounds using the comments of all authors.
Int J Colorectal Dis

Fig. 1 Classification of acute appendicitis (CAA) type 0 on US: Normal appendix. Shown is the transverse (a) and longitudinal (b) section of a normal
appendix with 5 layers and fully visualised

Selection of images

Both US and CT images were taken from the author’s


image databases. US images were taken with a Toshiba
Aplio 400, Canon Aplio i800, and General Electric Logiq
S8. CT images were taken with a Siemens Somatom
Sensation 64.

Classification of acute appendicitis (CAA)


based on imaging (Table 1)

Corresponding to pathology we propose CAA into five major


types:
Fig. 2 Classification of acute appendicitis (CAA) type 0 on CT: Normal
appendix. Shown is the transverse–oblique plane of the lower abdomen Type 0: normal appendix (US images in Fig. 1, CT image
showing the normal appendix (red arrow) in full length with intraluminal in Fig. 2),
oral contrast medium
Type X: appendix not visualised,
Type 1: acute uncomplicated appendicitis (US images in
Figs. 3 and 5, CT images in Figs. 4 and 6),

Fig. 3 Classification of acute appendicitis (CAA) type 1a on US: Borderline appendicitis. Shown is a the transverse and b longitundinal section of a slightly
enlarged appendix with preserved layers without periappendiceal air or fluid nor significant periappendiceal hyperechoic tissue
Int J Colorectal Dis

Table 1 Classification of acute appendicitis

Type Definition Surgical/ Gross pathology Histopathology Ultrasound findings Computed tomography
findings

uX not detectable appendix not found or not appendix not found or not
fully visualized fully visualized
0 normal normal appendix normal appendix normal appendix (< 6 mm, 3 normal appendix
layers, full length
visualized)
1 uncomplicated
1a borderline dilatated serosal vessels, intraluminal neutrophils diameter: increased to 6 to 8 diameter: increased to 6 to 8
dulling of the serosa and/or neutrophils within mm, local tenderness over mm, wall integretiy: no
the mucosa and/or the appendix, wall striation: defects luminal dilation:
submucosa and/or mucosal well preserved, luminal none, contrast
erosions dilation: none, enhancement: none
hypervascularity: none periappendiceal air or fluid:
periappendiceal air or none periappendiceal fat
significant fluid: none stranding: none
hyperechoic
periappendiceal tissue:
none
1b phlegmonous edematous swelling, neutrophils within the diameter: increased > 6 mm, dilated appendix (>6 mm),
dilatated and blood filled mucosa, submucosa, and local tenderness over the wall integretiy: no defects,
lumen, inflammation of muscularis propria, appendix, wall striation: luminal dilatation: none,
the mesoappendix extensive ulceration, intact but blurred, luminal contrast enhancement:
(exsudates) intramural microabscesses, dilation: none, present, periappendiceal
vascular thrombosis hypervascularity: present, air: none significant fluid:
periappendiceal air: none minimal periappendiceal fat
significant fluid: minimal stranding: mild ±
hyperechoic mesenteric
periappendiceal tissue: lymphadenopathy
mild, ± mesenteric
lymphadenopathy
2 complicated, not perforated
2a severe faecolith with marked marked transmural edema faecolith with distal luminal intraluminal faecolith with
phlegmonous obstruction, i.e. dis- tal and neutrophil infil- tration dilatation or extraluminal distal luminal dilatation or
with luminal dilatation, or plus obstructing faecolith, fluid, others as type 1b extraluminal fluid, others as
obstruction or adjacent fluid adjacent fluid type 1b
extraluminal
fluid
2b gangrenous friable appendix; purple, transmural inflammation with focal or complete loss of contrast enhancement defect
green or black areas of necrosis; extensive stratification, intramural air, of the appendiceal wall,
mucosal ulceration marked hyperechoic periappendiceal fat
periappendiceal tissue, stranding, intramural air
vascularity reduced
3 complicated, perforated
3a abscess or marked periappendiceal transmural neutrophil periappendiceal localised marked periappendiceal fat
appendiceal inflammation with infiltration of the appen- fluid, marked hyper- echoic stranding either confined to
mass surrounding fluid, dix and mesoappendix, periappendiceal tissue, ± the mesoappendix or
perforation, sealed with melting inflammation with abscess with localized beyond, intramural or
surrounding tissue, destructed architecture, appendiceal wall defect or directly extraluminal air ±
abscess and/or periappendiceal abscess inflamma- tory tumor; fluid, abscess and/or
inflammatory tumor covered with adjacent others as type 1b inflammatory tumor
tissue
3b free perforation friable, often incomplete or severe necrosis of the free fluid/air; appendix either free fluid/air, ascites, appendix
completely necrotic destructed appendix, invisible or in- complete, either invisible or
appendix, generalized neutrophils around the ileus, extraluminal faecolith incomplete, ileus,
peritonitis incomplete appendix, extraluminal faecolith
rarely totally destructed
Int J Colorectal Dis

Type 2: acute complicated appendicitis without perfora-


tion (US images in Figs. 7, 9, and 11, CT images in Figs.
8, 10, and 12) and
Type 3: acute complicated appendicitis with perforation
(US images Figs. 13, 15, and 17, CT images in Figs. 14,
16, and 18).

The main purpose of this classification is to discrimi-


nate complicated from uncomplicated AA based on pre-
operative US or occasionally CT. Depending on the
imaging modality employed a letter is put in front of the
number, e.g., type u2 indicating US-based or type c3 in-
dicating CT. If the appendix is removed surgically, the
classification can also be used for surgical pathology,
the intraoperative appearance, and/or the histopathology
by using the letter p, e.g., type p1. Table 1 summarises
this new classification of acute appendicitis (CAA) indi-
cating surgical pathology, histopathology, US, and finally
Fig. 4 Classification of acute appendicitis (CAA) type 1a on CT: CT findings in various types of AA.
Borderline appendicitis. Shown is the coronary plane of the right iliac First, AA can affect the inner appendiceal layers (mu-
fossa with a slightly enlarged appendix, without extraluminal air or fluid, cosa ± submucosa) leading to tenderness on US using
nor fat stranding. The appendiceal wall is intact graded compression, slightly increased diameter, pre-
served layers but no indirect signs of inflammation (AA
type 1a, i.e., borderline AA) (Fig. 3, Fig. 4). If

Fig. 5 Classification of acute appendicitis (CAA) type 1b on ultrasound: Phlegmonous appendicitis. Shown is the transverse (a,c) and longitudinal
section (b,d) of an appendix with (c,d) and without colour duplex (a,b). Layers are intact but blurred; the lumen is not dilated. Increased vascularity is
seen on colour duplex sonography. Significant periappendiceal hyperechoic tissue is shown
Int J Colorectal Dis

Fig. 7 Classification of acute appendicitis (CAA) type 2a on ultrasound:


Severe phlegmonous appendicitis with microperforation. Shown is the
longitundinal section of an enlarged appendix with a small hypoechoic
lesion (red arrows) with marked fat stranding (e.g., hyperechoic
periappendiceal tissue, yellow arrow)

Fig. 6 Classification of acute appendicitis (CAA) type 1b on CT:


Phlegmonous appendicitis. Shown is the oblique plane of the right iliac
fossa with an enlarged appendix, as well as intact appendiceal wall struc-
tures. Periappendiceal fat stranding can be seen.

Fig. 8 Classification of acute appendicitis (CAA) type 2a on CT: Severe


phlegmonous appendicitis with microperforation. Shown is the transverse
plane of the lower abdomen demonstrating an enlarged appendix (red
arrows) with an adjacent small hypodense lesion (small turquoise ar-
rows). Marked fat stranding around the appendix

Fig. 9 Classification of acute appendicitis (CAA) type 2a on ultrasound: a small faecolith (turquoise big arrow) and marked distal dilatation due to
Severe phlegmonous appendicitis with obstruction. Shown is the obstruction. The white line indicates the level of the transverse section (b)
longitundinal (a) and transverse (b) section of an enlarged appendix with as indicated by the long turquoise arrow
Int J Colorectal Dis

uncomplicated AA is more severe (type 1b, phlegmonous


AA) the appendiceal layers are blurred, the diameter is
increased (usually >8 mm), imaging shows
hypervascularity, no or minimal extraluminal fluid and
mild hyperechoic periappendiceal tissue (Fig. 5, Fig. 6).
In contrast to uncomplicated AA complicated AA is
characterised by either perforation (type 3) or either pend-
ing perforation or high likelihood of recurrence (type 2).
The latter is caused by microperforation or gangrene. The
key imaging feature is marked hyperechoic tissue on US
or marked fat stranding on CT. Marked but still localised
periappendiceal fluid (Fig. 7, Fig. 8) or obstruction (Fig.
9, Fig. 10) is seen in severe phlegmonous AA (type 2a).
Gangrenous AA (type 2b) is characterised by either intra-
mural air and/or loss of the echogenic submucosal layer
(Fig. 11, Fig. 12). Some authors have classified severe
phlegmonous AA (type 2a) and even gangrenous AA
(type 2b) as uncomplicated AA [22] supposedly because
they defined complications purely by means of the pres-
Fig. 10 Classification of acute appendicitis (CAA) type 2a on CT: Severe ence of frank perforation. Multiple studies have, however,
phlegmonous appendicitis with obstruction. Shown is the coronary plane shown that a faecolith with obstruction, marked
of a dilated appendix (red arrow) with an obstructing faecolith (turquoise
periappendiceal inflammation, and a gangrene indicate
arrow) at the base of the appendix. Mild surrounding fat stranding
imminent perforation or high likelihood of recurrence af-
ter nonoperative management [3, 7, 8, 23–26]. We, there-
fore, propose that these types should be classified as

Fig. 11 Classification of acute appendicitis (CAA) type 2b on ultrasound: The level of transverse sections of a and b,d is indicated in the longitu-
Gangrenous appendicitis. Shown is the transverse (a,b,d) and longitudi- dinal section by white lines and turquoise arrows. Strongly hyperechoic,
nal section (c) of an appendix with intact (a,c) and destroyed (c,b,d) periappendiceal tissue is marked by red arrows
layers. Decreased vascularity is seen on colour duplex sonography (d).
Int J Colorectal Dis

Fig. 12 Classification of acute appendicitis (CAA) type 2b on CT:


Gangrenous appendicitis. Shown is the sagittal plane of the right iliac
fossa with a small faecolith (yellow arrow) at the base of an enlarged Fig. 14 Classification of acute appendicitis (CAA) type 3a on CT (local-
appendix (red arrow) with blurred margins, intramural air (turquoise ar- ised, perforated AA): Appendicitis with sealed perforation. Shown is a
row) and marked periappendiceal fat stranding (black arrow) coronary plane of the abdomen with a slightly enlarged appendix (red
arrow) and a large extraluminal hypodense lesion indicating a sealed
abscess (>2 cm, red arrow) with surrounding fat stranding

Fig. 13 Classification of acute appendicitis (CAA) type 3a on ultrasound defect of the appendiceal wall (b, yellow arrow) and extraluminal
(localised, perforated AA): Appendicitis with sealed perforation. Shown hypoechoic lesion indicating a sealed abscess (>2 cm, red arrow) with
is the proximal transverse (a) and distal transverse (b, white arrow) sec- surrounding hyperechoic tissue
tion of an enlarged appendix with a faecolith (turquoise arrow), localised
Int J Colorectal Dis

Fig. 15 Classification of acute appendicitis (CAA) type 3a on ultrasound inhomogenous, inflammatory tumour, as well as the surrounding
(localised, perforated AA): Appendicitis with appendiceal mass. Shown hyperechoic tissue. Colour duplex sonography shows vascular structures
is the longitudinal section of an enlarged appendix with an inside the “tumour”

Fig. 16 Classification of acute appendicitis (CAA) type 3a on CT (local- Fig. 17 Classification of acute appendicitis (CAA) type 3b on ultrasound:
ised, perforated AA): Appendicitis with appendiceal mass. Shown is a Appendicitis with free perforation. Shown is the right iliac fossa with
transverse plane of the abdomen with a slightly enlarged appendix with a hypoechoic, inhomogeneous fluid and echogenic dots (air bubbles) indi-
perforation (red arrow) and an adjacent inhomogenous, hypodense, and cating free perforation due to a necrotic, destroyed, and therefore unde-
inflammatory tumour (turquoise arrow), as well as the surrounding fat tectable appendix
stranding

complicated AA in accordance with the consensus state-


ment by the EAES [4].
If perforation is detected this can present as sealed perfora-
tion (type 3a, Fig. 13 and Fig. 14) with an abscess or as free
perforation with free fluid, air, and pus in the abdominal cavity
(type 3b, Fig. 17 and Fig. 18). Occasionally, an appendiceal
mass involving surrounding small or large bowel loops can be
found which is also a more localised form of perforation, i.e.,
type 3a (Fig. 15 and Fig. 16) [27]. A more detailed description
of the surgical pathology, histology, US, and CT findings can
be found in Table 1.

Fig. 18 Classification of acute appendicitis (CAA) type 3b on CT:


Appendicitis with free perforation. Shown is a transverse plane of the Diagnostic and therapeutic algorithm
lower abdomen with free fluid, air and marked fat stranding indicating for suspected AA based on CAA
free perforation due to a necrotic, destroyed, and therefore undetectable
appendix State of the art AA management requires not only the cor-
rect diagnosis but also the distinction between complicated
Int J Colorectal Dis

Table 2 Standardised ultrasound reporting for suspected appendicitis

Category Parameter Subgroup Detailed description

General Location [pelvic; subcecal; retroileal; retrocecal; ectopic; preileal]


Visualisation [complete; incomplete; not visualised]
Local tenderness [yes; no; unclear]
Appendix Compressibility [yes; no]
Total diameter [in mm]
Lumen diameter [in mm]
air (hyperechoic dot) [present; absent]
faecolith (echogenic) [none; present, no distal dilatation; present with distal dilatation]
Wall diameter [in mm]
layers [preserved stratification; blurred stratification; localised loss of stratification; generalised
loss of stratification]
vascularity [normal; increased within the appendix; locally reduced; reduced in the whole appendix]
perforation [none; localised/small; complete/large]
intramural air [present; absent]
(hyperechoic dot)
Surrounding Periappendiceal fat [normal; slightly increased hyperechoic tissue; markedly increased hyperechoic tissue]
Mesenteric lymph nodes [not visible; visible, normal; visible, enlarged, reactive; visible, enlarged, likely neoplastic]
Fluid (hypoechoic or [minute periappendiceal (< 5 mm); little periappendiceal (5-20 mm); large, localised (> 2
echofree) cm); free ascites]
Air (hyperechoic dot, [outside the wall; within a localised fluid collection (abscess); within free fluid (free
extramural) perforation)]
Special features Inflammatory [present; absent]
tumour/mass
Ileal blowel loops [normal; dilated, no peristalsis; dilated, increased peristalsis]
Caecal tumor [present; absent]
Others [present; absent]

Summary: e.g. acute appendicitis type u1b according to CAA (phlegmonous appendicitis without obstruction)

Table 3 Standardised computed tomography reporting for suspected appendicitis

Category Parameter Subgroup Detailed description

General Location [pelvic; subcecal; retroileal; retrocecal; ectopic; preileal]


Visualisation [complete; incomplete; not visualised]
Local tenderness [yes; no; unclear]
Appendix Total diameter [in mm]
Lumen diameter [in mm]
air (black dot) [present; absent]
faecolith (bright) [none; present, no distal dilatation; present with distal dilatation]
Wall diameter [in mm]
vascularity [normal; enhanced contrast; locally reduced; overall reduced]
perforation [none; localised/small; complete/large]
intramural air (hyperechoic [present; absent]
dot)
Surrounding Periappendiceal fat [normal; slight fat stranding; marked fat stranding]
Mesenteric lymph [not visible; visible, normal; visible, enlarged, reactive; visible, enlarged, likely neoplastic]
nodes
Fluid (dark grey) [minute periappendiceal (< 5 mm); little periappendiceal (5-20 mm); large, localised (> 2 cm);
free ascites]
Air (black) [outside the wall; within a localised fluid collection (abscess); within free fluid (free
perforation)]
Special features Inflammatory tumour/mass [present; absent]
Ileal blowel loops [normal; dilated, no peristalsis; dilated, increased peristalsis]
Caecal tumor [present; absent]
Others [present; absent]

Summary: e.g. acute appendicitis type 1b according to CAA (phlegmonous appendicitis without obstruction)
Int J Colorectal Dis

Fig. 19 Diagnostic algorithm for patients with suspected acute appendicitis (AA). *According to clinical score, laboratory and US; # HR, high risk; IR,
intermediate risk; LR, low risk; US, ultrasound; CT, computer tomography

and uncomplicated forms of AA. Therefore, history taking, be emphasised that visualisation of the complete appendix
clinical examination and emergency laboratory analysis including the tip is very important. If the appendix cannot
must be supplemented with abdominal US including so- be fully visualised both clinical scores and the patient’s age
phisticated visualisation of the appendix. The US tech- can help to make a decision how to proceed. If the situation
nique has been described elsewhere with visualisation in remains unclear, diagnostic laparoscopy is also a good op-
up to 95% of cases and sensitivities of up to 99% [16, 19, tion to proceed although one randomised trial did not show
28–31]. Particularly, the anatomical variations need to be a benefit when comparing laparoscopy to active clinical
considered in order to keep the proportion of nonvisualised observation [44–46].
appendices as low as possible [32, 33]. In order to accom- Figure 19 summarises the recommended diagnostic
plish the best possible imaging results, it has been shown workup in suspected AA leading either to discharge from
that standardised reporting leads to better diagnostic results the emergency room or further treatment based on the new
for both US and CT [34–38]. Therefore, Table 2 shows a Classification of AA (see Fig. 20). Once AA is diagnosed
standardised reporting scheme for US of the appendix and the new CAA allows differentiating between uncomplicat-
Table 3 for CT scans. If a CT scan is used it is recommend- ed and complicated forms of AA. Free perforation (type
ed to limit the range and the dose in order to reduce radi- 3b) and gangrenous AA (type 2b) require an emergency
ation [35, 39, 40]. The not completely visualised appendix operation. Highly inflamed, phlegmonous AA, as well as
can either be reexamined by US later (particularly in low phlegmonous AA with obstruction (both type 2a), is un-
risk or young intermediate risk patients) or can be evaluat- likely to be cured upon sole antibiotic treatment and is,
ed further by CT, particularly in high-risk patients and therefore, no candidate for nonoperative management [3,
patients over 40 years of age. Importantly, delaying sur- 7, 8, 23, 25, 26]. Patients with abscesses/sealed perforation
gery because of nonvisualisation of the appendix does not or an appendiceal mass (both type 3a) can be treated by
lead to increased perforation rates when looking at all pa- US- or CT-guided drainage and/or antibiotics depending
tients with AA, even if they are pregnant [41–43]. It must on their size, usually followed by elective surgery later on
Int J Colorectal Dis

Fig. 20 Therapeutic algorithm for patients with confirmed acute appendicitis (AA). * microperforation; # HR, high risk; IR, intermediate risk; LR, low
risk; Sx, surgery; PAA, phlegmonous AA; US, ultrasound; CT, computer tomography; u, based on US; c, based on CT; AB, antibiotics; h, hours

[1]. Some data even suggest that appendiceal masses References


might not even need later surgery at all [27]. Finally, un-
complicated AA can either be treated nonoperatively, e.g., 1. Di Saverio S, Podda M, De Simone B, Ceresoli M, Augustin G,
Gori A, Boermeester M, Sartelli M, Coccolini F, Tarasconi A,
in borderline cases possibly even without antibiotics but
De’Angelis N, Weber DG, Tolonen M, Birindelli A, Biffl W,
with US and clinical follow-up [47] or, possibly, in mild Moore EE, Kelly M, Soreide K, Kashuk J, Ten Broek R, Gomes
forms of phlegmonous AA provided there is no high risk CA, Sugrue M, Davies RJ, Damaskos D, Leppaniemi A,
situation [2, 3]. Whilst no data is available about the re- Kirkpatrick A, Peitzman AB, Fraga GP, Maier RV, Coimbra R,
Chiarugi M, Sganga G, Pisanu A, De’Angelis GL, Tan E, Van
currence rate of borderline AA upon nonoperative treat-
Goor H, Pata F, Di Carlo I, Chiara O, Litvin A, Campanile FC,
ment the recurrence of uncomplicated AA (type 1b) was Sakakushev B, Tomadze G, Demetrashvili Z, Latifi R, Abu-Zidan
39.1% of patients within 5 years in well characterised pa- F, Romeo O, Segovia-Lohse H, Baiocchi G, Costa D, Rizoli S,
tients [48]. Since the postoperative complication rate of Balogh ZJ, Bendinelli C, Scalea T, Ivatury R, Velmahos G,
Andersson R, Kluger Y, Ansaloni L, Catena F (2020) Diagnosis
appendectomy is low when looking at patients with un-
and treatment of acute appendicitis: 2020 update of the WSES
complicated AA (type 1b) the threshold to operate should Jerusalem guidelines. World J Emerg Surg 15(1):27. https://doi.
be rather low unless significant comorbidity is present org/10.1186/s13017-020-00306-3
[49]. Still, a population-based study from Ontario showed 2. Podda M, Gerardi C, Cillara N, Fearnhead N, Gomes CA, Birindelli
up to 25.2% postoperative complications (including read- A, Mulliri A, Davies RJ, Di Saverio S (2019) Antibiotic treatment
and appendectomy for uncomplicated acute appendicitis in adults
mission, emergency room visits, and prolonged hospital and children: a systematic review and meta-analysis. Ann Surg
stays) [50]. When looking at patients with nonperforated 270(6):1028–1040. https://doi.org/10.1097/SLA.
forms of AA without obstruction a recent randomised trial 0000000000003225
detected AA recurrence in still 25% of patients within 90 3. Collaborative C, Flum DR, Davidson GH, Monsell SE, Shapiro NI,
Odom SR, Sanchez SE, Drake FT, Fischkoff K, Johnson J, Patton
days [3]. However, severe phlegmonous types of appendi- JH, Evans H, Cuschieri J, Sabbatini AK, Faine BA, Skeete DA,
citis (type 2a), as well as gangrenous types of AA (type Liang MK, Sohn V, McGrane K, Kutcher ME, Chung B, Carter
2b), were counted as uncomplicated AA in this study. DW, Ayoung-Chee P, Chiang W, Rushing A, Steinberg S, Foster
Importantly, just 3.5% had an “US only” diagnostic ap- CS, Schaetzel SM, Price TP, Mandell KA, Ferrigno L, Salzberg M,
DeUgarte DA, Kaji AH, Moran GJ, Saltzman D, Alam HB, Park
proach compared to 79.6% a “CT only” reflecting possible PK, Kao LS, Thompson CM, Self WH, Yu JT, Wiebusch A,
improvements with regard to radiation protection. Winchell RJ, Clark S, Krishnadasan A, Fannon E, Lavallee DC,
Comstock BA, Bizzell B, Heagerty PJ, Kessler LG, Talan DA
(2020) A randomized trial comparing antibiotics with appendecto-
Acknowledgement We thank M. Knörzer for secretarial assistance and my for appendicitis. N Engl J Med 383(20):1907–1919. https://doi.
A. De Forrest, MD, and M.W. Hoffmann, MD PhD, for critical reading of org/10.1056/NEJMoa2014320
the manuscript. 4. Gorter RR, Eker HH, Gorter-Stam MA, Abis GS, Acharya A,
Ankersmit M, Antoniou SA, Arolfo S, Babic B, Boni L, Bruntink
Int J Colorectal Dis

M, van Dam DA, Defoort B, Deijen CL, DeLacy FB, Go PM, 19. Dirks K, Calabrese E, Dietrich CF, Gilja OH, Hausken T,
Harmsen AM, van den Helder RS, Iordache F, Ket JC, Muysoms Higginson A, Hollerweger A, Maconi G, Maaser C, Nuernberg
FE, Ozmen MM, Papoulas M, Rhodes M, Straatman J, Tenhagen D, Nylund K, Pallotta N, Ripolles T, Romanini L, Saftoiu A,
M, Turrado V, Vereczkei A, Vilallonga R, Deelder JD, Bonjer J Serra C, Wustner M, Sporea I (2019) EFSUMB position paper:
(2016) Diagnosis and management of acute appendicitis. EAES recommendations for gastrointestinal ultrasound (GIUS) in acute
consensus development conference 2015. Surg Endosc 30(11): appendicitis and diverticulitis. Ultraschall Med 40(2):163–175.
4668–4690. https://doi.org/10.1007/s00464-016-5245-7 https://doi.org/10.1055/a-0824-6952
5. Carr NJ (2000) The pathology of acute appendicitis. Ann Diagn 20. Kruis W, Germer CT, Leifeld L, German Society for
Pathol 4(1):46–58. https://doi.org/10.1016/s1092-9134(00)90011-x Gastroenterology D, Metabolic D, The German Society for G,
6. Mazeh H, Epelboym I, Reinherz J, Greenstein AJ, Divino CM Visceral S (2014) Diverticular disease: guidelines of the german
(2009) Tip appendicitis: clinical implications and management. society for gastroenterology, digestive and metabolic diseases and
Am J Surg 197(2):211–215. https://doi.org/10.1016/j.amjsurg. the german society for general and visceral surgery. Digestion
2008.04.016 90(3):190–207. https://doi.org/10.1159/000367625
7. Alaedeen DI, Cook M, Chwals WJ (2008) Appendiceal fecalith is 21. Brierley JD, Gospodarowicz MK, Wittekind C (2017) TNM clas-
associated with early perforation in pediatric patients. J Pediatr Surg sification of malignant tumours. 8th edition edn Oxford
43(5):889–892. https://doi.org/10.1016/j.jpedsurg.2007.12.034 22. Gonzalez DO, Lawrence AE, Cooper JN, Sola R Jr, Garvey E,
8. Mallinen J, Vaarala S, Makinen M, Lietzen E, Gronroos J, Ohtonen Weber BC, St Peter SD, Ostlie DJ, Kohler JE, Leys CM, Deans
P, Rautio T, Salminen P (2019) Appendicolith appendicitis is clin- KJ, Minneci PC (2018) Can ultrasound reliably identify complicat-
ically complicated acute appendicitis-is it histopathologically dif- ed appendicitis in children? J Surg Res 229:76–81. https://doi.org/
ferent from uncomplicated acute appendicitis. Int J Color Dis 34(8): 10.1016/j.jss.2018.03.012
1393–1400. https://doi.org/10.1007/s00384-019-03332-z 23. Blumfield E, Nayak G, Srinivasan R, Muranaka MT, Blitman NM,
9. Gaetke-Udager K, Maturen KE, Hammer SG (2014) Beyond acute Blumfield A, Levin TL (2013) Ultrasound for differentiation be-
appendicitis: imaging and pathologic spectrum of appendiceal pa- tween perforated and nonperforated appendicitis in pediatric pa-
thology. Emerg Radiol 21(5):535–542. https://doi.org/10.1007/ tients. AJR Am J Roentgenol 200(5):957–962. https://doi.org/10.
s10140-013-1188-7 2214/AJR.12.9801
24. Ishiyama M, Yanase F, Taketa T, Makidono A, Suzuki K, Omata F,
10. Mahida JB, Lodwick DL, Nacion KM, Sulkowski JP, Leonhart KL,
Saida Y (2013) Significance of size and location of appendicoliths
Cooper JN, Ambeba EJ, Deans KJ, Minneci PC (2016) High failure
as exacerbating factor of acute appendicitis. Emerg Radiol 20(2):
rate of nonoperative management of acute appendicitis with an
125–130. https://doi.org/10.1007/s10140-012-1093-5
appendicolith in children. J Pediatr Surg 51(6):908–911. https://
25. Kuhn KJ, Brooke Jeffrey R, Olcott EW (2019) Luminal obstruction
doi.org/10.1016/j.jpedsurg.2016.02.056
in uncomplicated appendicitis: detection with sonography and po-
11. Shindoh J, Niwa H, Kawai K, Ohata K, Ishihara Y, Takabayashi N,
tential clinical implications. J Clin Ultrasound 47(3):113–119.
Kobayashi R, Hiramatsu T (2010) Predictive factors for negative
https://doi.org/10.1002/jcu.22655
outcomes in initial non-operative management of suspected appen-
26. Rawolle T, Reismann M, Minderjahn MI, Bassir C, Hauptmann K,
dicitis. J Gastrointest Surg 14(2):309–314. https://doi.org/10.1007/
Rothe K, Reismann J (2019) Sonographic differentiation of com-
s11605-009-1094-1
plicated from uncomplicated appendicitis. Br J Radiol 92(1099):
12. Bhangu A, Collaborative RSGobotWMR (2020) Evaluation of ap-
20190102. https://doi.org/10.1259/bjr.20190102
pendicitis risk prediction models in adults with suspected appendi-
27. Forsyth J, Lasithiotakis K, Peter M (2017) The evolving manage-
citis. Br J Surg 107(1):73–86. https://doi.org/10.1002/bjs.11440
ment of the appendix mass in the era of laparoscopy and interven-
13. Collaborative RSGobotWMR (2020) Appendicitis risk prediction tional radiology. Surgeon 15(2):109–115. https://doi.org/10.1016/j.
models in children presenting with right iliac fossa pain (RIFT surge.2016.08.002
study): a prospective, multicentre validation study. Lancet Child 28. Chang ST, Jeffrey RB, Olcott EW (2014) Three-step sequential
Adolesc Health 4(4):271–280. https://doi.org/10.1016/S2352- positioning algorithm during sonographic evaluation for appendici-
4642(20)30006-7 tis increases appendiceal visualization rate and reduces CT use.
14. Drake FT, Florence MG, Johnson MG, Jurkovich GJ, Kwon S, AJR Am J Roentgenol 203(5):1006–1012. https://doi.org/10.
Schmidt Z, Thirlby RC, Flum DR, Collaborative S (2012) 2214/AJR.13.12334
Progress in the diagnosis of appendicitis: a report from 29. Lee JH, Jeong YK, Hwang JC, Ham SY, Yang SO (2002) Graded
Washington State’s Surgical Care and Outcomes Assessment compression sonography with adjuvant use of a posterior manual
Program. Ann Surg 256(4):586–594. https://doi.org/10.1097/SLA. compression technique in the sonographic diagnosis of acute ap-
0b013e31826a9602 pendicitis. AJR Am J Roentgenol 178(4):863–868. https://doi.org/
15. Lietzen E, Mallinen J, Gronroos JM, Rautio T, Paajanen H, 10.2214/ajr.178.4.1780863
Nordstrom P, Aarnio M, Rantanen T, Sand J, Mecklin JP, Jartti 30. Lee JH, Jeong YK, Park KB, Park JK, Jeong AK, Hwang JC (2005)
A, Virtanen J, Ohtonen P, Salminen P (2016) Is preoperative dis- Operator-dependent techniques for graded compression sonogra-
tinction between complicated and uncomplicated acute appendicitis phy to detect the appendix and diagnose acute appendicitis. AJR
feasible without imaging? Surgery 160(3):789–795. https://doi.org/ Am J Roentgenol 184(1):91–97. https://doi.org/10.2214/ajr.184.1.
10.1016/j.surg.2016.04.021 01840091
16. Hollerweger A (2006) Acute appendicitis: sonographic evaluation. 31. Puylaert JB (1986) Acute appendicitis: US evaluation using graded
Ultraschall Med 27(5):412–426; quiz 427-432. https://doi.org/10. compression. Radiology 158(2):355–360. https://doi.org/10.1148/
1055/s-2006-927118-2 radiology.158.2.2934762
17. Bakker OJ, Go PM, Puylaert JB, Kazemier G, Heij HA, Werkgroep 32. Kacprzyk A, Dro SJ, Stefura T, Krzysztofik M, Jasinska K,
richtlijn Diagnostiek en behandeling van acute a (2010) Guideline Pedziwiatr M, Major P, Holda MK (2020) Variations and morpho-
on diagnosis and treatment of acute appendicitis: imaging prior to metric features of the vermiform appendix: a systematic review and
appendectomy is recommended. Ned Tijdschr Geneeskd 154:A303 meta-analysis of 114,080 subjects with clinical implications. Clin
18. Hoffmann M, Anthuber M (2019) Rational diagnostics of acute Anat 33(1):85–98. https://doi.org/10.1002/ca.23474
appendicitis. Chirurg 90(3):173–177. https://doi.org/10.1007/ 33. Lin W, Jeffrey RB, Trinh A, Olcott EW (2017) Anatomic reasons for
s00104-018-0755-6 failure to visualize the appendix with graded compression
Int J Colorectal Dis

sonography: insights from contemporaneous CT. AJR Am J 43. Tankel J, Yellinek S, Shechter Y, Greenman D, Ioscovich A, Grisaru-
Roentgenol 209(3):W128–W138. https://doi.org/10.2214/AJR.17. Granovsky S, Reissman P (2019) Delaying laparoscopic surgery in
18059 pregnant patients with an equivocal acute appendicitis: a step-wise
34. Fallon SC, Orth RC, Guillerman RP, Munden MM, Zhang W, approach does not affect maternal or fetal safety. Surg Endosc 33(9):
Elder SC, Cruz AT, Brandt ML, Lopez ME, Bisset GS (2015) 2960–2966. https://doi.org/10.1007/s00464-018-6600-7
Development and validation of an ultrasound scoring system for 44. Decadt B, Sussman L, Lewis MP, Secker A, Cohen L, Rogers C,
children with suspected acute appendicitis. Pediatr Radiol 45(13): Patel A, Rhodes M (1999) Randomized clinical trial of early lapa-
1945–1952. https://doi.org/10.1007/s00247-015-3443-4 roscopy in the management of acute non-specific abdominal pain.
35. Kim HY, Park JH, Lee YJ, Lee SS, Jeon JJ, Lee KH (2018) Br J Surg 86(11):1383–1386. https://doi.org/10.1046/j.1365-2168.
Systematic review and meta-analysis of CT features for differenti- 1999.01239.x
ating complicated and uncomplicated appendicitis. Radiology 45. Kraemer M, Ohmann C, Leppert R, Yang Q (2000) Macroscopic
287(1):104–115. https://doi.org/10.1148/radiol.2017171260 assessment of the appendix at diagnostic laparoscopy is reliable.
36. Larson DB, Trout AT, Fierke SR, Towbin AJ (2015) Improvement in Surg Endosc 14(7):625–633. https://doi.org/10.1007/
diagnostic accuracy of ultrasound of the pediatric appendix through s004640000122
the use of equivocal interpretive categories. AJR Am J Roentgenol 46. Morino M, Pellegrino L, Castagna E, Farinella E, Mao P (2006)
204(4):849–856. https://doi.org/10.2214/AJR.14.13026 Acute nonspecific abdominal pain: a randomized, controlled trial
37. Nielsen JW, Boomer L, Kurtovic K, Lee E, Kupzyk K, Mallory R, comparing early laparoscopy versus clinical observation. Ann Surg
Adler B, Bates DG, Kenney B (2015) Reducing computed tomog- 244(6):881–886; discussion 886-888. https://doi.org/10.1097/01.
raphy scans for appendicitis by introduction of a standardized and sla.0000246886.80424.ad
validated ultrasonography report template. J Pediatr Surg 50(1): 47. Park HC, Kim MJ, Lee BH (2017) Randomized clinical trial of
144–148. https://doi.org/10.1016/j.jpedsurg.2014.10.033 antibiotic therapy for uncomplicated appendicitis. Br J Surg
38. Nordin AB, Sales S, Nielsen JW, Adler B, Bates DG, Kenney B 104(13):1785–1790. https://doi.org/10.1002/bjs.10660
(2018) Standardized ultrasound templates for diagnosing appendi-
48. Salminen P, Tuominen R, Paajanen H, Rautio T, Nordstrom P,
citis reduce annual imaging costs. J Surg Res 221:77–83. https://
Aarnio M, Rantanen T, Hurme S, Mecklin JP, Sand J, Virtanen J,
doi.org/10.1016/j.jss.2017.07.002
Jartti A, Gronroos JM (2018) Five-year follow-up of antibiotic
39. Corwin MT, Chang M, Fananapazir G, Seibert A, Lamba R (2015)
therapy for uncomplicated acute appendicitis in the APPAC ran-
Accuracy and radiation dose reduction of a limited abdominopelvic
domized clinical trial. JAMA 320(12):1259–1265. https://doi.org/
CT in the diagnosis of acute appendicitis. Abdom Imaging 40(5):
10.1001/jama.2018.13201
1177–1182. https://doi.org/10.1007/s00261-014-0280-0
40. Park JH, Jeon JJ, Lee SS, Dhanantwari AC, Sim JY, Kim HY, Lee 49. Stoss C, Nitsche U, Neumann PA, Kehl V, Wilhelm D, Busse R,
KH (2018) Can We Perform CT of the Appendix with Less Than 1 Friess H, Nimptsch U (2021) Acute appendicitis: trends in surgical
mSv? A de-escalating dose-simulation study. Eur Radiol 28(5): treatment—a population-based study of over 800 000 patients.
1826–1834. https://doi.org/10.1007/s00330-017-5159-3 Dtsch Arztebl Int 118 (Forthcoming) https://doi.org/10.3238/
41. Sauvain MO, Slankamenac K, Muller MK, Wildi S, Metzger U, arztebl.m2021.0118
Schmid W, Wydler J, Clavien PA, Hahnloser D (2016) Delaying 50. Patel SV, SJM GPA, Lajkosz K, Nanji S, Brogly SB (2018) Timing
surgery to perform CT scans for suspected appendicitis decreases of surgery and the risk of complications in patients with acute ap-
the rate of negative appendectomies without increasing the rate of pendicitis: a population-level case-crossover study. J Trauma Acute
perforation nor postoperative complications. Langenbeck's Arch Care Surg 85(2):341–347. https://doi.org/10.1097/TA.
Surg 401(5):643–649. https://doi.org/10.1007/s00423-016-1444-x 0000000000001962
42. Stewart JK, Olcott EW, Jeffrey RB (2012) Sonography for appendici-
tis: nonvisualization of the appendix is an indication for active clinical Publisher’s note Springer Nature remains neutral with regard to jurisdic-
observation rather than direct referral for computed tomography. J Clin tional claims in published maps and institutional affiliations.
Ultrasound 40(8):455–461. https://doi.org/10.1002/jcu.21928

You might also like