Introduction
As the most common cause of sudden abdominal pain requiring surgery, acute appendicitis is frequently seen in emergency departments. According to collected data from the USA, the overall lifetime risk of acute appendicitis is approximately 8% [1]. Thus, appendectomies are among the abdominal procedures most frequently performed by general surgeons. Since the first successful laparoscopic appendectomy (LA) was performed in 1983 [2], this minimally invasive approach has gradually become the preferred operative technique for acute appendicitis [3]. Laparoscopic appendectomy in comparison to open appendectomies presented major advantages: a lower incidence of postoperative wound infections, pain reduction, and shorter length of hospital stay (LOS) [4–6]. Moreover, LAs are associated with an earlier return to normal activity [1]. The drawback of minimally invasive access is an increased incidence of intraabdominal abscess (IAA) formation after LA [1]. It is associated with higher morbidity and increased LOS. The majority of patients who develop IAA require therapeutic intervention, starting with conservative antibiotic treatment, percutaneous drainage, or reoperation. Previous studies have shown some risk factors of developing IAA; however, the limited data on the risk of IAA specifically after laparoscopic procedures call for further analysis. Moreover, the identification of risk factors for IAA formation may allow doctors to select patients prone to this complication and take preventative measures. Based on a large cohort of patients, we aimed to establish both the incidence and the possible risk factors for the development of IAA after LA for appendicitis. Additionally, we evaluated the influence of IAA formation on patients’ postoperative outcomes.
Aim
This study aims to identify potential risk factors for IAA after LA and determine LA influence on postoperative outcomes.
Material and methods
This multicenter study was performed across 18 surgical centers in both Poland and Germany over a 6-month period. The data collected from patients admitted for laparoscopic appendectomy were assembled in an internet-based database. The design and implementation of this study followed the guidelines of the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement [7]. This study includes both retrospective data from previous patients at each center and data from patients enrolled during the study period. Data acquisition was performed by the coordinating surgeon and the local team of nurses, anesthesiologists, and assistants. The database recorded the following variables from each center: annual number of laparoscopic appendectomies performed, patient characteristics (sex, age, body mass index (BMI), ASA score, history of smoking, diabetes mellitus, timing from onset of symptoms to surgery, Alvarado score), white blood cell count (WBC), C-reactive protein level (CRP), operative parameters (operative time, type of surgeon performing the appendectomy (resident/specialist), type of AA (uncomplicated/complicated), intraoperative adverse events, and postoperative outcomes (postoperative morbidity, need for surgical reintervention, LOS, need for readmission).
The study and control groups were divided based on the presence of IAA development in the postoperative period. Complicated AA was diagnosed based on imaging diagnostics and/or visualization during relaparoscopy/relaparotomy performed due to the patient’s condition.
This study did not implement any changes in patient treatment. A primary investigator monitored this study. He processed and verified any missing or unclear data submitted to the database. The data collected were anonymized and had no identifying patient information. The only hospital data included were the number of laparoscopic appendectomies performed annually. The study did not need informed consent or formal approval by a local ethics committee due to the observational nature. The project was supported by the Polish Videosurgery Society – a chapter of the Association of Polish Surgeons.
Statistical analysis
Statistical analyses were done using StatSoft Statistica 13.0 PL (StatSoft Inc., Tulsa, Oklahoma, USA). Continuous variables were presented using means with standard deviations (SD) or medians with inter-quartile ranges (IQR) for skewed variables. Then, comparisons between groups were done using Student’s t test for normally distributed variables and the Mann-Whitney test for skewed variables. Dichotomous variables were included in χ2 Pearson’s, Yates’ and Fisher’s exact tests, depending on the quantities in the subgroups. Finally, univariate and multivariate logistic regression models were built to determine risk factors for postoperative complications. Results were considered statistically significant when p-values were < 0.05. In the case of missing data, pairwise deletion was used.
Results
This study includes data from 4618 patients. Characteristics of the study group are presented in Table I. The majority of patients (3269/4618 70.79%) underwent LAs in centers performing over 50 LAs per year. 2034 (44.05%) patients were operated on by surgical residents under the supervision of an attending surgeon. 2409 (52.2%) patients were male and 2209 (47.8%) were female. Median age of the entire study group was 33 years (IQR: 24–47). Median BMI was 24.8 kg/m2 (IQR: 22.03–28.5). 794 (19.19%) patients were active smokers and 147 (3.18%) had diabetes mellitus. Concerning the ASA physical status classification system, 3214 (69.60%) patients were classified as ASA class I, 1213 (26.27%) ASA class II, 184 (3.98%) ASA class III, and 7 (0.15%) ASA class IV. 1463 (31.68%) patients complained of symptoms of AA > 48 h before surgery. Median WBC was 13.1 × 1000 per mm3 (IQR: 10.04–16.1) and CRP was 27.3 mg/l (6.2–72).
Table I
Fifty-one (1.10%) patients developed IAA in the postoperative period. Groups differed in almost all analyzed parameters. Full preoperative characteristics of these two groups are presented in Table I.
Operative parameters for both groups are presented in Table II. Median operative time was longer in the IAA group (70 vs. 54 min, p = 0.001). Patients with eventual IAA formation had a higher incidence of complicated appendicitis (36/51 (71%) vs. 1233/3334 (27%), p < 0.001). Intraoperative periappendiceal abscesses were found in 24 (47.05%) patients in the IAA group and in 534 (11.7%) patients in the non-IAA group (p < 0.001). Intraoperative adverse events occurred in 5 (9.8%) patients in the IAA group and in 99 (2.17%) patients in the non-IAA group (p = 0.001). Drains were left in the peritoneal cavity in 48 (94%) patients in the IAA group and in 3444 (75.41%) patients in the non-IAA group (p = 0.004).
Table II
Overall, 33 (64.71%) patients with IAA and 65 (1.42%) without an IAA required reintervention after the primary procedure (p < 0.001). Out of them 3 (5.88%) patients underwent percutaneous drainage of the abscess and 30 (58.82%) required another surgery. Of the cases necessitating other surgical interventions, 14 (27.45%) had a relaparotomy, 11 (21.56%) had a relaparoscopy with 1 case of conversion, and in 5 (9.80%) cases there was no information whether reintervention was open or laparoscopic. Eighteen (35.29%) patients were treated conservatively with antibiotics.
Median LOS was longer in the IAA group (9 (IQR: 4–13) vs. 3 (IQR: 2–4) days, p = 0.001). Thirty-three (64.71%) patients in the IAA group and 194 (14.48%) patients in the non-IAA group needed to spend longer than 8 days (longer than 2* third quartile) in the hospital. Patients with IAA were readmitted more frequently compared to those with no abscess formation (21 (41%) vs. 89 (2.08%), p < 0.001).
The results of the univariate analysis of IAA risk factors utilizing pre- and perioperative parameters are shown in Table III. The following parameters were associated with the formation of IAA: male sex (OR = 2.02, 95% CI: 1.11–3.66), age > 35 years (OR = 1.93, 95% CI: 1.10–3.37), diabetes mellitus (OR = 3.46, 95% CI: 1.35–8.87), time from onset of symptoms to LA > 48 h (OR = 2.47, 95% CI: 1.40–4.34), Alvarado scale (OR = 1.15, 95% CI: 1.01–1.31 with every point higher), CRP > 50 mg/l (OR = 3.96, 95% CI: 2.09–7.49), complicated appendicitis, i.e. perforated/gangrenous or with periappendiceal abscess (OR = 6.49, 95% CI: 3.54–11.90), gangrenous appendicitis (OR = 2.48, 95% CI: 1.61–5.00), perforated/autoamputated appendix (OR = 7.63, 95% CI: 4.00–14.56) intraoperative adverse events (OR = 4.89, 95% CI: 1.90–12.58). In turn, purulent appendicitis was found to lower the risk of IAA (OR = 0.25, 95% CI: 0.14–0.44).
Table III
In the multivariate model, only the presence of complicated appendicitis (OR = 2.98, 95% CI: 1.11–8.04) was statistically significant.
Further analysis showed that the presence of IAA has a significant influence on postoperative reintervention (OR = 126.95, 95% CI: 67.98–237.06), prolonged length of stay > 8 days (OR = 41.32, 95% CI: 22.86–74.72) and readmission rate (OR = 33.89, 95% CI: 18.60–34.73) (Table IV).
Discussion
Based on this large volume observational study, we concluded that the development of an IAA is strongly associated with the underlying state of the appendicitis. The presence of complicated AA remained the only independent risk factor for postoperative IAA formation. We also confirmed that once IAA is diagnosed, it strongly affects postoperative outcomes, such as increased surgical reintervention rate, prolonged LOS, and higher readmission rate.
Laparoscopic appendectomy is the most commonly used surgical intervention for AA, with more than 50% of cases being treated in this manner in developed countries [8–10]. Nevertheless, recent meta-analyses, including the most recent 2010 Cochrane systematic review, revealed a higher incidence of postoperative IAA formation after LA in comparison to OA [1]. This review was the second update of an original 2002 publication [11]. Interestingly, each update of this original publication attempts to decrease the varying rates of IAA formation between LA and OAs; the likelihood of IAA after LA was nearly threefold after an LA (OR = 2.77) in the original publication, then decreased in the first update in 2004 (OR = 2.48), and further decreased in the second update in 2010 (OR = 1.87) [1, 11, 12]. Additionally, in the recent 2016 cumulative meta-analysis, a change in treatment results was noted – the effect size in favor of open procedures began to disappear after 2001, leading to an insignificant result with an overall cumulative OR of 1.32 (95% CI: 0.84–2.10) when laparoscopic appendectomy was compared with open appendectomy [13]. This is in line with several other meta-analyses [14–16].
This study allowed us to confirm that IAA is, in fact, a rare complication. The rate of IAA formation in our cohort was 1.1%, which, while low, is still in the range reported elsewhere [17–19]. Nevertheless, since it theoretically can occur in every patient undergoing an appendectomy, the identification of potential risk factors might be helpful in postoperative follow-up of patients.
In this study group, the univariate logistic regression models revealed several risk factors for postoperative IAA: male sex, age greater than 35 years, diabetes mellitus, longer duration of symptoms, higher Alvarado score, higher WBC and CRP levels, longer operative time, intraoperative diagnosis of periappendiceal abscesses, the presence of complicated appendicitis, and postoperative drainage. In the multivariate model, however, only the presence of complicated appendicitis remained significant in the development of IAA. This supports the claim that the nature of the AA itself is the strongest of all identified factors. Trying to explain these findings, we noted that among the perioperative parameters that might contribute to IAA formation, most of them are in fact related to the clinical picture of complicated appendicitis. For instance, higher CRP, higher WBC levels, and longer duration of symptoms, which were associated with IAA formation, are also associated with complicated appendicitis. Previous studies claimed that certain patient characteristics such as older age and diabetes mellitus may contribute to IAA occurrence; however, because these factors became insignificant in the multivariate logistic regression model, they cannot be considered independent risk factors. The only independent risk factor for IAA is complicated appendicitis. However, the data on the link of complicated AA and IAA are contradictory. The analysis by Cho et al. found no differences between complicated and uncomplicated appendicitis in terms of IAA [19]. In contrast, Schlottmann et al. observed higher incidence of IAA formation in patients with a gangrenous/perforated appendix [20].
Several strategies have been implemented to diminish the risk of IAA. Although the rate of patients with postoperative drainage was higher in the IAA group, we do not believe that peritoneal drainage itself contributed to IAA formation. Schlottmann et al. confirmed that drains are more often needed in cases of complicated appendicitis [20]. In our study, peritoneal drainage, while a risk factor in the univariate analysis, became insignificant in the multivariate model. According to a recent Cochrane review and other analyses, a no-drainage policy, even in complicated appendicitis, is safe and does not increase infectious complication rates [21–23].
Once IAA occurs, it certainly impacts postoperative outcomes. Almost two thirds of patients with IAA required reintervention after surgery, in the form of either percutaneous drainage or an operation. More than 50% of patients needed another operation. It is important to note that the majority of these surgically treated patients underwent relaparoscopy; in our opinion, this is feasible in patients with IAA without symptoms of general peritonitis.
Our study does have several limitations. Firstly, the majority of patients were assessed retrospectively. Only 30-day readmission rates to hospitals were analyzed, which may have impacted our stated rate of readmissions in both the IAA and non-IAA groups. Secondly, we did not analyze perioperative care protocols and operative techniques in each hospital. Although this may have some impact, LA is relatively straightforward, and it is rather unlikely that it significantly altered the outcomes. We did not observe an increased number of IAA in any of participating centers that would have suggested widely varying protocols between hospitals. Lastly, each hospital’s antimicrobial policy was also not analyzed in our database. This policy most likely did vary depending on the surgical unit. Although preoperative antibiotics have been shown to reduce complication rates, there is a lot of controversy as to whether they are of benefit in the postoperative period. The preventative effect of antibiotics in uncomplicated appendicitis is often negligible [24, 25], and, similarly, their use is being reduced in complicated cases as well [26]. Still, no good quality randomized controlled trials assess this aspect of perioperative care in complicated appendicitis.
Conclusions
Intraabdominal abscesses occurs rarely after LA and is strongly associated with complicated appendicitis. This complication greatly influences the postoperative period. Its treatment is associated with the need for reintervention, a prolonged length of stay, and possible readmission.
The members of the Pol-LA (Polish Laparoscopic Appendectomy) group are collaborators of the study:
Michał Pędziwiatr1,2, Kamil Astapczyk3, Maciej Bobowicz4, Mateusz Burdzel5, Karolina Chruściel6, Rafał Cygan7, Wojciech Czubek8, Natalia Dowgiałło-Wnukiewicz9, Jakub Droś10, Paula Franczak11, Wacław Hołówko12, Artur Kacprzyk10, Wojciech Konrad Karcz13, Jakub Kenig14, Paweł Konrad5, Arkadiusz Kopiejć15, Adam Kot15, Karolina Krakowska7, Maciej Kukla16, Anna Lasek1, Agnieszka Leszko7, Leszek Łozowski6, Piotr Major1,2, Wojciech Makarewicz4,15, Paulina Malinowska-Torbicz5, Maciej Matyja1, Judene Mavrikis1, Maciej Michalik9, Piotr Myśliwiec3, Adam Niekurzak17, Damian Nowiński3, Radomir Ostaszewski18, Małgorzata Pabis7, Małgorzata Polańska-Płachta5, Mateusz Rubinkiewicz1, Tomasz Stefura10, Anna Stępień19, Paweł Szabat20, Rafał Śmiechowski4, Sebastian Tomaszewski21, Viktor von Ehrlich-Treuenstätt13, Maciej Walędziak22, Maciej Wasilczuk8, Mateusz Wierdak1, Anna Wojdyła9, Jan Wojciech Wroński16, Michał Wysocki1,2, Leszek Zwolakiewicz23,24
1Jagiellonian University Medical College, 2nd Department of General Surgery, 21 Kopernika St, 31-501 Krakow, Poland
2Center for Research, Training and Innovation in Surgery (CERTAIN Surgery), 21 Kopernika St, 31-501 Krakow, Poland
3Medical University of Bialystok, 1st Department of General and Endocrinological Surgery, 24a M. Skłodowskiej-Curie St, 15-276 Bialystok, Poland
4Department of Surgical Oncology, Medical University of Gdansk, 17 Smoluchowskiego St, 80-211 Gdansk, Poland
5Medical University of Warsaw, Second Faculty of Medicine, 2nd Department of General, Vascular and Oncological Surgery, 19/25 Stępińska St, 00-739 Warsaw, Poland
6SPZOZ in Węgrów, Department of General Surgery, 201 Kościuszki St, 07-100 Węgrow, Poland
7Żeromski’s General Hospital, Department of General, Oncological and Minimal Invasive Surgery, 66 Na Skarpie, 31-913 Krakow, Poland
8Regional Hospital named J. Śniadecki, Department of General, Minimally Invasive and Oncology Surgery, 26 Skłodowska-Curie St, 15-278 Bialystok, Poland
9University of Warmia and Mazury in Olsztyn, Poland, Department of General, Minimally Invasive and Elderly Surgery, 44 Niepodleglosci St, 10-045 Olsztyn, Poland
10Jagiellonian University Medical College, Students’ Scientific Society of 2nd Department of General Surgery, 21 Kopernika St, 31-501 Krakow, Poland
11Ceynowa Hospital, Department of General and Oncological Surgery, 10 Jagalskiego St, 84-200 Wejherowo, Poland
12Medical University of Warsaw, Department of General, Transplant and Liver Surgery, Banacha 1a St, 02-097 Warszawa, Poland
13Ludwig Maximilian University, Clinic of General, Visceral and Transplantation Surgery, 15 Marchionini St, 81377 Munich, Germany
14Department of General, Oncologic and Geriatric Surgery, Jagiellonian University Medical College, 35-37 Pradnicka St, 31-202 Krakow, Poland
15Department of General Surgery and Surgical Oncology, Specialist Hospital in Kościerzyna, 36 Piechowskiego St, 83-400 Kościerzyna, Poland
16The Regional Subcarpathian John Paul II Hospital in Krosno, Department of General, Oncological and Vascular Surgery, 57 Korczyńska St, 38-400 Krosno, Poland
17Clinical Department of General Surgery with Oncology, Gabriel Narutowicz Memorial City Specialty Hospital, 35-37 Pradnicka St, 31-202 Krakow, Poland
18Municipal Hospital in Hajnówka, Department of General and Laparoscopic Surgery, 9 Dowgirda St, 17-200 Hajnówka, Poland
19Multispeciality Hospital in Nowa Sól, Department of General Surgery, 7 Chałubińskiego St, 67-100 Nowa Sol, Poland
20Leczna Hospital, Department of General and Minimally Invasive Surgery, 52 Krasnystawska St, 21-010 Leczna, Poland
21Dr Louis Błażek Memorial Hospital, Department of General Surgery, Oncological Surgery and Chemotherapy, 97 Poznańska St, 88-100 Inowroclaw, Poland
22Military Institute of Medicine, Department of General, Oncological, Metabolic and Thoracic Surgery, Szaserów 128 St, 00-141 Warsaw, Poland
23Faculty of Health Sciences, Powiślańska School in Kwidzyn, ul. 11 Listopada 29, 82-500 Kwidzyn, Poland
24Emergency Department, Specialist Hospital in Kościerzyna, 36 Piechowskiego St, 83-400 Kościerzyna, Poland