Emergency Medicine International

Emergency Medicine International / 2020 / Article

Research Article | Open Access

Volume 2020 |Article ID 4947192 | https://doi.org/10.1155/2020/4947192

Ji Ho Song, Yong Won Kim, Sanghun Lee, Han Ho Do, Jun Seok Seo, Jeong Hun Lee, Seung Chul Lee, "Clinical Difference between Acute Appendicitis and Acute Right-Sided Colonic Diverticulitis", Emergency Medicine International, vol. 2020, Article ID 4947192, 6 pages, 2020. https://doi.org/10.1155/2020/4947192

Clinical Difference between Acute Appendicitis and Acute Right-Sided Colonic Diverticulitis

Academic Editor: Roberto Cirocchi
Received30 Jun 2020
Revised29 Jul 2020
Accepted06 Aug 2020
Published01 Sep 2020


Background. Clinical presentations of acute appendicitis (AA) and acute right-sided colonic diverticulitis (ARCD) are similar. However, the usual treatment for each disease differs between surgical and conservative management. The aim of this study was to identify clinical differences between AA and ARCD. Method. We performed a single-center retrospective study on adult patients, with uncomplicated AA and ARCD confirmed by computed tomography, who visited an emergency department between March 2018 and August 2019. Clinical variables including past medical history, presented symptoms and signs, and laboratory findings were compared between the two groups. A logistic regression analysis was subsequently performed to differentiate ARCD from AA based on results of univariate analyses. Results. A total of 212 (79.1%) and 56 (20.9%) patients were enrolled in AA and ARSD groups, respectively. Logistic regression analysis revealed that a past history of diverticulitis [OR: 102.679 (95% CI: 9.964–1058.055), ] was associated with ARCD, while ketonuria [OR: 2.907 (95% CI: 1.091–7.745), ], anorexia [OR: 21.544 (95% CI: 3.905–118.868), ], and neutrophilia [OR: 3.406 (95% CI: 1.243–9.336), ] were associated with AA. Conclusion. Anorexia, neutrophilia, and ketonuria were predictors of AA while a history of diverticulitis was a predictor of ARCD.

1. Introduction

Acute appendicitis (AA) and acute right-sided colonic diverticulitis (ARCD) are inflammatory diseases that occur near anatomical locations. Their clinical presentations are similar, making it difficult to differentiate between them [13]. The current standard treatment for each disease is different. Appendectomy may be needed for AA while nonoperative conservative treatments such as bowel rest and/or antibiotics are usually used for uncomplicated diverticulitis [47]. Nevertheless, ARCD is often misdiagnosed as AA and revealed during surgery [3, 8]. Computer tomography (CT) can be used as a diagnostic imaging tool to avoid unnecessary surgical exploration or for ARCD mimicking AA [9]. However, it has the disadvantages of radiation exposure and cost. Although ultrasound is an alternative image modality to identify these two diseases without radiation hazard, it requires skillful users [10, 11]. Furthermore, episodes of diverticulitis are reported to recur in about 30% of cases. Abdominal image testing for each episode to differentiate between these two diseases can be a burden for the patient [6, 12]. In this respect, only a few studies have verified clinical differences between these two diseases [13, 14]. The purpose of this study was to identify different factors initially presented in the emergency room between AA and ARCD.

2. Materials and Methods

2.1. Study Design and Population

This single-center retrospective review study was conducted on consecutive Asian patients with age of 18 years old or older who visited the emergency department of a tertiary university hospital between March 2018 and August 2019 in the Republic of Korea, and diagnosis of AA or acute colonic diverticulitis was confirmed by a radiologist through an abdominal CT scan. Exclusion criteria were as follows: (1) patients had complications resulting from appendicitis and diverticulitis verified by CT scan (such as perforation, abscess, and/or fistula), (2) diverticulitis was not included in the right side of the colon, and (3) patients were transferred to another facility.

2.2. Study Variables

Clinical data obtained from electronic medical records included age, sex, body mass index (BMI), the time from symptom onset to visiting the emergency room, past medical history of previous diverticulitis or chronic diseases (diabetes, hypertension), gastrointestinal symptoms and signs (right lower quadrant [RLQ] pain, migrated pain to the RLQ, anorexia, nausea and vomiting, diarrhea), physical exams (initial body temperature, RLQ tenderness, rebound tenderness), laboratory findings (complete blood count, serum alanine transaminase [ALT], serum creatinine [Cr], serum C-reactive protein [CRP], urine ketone), Alvarado score and its components, and outcomes (need for hospitalization, length of stay, need for surgical treatment, mortality).

2.3. Study Definition

ARCD was defined as diverticulitis originating from primary inflammation of diverticulosis sited at the cecum or ascending colon. A history of diverticulitis was defined if patients were previously diagnosed with any sited colonic diverticulitis before the study period. Anorexia was defined as loss of appetite for food. Elevated ALT was defined as serum ALT over the upper limit of the normal value of 33 IU/L for males or 25 IU/L for females [15]. Elevated Cr was defined as serum Cr over the upper limit of the normal value of 1.29 mg/dL for males or 1.1 mg/dL for females [16]. Elevated CRP was defined as serum CRP concentration over 1.0 mg/dL, indicating significant inflammation [17]. Ketonuria was defined by a positive urine ketone dipstick test. The Alvarado score, a 10-point clinical scoring system, was calculated by adding each score to each clinical factor listed in Table 1 [18].


Nausea or vomiting1
Migrating pain to RLQ1
RLQ tenderness1
Rebound tenderness2
Elevated temperature (>37.3°)1
Leukocytosis >10,000/mm32
Neutrophilia >75%1

RLQ: right lower quadrant.
2.4. Statistical Analysis

Study variables of AA and ARCD groups were compared. Continuous variables are presented as median values (interquartile range, IQR). They were compared with the Mann–Whitney test. Nominal data were calculated as percentages based on the frequency of occurrence and compared using Chi-squared or Fisher’s exact test as appropriate. Multivariate logistic regression was used to correlate single variables with ARCD. Resulting odds ratios (ORs) and 95% confidence intervals (95% CIs) are presented. A two-sided value of less than 0.05 was considered statistically significant. All statistical analyses were performed using IBM Statistical Package for the Social Sciences (SPSS) software version 24.0 (SPSS, Inc., Chicago, IL, USA).

3. Results

During the study period, a total of 231 cases of acute appendicitis and 74 cases of acute colonic diverticulitis cases were diagnosed by abdominal CT scans of adult patients admitted to the emergency department. Among them, complicated cases (12 cases of appendicitis and 3 cases of diverticulitis), cases with non-right-side diverticulitis (n = 14), and cases that were transferred out (7 cases of acute appendicitis, 1 case of acute colonic diverticulitis) were excluded. Finally, 212 (79.1%) and 56 (20.9%) patients were enrolled in AA and ARCD groups, respectively.

Patient characteristics including clinical factors associated with each disease group and outcome are shown in Table 2. The AA group had more RLQ pain (94.3% vs. 85.7%, ), ketonuria (40.0% vs. 21.3%, ), anorexia (35.8% vs. 7.1%, ), RLQ tenderness (98.1% vs. 87.5%, ), rebound tenderness (40.1% vs. 25.0%, ), neutrophilia (62.7% vs. 37.5%, ), admission care (100% vs. 42.9%, ), and surgical treatment (99.1% vs. 0%, ) than the ARCD group. The AA group had higher percentage of neutrophils [78.6 (70.2–84.8) vs. 73.6 (67.1–77.0), ] and Alvarado scores [6 (4–7) vs. 5 (3–6), ] than the ARCD group. The ARCD group had longer onset-to-visit intervals [24 (13–48) vs. 11 (3–24) hours, ], more past histories of diverticulitis (23.2% vs. 0.9%, ), and higher percentage of lymphocytes [18.2 (13.8–24.9) vs. 14.1(9.3–22.0), ] than the AA group. There was no significant difference in other single clinical variables between the two groups.

ParametersTotal N = 268AA group N = 212 (79.1%)ARCD group N = 56 (20.9%)p value

Age (yr)40 (31–52)39 (30–53)41 (33–47)0.224
Male gender, no. (%)131 (48.9)107 (50.5)24 (42.9)0.368
BMI (kg/m2)23.3 (20.7–25.9)23.4 (20.9–25.9)22.4 (20.5–25.9)0.389
Onset-to-visit interval (hr)15 (4–47)11 (3–24)24 (13–48)<0.001

Past medical history
 Diabetes, no. (%)11 (4.1)8 (3.8)3 (5.4)0.704
 Hypertension, no. (%)18 (6.7)12 (5.7)6 (10.7)0.226
 History of diverticulitis, no. (%)15 (5.6)2 (0.9)13 (23.2)<0.001

Symptoms and signs
 Body temperature(°C)36.8 (36.5–37.3)36.8 (36.5–37.3)36.8 (36.5–37.1)0.432
 RLQ pain, no. (%)248 (92.5)200 (94.3)48 (85.7)0.042
 Diarrhea, no. (%)48 (17.9)34 (16.0)14 (25.0)0.169
 Constipation, no. (%)8 (3.0)4 (1.9)4 (7.1)0.062

Laboratory findings
 WBC11,470 (9,110–14,270)11,740 (9,155–14,550)11,160 (8,920–12,900)0.224
 Absolute neutrophil count8,860 (6,340–11,670)9,210 (6,410–11,830)7,960 (6,130–9,930)0.063
 Neutrophil (%)77.5 (69.1–83.3)78.6 (70.2–84.8)73.6 (67.1–77.0)<0.001
 Lymphocyte (%)14.8 (10.5–22.9)14.1 (9.3–22.0)18.2 (13.8–24.9)0.003
 Hb (g/dL)13.9 (12.7–14.9)14.0 (12.8–15.0)13.8 (12.3–14.7)0.374
 Hct (%)40.8 (37.5–43.9)40.8 (37.7–43.9)40.7 (36.9–43.8)0.920
 Elevated ALT, no. (%)36 (13.4)31 (14.6)5 (8.9)0.286
 Elevated Cr, no. (%)6 (2.2)5 (2.4)1 (1.8)1.000
 Elevated CRP, no. (%)155 (57.1)123 (58.0)32 (57.1)1.000
 CRP (mg/dL)1.5 (0.4–4.6)1.4 (0.3–4.2)2.2 (0.8–4.6)0.138
 Ketonuria, no. (%)90/247 (36.4)80/200 (40.0)10/47 (21.3)0.018

Alvarado score and components
 Alvarado score6 (4–7)6 (4–7)5 (3–6)<0.001
 Migration pain, no. (%)49 (18.3)44 (20.8)5 (8.9)0.051
 Anorexia, no. (%)90 (33.6)76 (35.8)4 (7.1)<0.001
 Nausea or vomiting, no. (%)92 (32.7)78 (35.1)14 (23.7)0.153
 RLQ tenderness, no. (%)257 (95.9)208 (98.1)49 (87.5)0.002
 Rebound tenderness, no. (%)99 (36.9)85 (40.1)14 (25.0)0.043
 Body temperature ≥37.3°C, no. (%)71 (26.5)59 (27.8)12 (21.4)0.396
 Leukocytosis, no. (%)179 (66.8)142 (67.0)37 (66.1)1.000
 Neutrophilia, no. (%)154 (57.5)133 (62.7)21 (37.5)0.001

 Admission care, no. (%)236 (88.1)212 (100)24 (42.9)<0.001
 Hospital days5 (4–6)5 (4–6)5 (4–6)0.574
 Surgical treatment, no. (%)211 (78.7)210 (99.1)0<0.001
 Mortality, no. (%)1 (0.4)1 (0.5)01.000

Median (interquartile range); AA: acute appendicitis; ARCD: acute right-sided colonic diverticulitis; BMI: body mass index; RLQ: right lower quadrant; WBC: white blood cell; Hb: hemoglobin; Hct: hematocrit; LDH: lactate dehydrogenase; ALT: alanine transaminase; Cr: creatinine; CRP: C-reactive protein.

Multivariate analysis revealed that factors predictive of ARCD were past history of diverticulitis [OR: 102.679 (95% CI: 9.964–1058.055), ], anorexia [OR: 0.046 (95% CI: 0.008–0.256), ], ketonuria [OR: 0.344 (95% CI: 0.129–0.961), ], and neutrophilia [OR: 0.294 (95% CI: 0.107–0.805), ] (Table 3).

Predictors of acute ARCDOdds ratio95% CI value

Onset-to-visit interval (hr)1.0000.999–1.0010.800
History of diverticulitis102.6799.964–1058.055<0.001
RLQ pain with tenderness0.3110.094–1.0290.056
Rebound tenderness0.4550.182–1.1380.092

CI: confidence interval; ARCD: acute right-sided colonic diverticulitis; AA: acute appendicitis; RLQ: right lower quadrant.

4. Discussion

Diverticulosis affects approximately 25.1% of Asian population. It accounts for 87.9% of colonic diverticulosis cases involving the right side. This percentage is significantly higher than that in Western countries [19]. ARCD has been reported to occur at a relatively young age. The overall prevalence of diverticulitis is 75% in Asian population [20, 21]. This study was limited to Asians. In the present study, 81.1% of colonic diverticulitis cases were ARCD cases. Our results showed that more surgical treatment was provided for AA, whereas conservative management was more provided for ARCD, consistent with a previous study [7]. Therefore, distinguishing these two diseases will be important for determining a therapeutic plan and avoiding unnecessary surgery for ARCD patients due to misdiagnosis or presumptive diagnosis as AA. The Alvarado scoring system is a classical tool for distinguishing appendicitis from other abdominal diseases [18]. However, even appendicitis can show equivocal Alvarado scores. Some studies have revealed that ARCD patients have higher or broader range of Alvarado scores [2224]. Therefore, it may not be enough to use this scoring system as a tool to distinguish between these diseases. Although Alvarado scores were different between the two groups in our single variable analysis (median value: 6 points for AA and 5 points for ARCD), it would be difficult to assign clinical meaning because scores of 5 to 6 have an equivocal probability for appendicitis [25]. Currently, few studies have reported clinical differences in symptoms and signs (such as longer symptom duration associated with ARCD and nausea or vomiting, anorexia, migration pain, and RLQ pain associated with AA) between AA and ARCD [13, 14, 22]. Most differences in symptoms might be due to different pathophysiologies and elapsing course of these two diseases. Although both diseases have similar final symptoms due to localized peritonitis, appendicitis has a sequential reaction with prodromal symptoms due to blockage and dilatation of the appendix first. The increase in intraluminal pressure then results in wall necrosis [26]. However, each subjective indicator might have a risk of bias by clinicians or patients. Otherwise, a few studies have reported that some laboratory factors (such as neutrophilia and high CRP) are associated with AA rather than ARCD [13, 14]. Like results of most previous studies, we found that a previous history of diverticulitis was a predictor of ARCD while anorexia and neutrophilia were predictors of AA.

An insufficient number of studies have reported the usefulness of leukocytosis for differentiating between the two diseases and, thus, it remains controversial [22, 27]. Shin et al. [13] have reported an elevated proportion of lymphocytes and a near-normal proportion of segmented neutrophils in ARCD. However, no hypothesis has been suggested to explain this phenomenon. Our results supported the relationship between neutrophilia and AA, and higher fractions of lymphocytes were also related to ARCD. Sasaki et al. [14] have categorized high serum CRP as > 3.0 mg/dL and reported that high serum CRP is associated with ARCD. However, our results did not support such finding. There was no statistical difference in the percentage of high serum CRP (32.5% vs. 37.5%, ) in our study between AA and ARCD groups, even when serum CRP values of over 3.0 mg/dL were used as criteria. Serum CRP is known to peak after 48 hours due to its response to inflammation [28]. Our study and the study by Sasaki et al. [14] differed in the time interval from onset-to-visit in the ARCD patients (24 h vs. 48 h). This could affect blood sample collection time after infection. Therefore, it might be inappropriate to compare these two studies. Moreover, it has been revealed that serum CRP levels will increase over time in appendicitis, raising question as to whether high CRP levels are more relevant to ARCD than to AA if confounding time factors related to CRP increase are not removed [29].

Our results revealed that ketonuria was one of the objective predictors of AA. We presented a boxplot for the distribution of urine ketone values between the two groups as shown in Figure 1. A few studies reported that ketonuria was seen in 12% to 45% of the AA cases, but there have been no comparative studies between AA and ARCD [30, 31]. Ketones are known as end-products of fatty acid metabolism. Ketonuria indicates that the body is excessively using fat over carbohydrates as the major source of energy [32]. Ketonuria could arise from dietary conditions (such as fasting, nausea and vomiting, and anorexia) and metabolic conditions (including type-1 diabetes, fever, and pregnancy) [33]. In our study, there were no patients with type-1 diabetes or pregnant women. There was no significant difference in body temperature between the two groups either. Therefore, the probable cause of ketonuria in appendicitis might be related to dietary conditions such as anorexia because these conditions were found more in the AA group than in the ARCD group. When we made a simple rule for predicting ARCD that included objective clinical factors such as no ketonuria and no neutrophilia with the presence of a history of diverticulitis, the calculated positive predictive value (PPV) was 87.5% (95% CI: 46.7–98.2%), the negative predictive value (NPV) was 95.2% (95% CI: 94.6–95.7%), and the specificity was 99.8% (95% CI: 99.3–99.9%). This rule might be a useful tool for distinguishing ARCD from AA.

This study has some limitations. First, this study was conducted on an Asian population at a single center in the Republic of Korea. Therefore, results of this study might not represent all races and nations. However, the presentation of diverticulitis in the Asian population is unusual because it most commonly involves the right side of the colon. The exact pathological mechanism of diverticular disease is unclear, although several theories related to genetics, diet, motility, and microbiome that might be affected by individual races and cultures have been presented [34]. Therefore, this study has some clinical implications because not many studies have been reported in an Asian population.

Second, because this study was a retrospective study rather than a confirmative study, data or cases might be missing. Specifically, for subjective symptoms and signs, it was difficult to accurately describe the intensity or presence without a proper prospective protocol.

Third, ketonuria is roughly correlated with serum ketone concentrations, but the absence of ketonuria does not mean the absence of blood ketone bodies. However, we could not obtain the serum ketone concentrations to distinguish between AA and ARCD as that analysis was not included in the routine ER blood tests because it is more expensive than urine analysis and has not been proven useful in the diagnosis of these diseases. Further studies that quantitatively analyze these factors are needed.

5. Conclusion

Our results suggest that anorexia, neutrophilia, and ketonuria are useful predictors of AA, but not ARCD. Conversely, a history of diverticulitis was a useful predictor of ARCD, but not AA. If a history of diverticulitis is present without neutrophilia or ketonuria, then the PPV is 87.5% and the specificity is 99.8% for ARCD. Our findings could be used for differential diagnosis between AA and ARCD to reduce unnecessary additional imaging studies for ARCD.

Data Availability

All datasets used and/or analyzed in the current study are available from the corresponding author upon reasonable request.

Ethical Approval

This study was approved by the Institutional Review Board (IRB) of Dongguk University Ilsan Hospital, Dongguk University (2018-11-007). Informed consent was waived by the IRB.

Conflicts of Interest

The authors declare that they have no conflicts of interest regarding the publication of this paper.


  1. O. Karatepe, O. Gulcicek, G. Adas et al., “Cecal diverticulitis mimicking acute Appendicitis: a report of 4 cases,” World Journal of Emergency Surgery, vol. 3, no. 1, p. 16, 2008. View at: Publisher Site | Google Scholar
  2. C. Y. Lo and K. W. Chu, “Acute diverticulitis of the right colon,” The American Journal of Surgery, vol. 171, no. 2, pp. 244–246, 1996. View at: Publisher Site | Google Scholar
  3. J. S. Lane, R. Sarkar, P. J. Schmit, C. F. Chandler, and J. E. Thompson, “Surgical approach to cecal diverticulitis,” Journal of the American College of Surgeons, vol. 188, no. 6, pp. 629–634, 1999. View at: Publisher Site | Google Scholar
  4. D. L. H. Baird, C. Simillis, C. Kontovounisios, S. Rasheed, and P. P. Tekkis, “Acute appendicitis,” BMJ, vol. 357, p. j1703, 2017. View at: Publisher Site | Google Scholar
  5. R. Detry, J. Jamez, A. Kartheuser et al., “Acute localized diverticulitis: optimum management requires accurate staging,” International Journal of Colorectal Disease, vol. 7, no. 1, pp. 38–42, 1992. View at: Publisher Site | Google Scholar
  6. M. M. Szojda, M. A. Cuesta, C. M. Mulder, and R. J. F. Felt-bersma, “Review article: management of diverticulitis,” Alimentary Pharmacology & Therapeutics, vol. 26, pp. 67–76, 2007. View at: Publisher Site | Google Scholar
  7. K. Matsushima, “Management of right-sided diverticulitis: a retrospective review from a hospital in Japan,” Surgery Today, vol. 40, no. 4, pp. 321–325, 2010. View at: Publisher Site | Google Scholar
  8. A. Sardi, A. Gokli, and J. A. Singer, “Diverticular disease of the cecum and ascending colon. a review of 881 cases,” The American Surgeon, vol. 53, no. 1, pp. 41–45, 1987. View at: Google Scholar
  9. B. A. Birnbaum and E. J. Balthazar, “CT of appendicitis and diverticulitis,” Radiologic Clinics of North America, vol. 32, no. 5, pp. 885–898, 1994. View at: Google Scholar
  10. Y.-H. Chou, H.-J. Chiou, C.-M. Tiu et al., “Sonography of acute right side colonic diverticulitis,” The American Journal of Surgery, vol. 181, no. 2, pp. 122–127, 2001. View at: Publisher Site | Google Scholar
  11. P. Rossi, P. Covarelli, F. Mosci, R. Bisacci, B. Sensi, and L. Moggi, “Ultrasonography in the management of acute appendicitis,” Surgical Endoscopy, vol. 10, no. 6, pp. 619–621, 1996. View at: Publisher Site | Google Scholar
  12. N. Stollman and J. B. Raskin, “Diverticular disease of the colon,” The Lancet, vol. 363, no. 9409, pp. 631–639, 2004. View at: Publisher Site | Google Scholar
  13. J.-H. Shin, B.-H. Son, and H. Kim, “Clinically distinguishing between appendicitis and right-sided colonic diverticulitis at initial presentation,” Yonsei Medical Journal, vol. 48, no. 3, pp. 511–516, 2007. View at: Publisher Site | Google Scholar
  14. Y. Sasaki, F. Komatsu, N. Kashima et al., “Clinical differentiation of acute appendicitis and right colonic diverticulitis: a case-control study,” World Journal of Clinical Cases, vol. 7, no. 12, pp. 1393–1402, 2019. View at: Publisher Site | Google Scholar
  15. J. K. Lee, J. H. Shim, H. C. Lee et al., “Estimation of the healthy upper limits for serum alanine aminotransferase in Asian populations with normal liver histology,” Hepatology, vol. 51, no. 5, pp. 1577–1583, 2010. View at: Publisher Site | Google Scholar
  16. C. Jones, G. McQuillan, J. Kusek et al., “Serum creatinine levels in the US population: third national health and nutrition examination survey,” American Journal of Kidney Diseases, vol. 32, no. 6, pp. 992–999, 1998. View at: Publisher Site | Google Scholar
  17. I. Kushner and M. J. Antonelli, “What should we regard as an “elevated” C-reactive protein level?” Annals of Internal Medicine, vol. 163, no. 4, p. 326, 2015. View at: Publisher Site | Google Scholar
  18. A. Alvarado, “A practical score for the early diagnosis of acute appendicitis,” Annals of Emergency Medicine, vol. 15, no. 5, pp. 557–564, 1986. View at: Publisher Site | Google Scholar
  19. C. C. Chan, K. L. Lo, E. C. H. Chung, S. S. Lo, and T. Y. W. Hon, “Colonic diverticulosis in Hong Kong: distribution pattern and clinical significance,” Clinical Radiology, vol. 53, no. 11, pp. 842–844, 1998. View at: Publisher Site | Google Scholar
  20. L. E. Hughes, “Postmortem survey of diverticular disease of the colon. I. Diverticulosis and diverticulitis,” Gut, vol. 10, no. 5, pp. 336–344, 1969. View at: Publisher Site | Google Scholar
  21. J.-K. Park, J.-K. Sung, S.-H. Choi, S.-S. Yun, and S. Lee, “Clinical analysis of right colon diverticulitis,” Annals of Surgical Treatment and Research, vol. 64, no. 1, pp. 44–48, 2003. View at: Google Scholar
  22. S. C. Chen, K. J. Chang, T. C. Wei, S. C. Yu, and S. M. Wang, “Can cecal diverticulitis be differentiated from acute appendicitis?” Journal of the Formosan Medical Association, vol. 93, no. 3, pp. 263–265, 1994. View at: Google Scholar
  23. F. Monari, M. Cervellera, B. Pirrera et al., “Right-sided acute diverticulitis: a single Western center experience,” International Journal of Surgery, vol. 44, pp. 128–131, 2017. View at: Publisher Site | Google Scholar
  24. R. McKay and J. Shepherd, “The use of the clinical scoring system by Alvarado in the decision to perform computed tomography for acute appendicitis in the ED,” The American Journal of Emergency Medicine, vol. 25, no. 5, pp. 489–493, 2007. View at: Publisher Site | Google Scholar
  25. C. D. Douglas, N. E. Macpherson, P. M. Davidson, and J. S. Gani, “Randomised controlled trial of ultrasonography in diagnosis of acute appendicitis, incorporating the Alvarado score,” BMJ, vol. 321, no. 7266, p. 919, 2000. View at: Publisher Site | Google Scholar
  26. J. M. Wagner, W. P. McKinney, and J. L. Carpenter, “Does this patient have appendicitis?” JAMA: The Journal of the American Medical Association, vol. 276, no. 19, pp. 1589–1594, 1996. View at: Publisher Site | Google Scholar
  27. N. S. Painter, “The cause of diverticular disease of the colon, its symptoms and its complications. Review and hypothesis,” Journal of the Royal College of Surgeons of Edinburgh, vol. 30, no. 2, pp. 118–122, 1985. View at: Google Scholar
  28. M. B. Pepys and G. M. Hirschfield, “C-reactive protein: a critical update,” Journal of Clinical Investigation, vol. 111, no. 12, pp. 1805–1812, 2003. View at: Publisher Site | Google Scholar
  29. H.-P. Wu, C.-Y. Lin, C.-F. Chang, Y.-J. Chang, and C.-Y. Huang, “Predictive value of C-reactive protein at different cutoff levels in acute appendicitis,” The American Journal of Emergency Medicine, vol. 23, no. 4, pp. 449–453, 2005. View at: Publisher Site | Google Scholar
  30. C.-Y. Chen, L.-L. Zhao, Y.-R. Lin, K.-H. Wu, and H.-P. Wu, “Different urinalysis appearances in children with simple and perforated appendicitis,” The American Journal of Emergency Medicine, vol. 31, no. 11, pp. 1560–1563, 2013. View at: Publisher Site | Google Scholar
  31. F. K. Althoubaity, “Suspected acute appendicitis in female patients,” Saudi Medical Journal, vol. 27, no. 11, pp. 1667–1673, 2006. View at: Google Scholar
  32. L. Laffel, “Ketone bodies: a review of physiology, pathophysiology and application of monitoring to diabetes,” Diabetes/Metabolism Research and Reviews, vol. 15, no. 6, pp. 412–426, 1999. View at: Publisher Site | Google Scholar
  33. J. A. Simerville, W. C. Maxted, and J. J. Pahira, “Urinalysis: a comprehensive review,” American Family Physician, vol. 71, no. 6, pp. 1153–1162, 2005. View at: Google Scholar
  34. L. L. Strate, R. Modi, E. Cohen, and B. M. R. Spiegel, “Diverticular disease as a chronic illness: evolving epidemiologic and clinical insights,” American Journal of Gastroenterology, vol. 107, no. 10, pp. 1486–1493, 2012. View at: Publisher Site | Google Scholar

Copyright © 2020 Ji Ho Song et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Related articles

No related content is available yet for this article.
 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles

No related content is available yet for this article.

Article of the Year Award: Outstanding research contributions of 2021, as selected by our Chief Editors. Read the winning articles.