Skip to main content
Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America logoLink to Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America
. 2020 Dec 1;71(Suppl 3):S232–S238. doi: 10.1093/cid/ciaa1309

Burden of Ileal Perforations Among Surgical Patients Admitted in Tertiary Care Hospitals of Three Asian countries: Surveillance of Enteric Fever in Asia Project (SEAP), September 2016–September 2019

Saqib H Qazi 1, Mohammad T Yousafzai 2, Nasir S Saddal 3, Irum F Dehraj 2, Rozina S Thobani 2, Afshan Akhtar 4, Jamal R Syed 3, Abdul M Kazi 2, Aneeta Hotwani 2, Najeeb Rahman 2, Junaid Mehmood 2, Jason R Andrews 5, Stephen P Luby 5, Denise O Garrett 6, Farah N Qamar 2,
PMCID: PMC7705870  PMID: 33258928

Abstract

Background

Typhoid fever is caused by Salmonella enterica subspecies enterica serovar Typhi (S. Typhi) and can lead to systemic illness and complications. We aimed to characterize typhoid-related ileal perforation in the context of the population-based Surveillance of Enteric Fever in Asia Project (SEAP) in Bangladesh, Nepal and Pakistan.

Methods

Between September 2016 and September 2019, all cases of nontraumatic ileal perforation with a clinical diagnosis of typhoid were enrolled from 4 tertiary care hospitals in Karachi, 2 pediatric hospitals in Bangladesh, and 2 hospitals in Nepal. Sociodemographic data were collected from patients or their caregivers, and clinical and outcome data were retrieved from medical records. Tissue samples were collected for histopathology and blood cultures where available.

Results

Of the 249 enrolled cases, 2 from Bangladesh, 5 from Nepal and 242 from Pakistan. In Pakistan, most of the cases were in the 0–15 (117/242; 48%) and 16–30 (89/242; 37%) age groups. In all countries, males were most affected: Pakistan 74.9% (180/242), Nepal 80% (4/5), and Bangladesh 100% (2/2). Blood culture was done on 76 cases; 8 (11%) were positive for S. Typhi, and all were extensively drug resistant (XDR) S. Typhi. Tissue cultures was done on 86 patients; 3 (3%) were positive for S. Typhi, and all were XDR S. Typhi, out of 86 samples tested for histopathology 4 (5%) revealed ileal perforation with necrosis. Culture or histopathology confirmed total 15 (11%) enteric fever cases with ileal perforation are similar to the clinically diagnosed cases. There were 16/242 (7%) deaths from Pakistan. Cases of ileal perforation who survived were more likely to have sought care before visiting the sentinel hospital (P = .009), visited any hospital for treatment (P = .013) compared to those who survived.

Conclusions

Although surveillance differed substantially by country, one reason for the higher number of ileal perforation cases in Pakistan could be the circulation of XDR strain of S. Typhi in Karachi.

Keywords: enteric perforation, ileal perforation, Salmonella Typhi, enteric fever, typhoid fever


Typhoid fever caused by Salmonella enterica subspecies enterica serovar Typhi (S. Typhi) can lead to systemic illness that has been a major source of morbidity and mortality in low-income communities [1]. Despite advancements in medical treatment, addressing typhoid fever remains difficult in many parts of the world such as South Asia, where poor water supply and sanitation remain a major problem [2, 3]. In such settings, incidence can be as high ≥10 cases per 100 000 population per year, and 1 in 5 children experiences typhoid infection by the age of 10 years [4, 5]. An important factor in decreasing the burden of typhoid fever has been the emergence of antibiotic resistance [6]. Multidrug resistant (MDR) strains of S. Typhi, resistant to ampicillin, trimethoprim-sulfamethoxazole (TMP-SMZ), and chloramphenicol have increased dramatically in the last 2 decades [7]. More recently, extensively drug resistant (XDR) strains have been isolated in Pakistan that are resistant to ampicillin, TMP-SMZ, fluoroquinolones, and third-generation cephalosporins, leaving limited treatment options for typhoid treatment [8]. Untreated typhoid disease can lead to altered mental states (termed the typhoid state), ileus, gastrointestinal bleeding, ileal perforation septic shock, and death [1, 9, 10]. Ileal perforation is a fatal complication that usually occurs in the second or third week of illness, due to inflammation and necrosis of Peyer’s patches. However, it has also been reported in the second week of illness in lower middle-income countries [11–14]. Typhoid related ileal perforation has been reported in 0.8%–39% of typhoid patients [15–17] with a higher incidence in low- and middle-income countries [18, 19]. Reported mortality rates due to ileal perforation range from 5% in wealthy regions to 80% in poor regions [20, 21]. The burden of typhoid related ileal perforation has been attributed to these factors: increasing antibiotic resistance, delay in diagnosis, delay in surgical treatments, inappropriate surgical technique and nonavailability of guidelines for appropriate postoperative care [22]. The emergence of antimicrobial resistance, especially XDR strains of S. Typhi in Pakistan, may increase the risk of typhoid perforation. The lack of availability of antimicrobial sensitivity testing and limited understanding of its importance in most secondary level hospitals and first level care facilities can increase the delay in initiating the appropriate course of antimicrobial therapy and increase the risk of treatment failures.

With worsening antimicrobial resistance, it is important to assess the burden and consequences of typhoid related ileal perforation. We aim to describe the frequency of typhoid related ileal perforation and attributed mortality from a multicenter, prospective surveillance project in 3 Asian countries.

METHODS

Study Design and Settings

This prospective surveillance study was part of the Surveillance for Enteric Fever in Asia Project (SEAP) conducted at different hospitals and lab networks in Bangladesh, Nepal, and Pakistan from September 2016 to September 2019 [23]. For the enrollment of surgical cases in Bangladesh, the study was conducted in Dhaka Shishu (Children’s) Hospital and Shishu Shasthya Foundation Hospital. Both serve the pediatric population. In Nepal the study was conducted in Dhulikhel Hospital and Kathmandu Medical College and Teaching Hospital, which serves both adult and pediatric population. In Pakistan we selected JinnahPostgraduate Medical Center (JPMC), the National Institute of Child Health (NICH), Aga Khan University Hospital (AKUH),and Kharadar General Hospital (KGH). These included bothpublic and private tertiary care facilities serving adults, pediatric populations, or both. All site hospitals public and private were purposefully selected to include patients with diverse socioeconomic background and logistical accessible. Enrollment of typhoid-related ileal perforation cases was initiated in September 2016 at AKUH and KGH, in November 2016 at NICH, and in February 2018 at JPMC. In Nepal and Bangladesh, the enrollment was started in September 2016 at all of their sites.

Eligibility Criteria

All hospitalized cases with a diagnosis of nontraumatic ileal perforation due to suspected typhoid were identified from the daily census sheets of the respective surgical units in the selected hospitals.

The diagnosis of typhoid perforation was made by the admitting surgeon and was mainly clinical, supplemented by intraoperative findings of acute, inflamed, terminal ileal perforation. Patients with ileal perforation due to tuberculosis and malignancy identified perioperatively or on subsequent tissue histopathology were excluded.

Enrollment and Data Collection

Trained research associates with nursing or medical background approached the patient under the supervision of a surgeon used a structured questionnaire to collect sociodemographic data through a face-to-face interview with either the adult patient or the caregiver of a child. The clinical diagnosis, surgical record, and outcome were obtained from the patients’ medical records. The medical records were reviewed daily to identify any change in the diagnosis. Close coordination and liaison were established with all surgeons in the respective units of the selected hospitals. Detailed data on the sociodemographic and clinical characteristics was collected from all surgical enrolled patients from all countries. Information from the questionnaire and medical records was directly entered into the tablets. Follow-up of all patients was done through phone calls 6 weeks after enrollment. Information about outcome (survival/death) and recovery was collected during 6 week follow-up.

Data Management

The tablets’ electronic data collection system automatically assigned a unique identification number to the data of each participant. The research supervisor cross-checked each questionnaire for any errors or an inconsistent response at the end of the day before syncing the data into the central database.

Laboratory Testing and Procedures

After enrollment of the patient, blood culture was collected and then treatment was initiated. The trained research staff collected 5–10 mL of the blood sample and submitted to clinical laboratory of AKUH for testing. During surgery, the operating surgeon obtained tissue samples in normal saline and provided them to the study staff for histopathology testing. The study staff delivered the tissue samples to the Infectious Diseases and Research Laboratory (IDRL) of Aga Khan University for culture and histopathology testing. Ultrasound or any other tests needed for the confirmation of the perforation were performed at the discretion of the operating surgeon.

Data Analysis

Data were retrieved directly from the server, and descriptive statistics were calculated for both continuous and categorical variables. For continuous variables, the mean with standard deviation were calculated. For categorical variables, frequency with percentages was calculated. Factor analysis of ileal perforation patients’ household possessions was performed to determine socioeconomic status (SES). Factors with high eigenvalues were considered to classify SES and generate scores. These were then divided into 3 quintiles. Trends of ileal perforation across different age groups were analyzed. A comparison of the recovered versus those who died was analyzed. The number of ileal perforation across different age groups were plotted in a line graph, and comparison of the survivors versus nonsurvived was analyzed using Pearson χ 2 or Fisher exact test to calculate the P values. A P value of < .05 was considered statistically significant. In order to evaluate whether culture or histopathology confirmed enteric fever cases with ileal perforation are similar to the clinically diagnosed cases, we performed a sensitivity analysis as reported in Supplementary Table 1. P values were calculated using χ 2 or Fisher exact test for categorical and independent sample t test for quantitative variables.

Ethical Consideration

Trained research associates with nursing or medical background approached the patients and/or their attendants and informed consent and/or assent was sought before the enrollment. We obtained written informed consent from all adult patients (age 18 years and above). For all patients aged < 11 years consent was taken from their parents or legal guardians. For patients aged 11–17 years, assent along with parental consent was also obtained. Each individual participant had the right to withdraw her/his consent at any time. Confidentiality was maintained by the assigning unique identifier number, and no personal identifying details such as name was obtained. The study was approved by the ethical review committees (ERC) of the Bangladesh Institute of Child Health, Nepal Health Research Council, Aga Khan University, National Bioethics committee (NBC) Pakistan and Stanford University.

RESULTS

During September 2016 to September 2019 a total of 249 patients with ileal perforation were enrolled: 242 from Pakistan, 2 cases from Bangladesh, and 5 from Nepal. In all 3 countries males were most affected: Pakistan 180/242 (74.9 %); Bangladesh 2/2 (100%); and Nepal 4/5 (80%). In Pakistan, 54% (130/242) of typhoid related ileal perforation were enrolled during 2018 and 30% in 2019 (73/242). Of the typhoid-related ileal perforation cases 41% (99/242) were in the first SES quintile, and 39% (94/242) were in the third quintile (Table 1).

Table 1.

Sociodemographic and Clinical Characteristics of Patients With Enteric Perforation in Pakistan, Nepal, and Bangladesh, Surveillance for Enteric Fever in Asia Project (SEAP), 2016–2019 (N = 249)

Sociodemographic Variables Pakistan Nepal Bangladesh
N = 242 (%) N = 5 (%) N = 2 (%)
Age in years
 0–15 117 (48) 1 (20) 2 (100)
 16–30 89 (37) 1 (20) 0 (0)
 >30 36 (15) 3 (60) 0 (0)
Sex
 Male 180 (75) 4 (80) 2 (100)
Clinical characteristics Median (IQR)
 Duration of illness before hospitalization 11 (6,18)
 Duration of hospitalization 8 (6,13)
 Fever 234 (97)
 Abdominal pain 224 (93)
 Constipation/diarrhea 137 (57)
 Vomiting 148 (61)
Health-seeking behavior
 Patient sought any care from somewhere else before enrollment visit 219 (91)
 Treatment from any hospital 163 (67)
 Treatment from pharmacy, clinic or physician 134 (55)
 Received treatment from traditional healer 10 (4)
Prior treatment N = 208
 Antibiotic 141 (58)
 Antipyretic 194 (80)
 Analgesic 123 (51)
 Antidiarrheal 16 (7)
Patients receiving antibiotics during hospitalization N = 236 (%)
 Type of antibiotics
 Cephalosporin 86 (36)
 Piperacillin and tazobactam 23 (10)
 Ciprofloxacin 34 (14)
 Metronidazole 33 (14)
 Carbapenem 34 (14)
 Other 26 (11)
Chest X-ray N = 242 (%)
 Performed 177 (73)
 Indicated but not performed/ missing/not indicated 65 (27)
Abdominal ultrasound finding N = 146 (%)
 Internal bleeding/intestinal hemorrhage 17 (12)
 Intestinal perforation 114 (78)
 Hepatomegaly/splenomegaly 23 (16)
 Peritonitis 70 (48)
 Other 54 (37)
Blood culture positive for S. Typhi 8/76 (11) 1/3 (33)
MDR 0 0
XDR 8 (100) 0
Tissue culture N = 86 (%)
 NICH 57 (66)
 JPMC 29 (34)
 Tissue culture positive for S. Typhi 3 (3)
 Histopathology confirmed Ileal perforation with necrosis 4 (5)
 Blood/ tissue culture/ histopathology positive for S. Typhi (individuals) 15/131 (11)
Hospital where surgery performed N = 242 (%)
 AKUH/KGH 19 (8)
  NICH 103 (42)
 JPMC 120 (50)
Final outcome at discharge N = 242 (%) n = 5 (%) n = 2 (%)
 Recovered 226 (93) 5 (100) 2 (100)
 Died 16 (7) 0 (0) 0 (0)
Social and economic status
Wealth status scores (tertile) N = 242 (%)
 Low wealth status 99 (41)
 Medium wealth status 49 (20)
 High wealth status 94 (39)
Year of surveillance N = 242 (%)
 2016 4 (2)
 2017 35 (14)
 2018 130 (54)
 2019 73 (30)

Abbreviations: AKUH, Aga Khan University Hospital; JPMC, Jinnah Postgraduate Medical Center; IQR, interquartile range; KGH, Kharadar General Hospital; MDR, multidrug resistant; NICH, National Institute of Child Health; XDR, extensively drug resistant.

The median (interquartile range [IQR]) duration of illness prior to hospitalization was 11 (6, 18) days, and the duration of hospitalization was 8 (6, 13) days. Fever, abdominal pain, constipation/diarrhea, and vomiting were the common clinical characteristics of the patients: 91% (219/242) sought care prior to hospitalization and 58% (142/242) self-reported that they had received an antibiotic before presenting to the hospital. Blood culture was done on 76 cases; 8 (11%) were positive for S. Typhi and all were XDR S. Typhi. Tissue culture was done on 86 patients; 3 (3%) were positive for S. Typhi, and all were XDR S. Typhi. Culture or histopathology confirmed 15 (11%) ileal perforation cases were statistically similar to clinically diagnosed ileal perforations in terms of sociodemographic characteristics, clinical symptoms at the time of presentation, and final outcome at discharge. Only the occurrence of 1 or more clinical symptoms was statistically significant (Supplementary Table 1). Of the typhoid related ileal perforation cases from Pakistan, there were 16/242 (7%) deaths; 10 were aged 0–15 years. Among recovered patients, the median and IQR of the duration of illness prior to hospitalization was 11 (6, 17); of those who died it was 15 (10, 28) days.

Cases of typhoid related ileal perforation who recovered as compared to those who died were more likely to seek care before visiting the sentinel hospital (92% vs 69%; P = .009) and more likely to visit other hospitals for treatment (68% vs 63%; P = .013). No other significant difference in terms of clinical or sociodemographic characteristics between the two groups were identified (Table 2). The frequency of ileal perforation was highest in all age groups in 2018, followed by 2019 and 2017. The pattern of typhoid related ileal perforation was similar in 2018 and 2019, with highest frequency in the age group 15–25 followed by 5–10 years old; however, in 2017 the highest number of ileal perforation occurred among 5–10 years old age group only (Figure 1).

Table 2.

Comparison of Patients With Enteric Perforation Who Died Versus Those Who Survived in Pakistan, Surveillance for Enteric Fever in Asia Project (SEAP), 2016–2019

Sociodemographic Variables Recovered Died P value
N = 226 (%) N = 16 (%)
Age in years
 0–15 107 (48) 10 (62) .035
 16–30 87 (38) 2 (13)
 >30 32 (14) 4 (25)
Sex
 Male 171 (76) 9 (56) .086
 Female 55 (24) 7 (44)
Clinical characteristics Median (IQR) Median (IQR)
 Duration of illness before hospitalization 11 (6,17) 15 (10,28) .635
 Duration of hospitalization 8 (6,13) 8 (4,19) .488
N (%)
 Fever 219 (97) 15 (94) .495
 Abdominal pain 208 (92) 16 (100) .502
 Constipation / diarrhea 123 (54) 14 (88) .010
 Vomiting 134 (59) 14 (88) .081
Health-seeking behavior
 Patient sought any care from somewhere else before enrollment visit 208 (92) 11 (69) .009
 Received treatment from any hospital 153 (68) 10 (63) .013
 Received treatment from any pharmacy, clinic, and physician 125 (55) 9 (56) .942
 Received treatment from traditional healer 9 (4) 1 (6) .019
Prior treatment
 Patient received antibiotic 132 (58) 9 (56) .338
 Patient received antipyretic and analgesic 185 (82) 12 (75) .496
 Patient received antidiarrheal prior 15 (7) 1 (6) .354
 Patients receiving antibiotics during hospitalization 221 (98) 15 (94) .164
Type of antibiotics
 Cephalosporin 31 (14) 3 (20) .590
Piperacillin and tazobactam 79 (36) 7 (47) .575
 Ciprofloxacin 33 (15) 1 (7) .430
 Metronidazole 33 (15) 0 (0) .136
 Carbapenem 24 (11) 2 (13) .793
 Other 21 (10) 2 (13) .665
Chest X-ray N = 226 (%) N = 16 (%)
 Performed 163 (72) 14 (88) .180
 Indicated, but not performed/ missing and not indicated 63 (28) 2 (12)
Abdominal ultrasound performed 136 (60.2) 10 (62.5) .854
Ultrasound finding
 Internal bleeding/intestinal hemorrhage 16 (12) 1 (10) .867
 Intestinal perforation 107 (79) 7 (70) .522
 Hepatomegaly and splenomegaly 20 (15) 3 (30) .200
 Peritonitis 67 (49) 3 (30) .239
Blood culture
S. Typhi 8 (11) 0 .426
Hospital where surgery performed N = 226 (%) N = 16 (%)
 AKUH/KGH 19 (8) 0 (0) .247
 NICH 94 (42) 9 (56.3) .486
 JPMC 113 (50) 7 (43.8) .775
Social and economic status
Wealth status scores (tertile) N = 226 (%) N = 16 (%)
 Low wealth status 92 (41) 7 (44) .723
 Medium wealth status 47 (21) 2 (13)
 High wealth status 87 (38) 7 (44)

Abbreviations: AKUH, Aga Khan University Hospital; IQR, interquartile range; JPMC, Jinnah Postgraduate Medical Center; KGH, Kharadar General Hospital; NICH, National Institute of Child Health.

Figure 1.

Figure 1.

Trend of ileal perforation across different age groups, Karachi, Pakistan, Surveillance for Enteric Fever in Asia Project (SEAP), 2016–2019.

DISCUSSION

We conducted surveillance in three large cities in Bangladesh, Nepal, and Pakistan for ileal perforation. The surveillance in Karachi included 2 additional hospitals specifically to look for perforations. Compared with Bangladesh and Nepal, we observed more ileal perforation cases in Pakistan, at a time when there was widespread circulation of XDR typhoid. Due to the unavailability of sensitive tool for the diagnosis of typhoid-related ileal perforation, in this study all cases were diagnosed based on intraoperative findings supplemented with clinical sign and symptoms. Blood cultures were sent by the treating physicians in only a small proportion of the cases; the tissue samples either were not collected at the time of surgery, or tissue samples were collected in formalin hindering culture. Only a minority cases of ileal perforation were confirmed through blood and tissue cultures and histopathology testing. Traditionally, diagnosis is made mainly on the basis of clinical history and examination, X-ray abdomen, and ultrasound abdomen. Although serologic and bacteriologic data may be supportive, these are frequently negative. Blood cultures are positive for S. Typhi in only 3–34% of cases of typhoid perforation, and cultures of the stool and peritoneal fluid are usually negative for this organism [24]. Although surgical diagnosis of typhoid related ileal perforation is not 100% sensitive or specific, this is the most frequently reported method for the diagnosis of typhoid-related ileal perforation in the existing literature. Most of the earlier studies reported from African countries were based on confirmation on Widal test or clinical suspicion, which is known to have poor sensitivity and specificity [25–28]. Polymerase chain reaction (PCR) based testing and immunohistochemical staining of the tissue as a tool for diagnosis of typhoid-related ileal perforation is currently under investigation and might improve the diagnosis in future.

Differences in the surveillance sites could partly explain the high number of cases from Pakistan. Although the SEAP surveillance sites were used to enroll ileal perforation cases from Bangladesh and Nepal, in Pakistan (in addition to the SEAP surveillance sites) 2 additional public sector tertiary care referral hospitals were used. Being public sector referral hospitals, patients were from lower socioeconomic backgrounds and also from the very remote areas of Sindh province. Another contributing explanation to the larger number of cases in Pakistan could be the difference in antibiotic resistance patterns, especially XDR strains of S. Typhi in the 3 countries. Pakistan is the only country among the SEAP sites where XDR typhoid fever is prevalent Yousafzai et al Pakistan budren paper in this supplement (S214). In addition, the minority of the blood samples from the patients with ileal perforation from Pakistan from which S. Typhi were isolated, all were XDR. Therefore, a higher proportion of XDR typhoid cases in Pakistan might have contributed to the higher number of typhoid-related ileal perforation. Whether the higher number of ileal perforation cases in Pakistan as compared to the other 2 countries is the function of XDR outbreak of Salmonella Typhi in Pakistan or just the reflection of how and where the surveillance was conducted in these 3 countries is hard to conclude [29]. A 2-year surveillance study in Tanzania during 2006–2008 enrolled 104 typhoid-related ileal perforation cases. The study reported male preponderance and higher incidence in the age group 11–20 years old [26]. In contrast, a study from India during 2015–2017, reported higher proportions of typhoid-related ileal perforation among adults aged 31–40 years [30]. Nonetheless, males being at higher risk of typhoid-related ileal perforation is consistent with reports from India and several other countries [31, 32]. Only 1 study from Nigeria reported a higher number of ileal perforation cases among female populations [33]. The exact mechanism behind male preponderance for ileal perforation is not known. However, there might be a genetic predisposition among males that heightens the risk of ileal perforation [34]. Another reason could be the higher proportion of culture confirmed typhoid cases among the male population as compared to females. SEAP data from Pakistan showed significantly higher proportion of culture confirmed typhoid among the male population Yousafzai et al paper in this supplement.

In this study, the duration of illness among patients with ileal perforation was >10 days before hospitalization. Typhoid-related ileal perforation classically presents in the second week of illness, and hospitalization for typhoid-associated ileal perforation is normally long, ranging from 2 to 4 weeks. The duration of hospitalization is dependent on the condition of the patient at the time of admission and postoperative complications [33, 35–37].

Studies from other countries also reported delayed presentation and poor socioeconomic status as an important predictor of enteric perforations and its associated mortality [22]. In this study, 16 deaths (7%) were observed among typhoid-related ileal perforation in Pakistan. Duration of illness, socioeconomic status, and prior use of antibiotics was not associated with mortality. However, mortality was significantly higher among children (<15 years old). The reported mortality ranged from 4% in northern part of India to as high as 34% in parts of sub-Saharan Africa [33, 38]. Mortality associated with enteric perforations can be prevented with early diagnosis and treatment, access to surgical care, availability of better surgical facilities, trained surgeons, and prevention of postoperative complications [39]. Unfortunately, limitations in healthcare in general and surgical care in particular is lacking in lower and middle-income countries and can result in delays in accessing care and subsequent peri- or postoperative mortalities [22].

Our study had several limitations; a larger number of cases were identified from Pakistan presumably because this was the only site that had 2 surgical units of large public sector hospitals included as sentinel sites for enrollment. Only a subset of the cases could be confirmed through blood cultures and histopathological examination of the tissues, and hence some misclassification might have occurred. However, clinical suspicion of typhoid based on a history of fever for more than a week, followed by perforation was used as a criterion for clinical suspicion of typhoid-related ileal perforation and the intraoperative findings of the surgeons verified the diagnosis. The absence of a sensitive tool to confirm typhoid-related ileal perforation might have resulted in some classification bias resulting in over-estimation of cases in this study. However, the study team worked closely with the operating surgeons to minimize any bias in diagnosis. Patients with ileal perforation due to tuberculosis and malignancy identified perioperatively or on subsequent tissue histopathology were excluded. Patients with typhoid-related ileal perforation who presented as dead or who died immediately after reaching the emergency department of the respective hospitals and could not be operated or diagnosed were not accounted for in this study, and hence the case fatality rate might have been underestimated.

CONCLUSIONS

Cases of typhoid-related ileal perforation were identified mainly in Pakistan; however, because of lack of availability of sensitive diagnostic tools, a bacteriologic diagnosis was not possible in most cases. Early diagnosis and treatment are essential for adequate management of ileal perforation in typhoid endemic countries. The development of improved tools to specify the cause of intestinal perforation would permit better understanding and tracking of this important occasional consequence of Salmonella typhoid and paratyphoid infection.

Supplementary Data

Supplementary materials are available at Clinical Infectious Diseases online. Consisting of data provided by the authors to benefit the reader, the posted materials are not copyedited and are the sole responsibility of the authors, so questions or comments should be addressed to the corresponding author.

ciaa1309_suppl_Supplementary_Table_1

Notes

Financial support. This work was supported by Bill & Melinda Gates Foundation (Investment ID 008335). S. P. L. and J. A. report grants from Gates Foundation, during the conduct of the study.

Supplement sponsorship. This supplement is sponsored by the Sabin Vaccine Institute and made possible by a grant from the Bill & Melinda Gates Foundation.

Potential conflicts of interest. The authors: No reported conflicts of interest. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest.

References

  • 1. James SL, Abate D, Abate KH, et al.  Global, regional, and national incidence, prevalence, and years lived with disability for 354 diseases and injuries for 195 countries and territories, 1990–2017: a systematic analysis for the Global Burden of Disease Study 2017. Lancet 2018; 392:1789–858. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2. Bhutta ZA, Gaffey MF, Crump JA, et al.  Typhoid fever: way forward. Am J Trop Med Hyg 2018; 99:89–96. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3. Stanaway JD, Reiner RC, Blacker BF, et al.  The global burden of typhoid and paratyphoid fevers: a systematic analysis for the Global Burden of Disease Study 2017. The Lancet Infect Dis 2019; 19:369–81. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4. Qamar FN, Azmatullah A, Bhutta ZA. Challenges in measuring complications and death due to invasive Salmonella infections. Vaccine 2015; 33(Suppl 3):C16–20. [DOI] [PubMed] [Google Scholar]
  • 5. Breiman RF, Cosmas L, Njuguna H, et al.  Population-based incidence of typhoid fever in an urban informal settlement and a rural area in Kenya: implications for typhoid vaccine use in Africa. PLoS One 2012; 7:e29119. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6. Cantón R, Morosini MI. Emergence and spread of antibiotic resistance following exposure to antibiotics. FEMS Microbiol Rev 2011; 35:977–91. [DOI] [PubMed] [Google Scholar]
  • 7. Yang Y-A, Chong A, Song J. Why is eradicating typhoid fever so challenging: implications for vaccine and therapeutic design. Vaccines 2018; 6:45. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Klemm EJ, Shakoor S, Page AJ, et al.  Emergence of an extensively drug-resistant Salmonella enterica serovar Typhi clone harboring a promiscuous plasmid encoding resistance to fluoroquinolones and third-generation cephalosporins. MBio 2018; 9:e00105–18. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9. Harris JB, Brooks WA. Typhoid and paratyphoid (enteric) fever. In Hunter’s tropical medicine and emerging infectious diseases 2020:608–16. Content Repository Only!. [Google Scholar]
  • 10. Bhutta ZA. Impact of age and drug resistance on mortality in typhoid fever. Arch Dis Child 1996; 75:214–7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11. Acosta C, Albert J, Bhan M.  Background document: The diagnosis, treatment, and prevention of typhoid fever. Geneva, Switzerland: World Health Organization, 2003:7. [Google Scholar]
  • 12. Uba AF, Chirdan LB, Ituen AM, Mohammed AM. Typhoid intestinal perforation in children: a continuing scourge in a developing country. Pediatr Surg Int 2007; 23:33–9. [DOI] [PubMed] [Google Scholar]
  • 13. Rahman GA, Abubakar AM, Johnson AW, Adeniran JO. Typhoid ileal perforation in Nigerian children: an analysis of 106 operative cases. Pediatr Surg Int 2001; 17:628–30. [DOI] [PubMed] [Google Scholar]
  • 14. Ameh EA. Typhoid ileal perforation in children: a scourge in developing countries. Ann Trop Paediatr 1999; 19:267–72. [DOI] [PubMed] [Google Scholar]
  • 15. Atamanalp SS, Aydinli B, Ozturk G, Oren D, Basoglu M, Yildirgan MI. Typhoid intestinal perforations: twenty-six year experience. World J Surg 2007; 31:1883–8. [DOI] [PubMed] [Google Scholar]
  • 16. Eggleston FC, Santoshi B, Singh CM. Typhoid perforation of the bowel: experiences in 78 cases. Ann Surg 1979; 190:31–5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17. Butler T, Knight J, Nath SK, Speelman P, Roy SK, Azad MA. Typhoid fever complicated by intestinal perforation: a persisting fatal disease requiring surgical management. Rev Infect Dis 1985; 7:244–56. [DOI] [PubMed] [Google Scholar]
  • 18. Worku B. Typhoid fever in an Ethiopian children’s hospital: 1984–1995. Ethiop J Health Dev 2000; 14(3): 311–6. [Google Scholar]
  • 19. Chiu CH, Tsai JR, Ou JT, Lin TY. Typhoid fever in children: a fourteen-year experience. Acta Paediatr Taiwan 2000; 41:28–32. [PubMed] [Google Scholar]
  • 20. Sümer A, Kemik O, Dülger AC, et al.  Outcome of surgical treatment of intestinal perforation in typhoid fever. World J Gastroenterol 2010; 16:4164–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21. Mock CN, Amaral J, Visser LE. Improvement in survival from typhoid ileal perforation: results of 221 operative cases. Ann Surg 1992; 215:244–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22. Contini S. Typhoid intestinal perforation in developing countries: still unavoidable deaths? World J Gastroenterol 2017; 23:1925–31. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23. Andrews JR, Barkume C, Yu AT, et al.  Integrating facility-based surveillance with healthcare utilization surveys to estimate enteric fever incidence: methods and challenges. J Infect Dis 2018; 218:268–76. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24. Keenan JP, Hadley GP. The surgical management of typhoid perforation in children. Br J Surg 1984; 71:928–9. [DOI] [PubMed] [Google Scholar]
  • 25. Osifo OD, Ogiemwonyi SO. Typhoid ileal perforation in children in Benin city. Afr J Paediatr Surg 2010; 7:96–100. [DOI] [PubMed] [Google Scholar]
  • 26. Chalya PL, Mabula JB, Koy M, et al.  Typhoid intestinal perforations at a university teaching hospital in Northwestern Tanzania: a surgical experience of 104 cases in a resource-limited setting. World J Emerg Surg 2012; 7:4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27. Ugochukwu A, Amu O, Nzegwu M. Ileal perforation due to typhoid fever–review of operative management and outcome in an urban centre in Nigeria. Int J Surg 2013; 11:218–22. [DOI] [PubMed] [Google Scholar]
  • 28. Sheshe AA, Anyanwu L-JC, Mohammad AM, et al.  Typhoid intestinal perforation: analysis of the outcome of surgical treatment in Kano, Nigeria. Arch Med Health Sci 2018; 6:59. [Google Scholar]
  • 29. Sudarshan PB, Sundaravadanan BS. Analysis of enteric ileal perforation: a prospective study in a tertiary care hospital. Int Surg J 2017; 4:899–902. [Google Scholar]
  • 30. Agrawal P, Imbisat MZ. Our experience with enteric ileal perforation: a retrospective study at a tertiary care centre in northern India. Int Surg J 2019; 6:4318–22. [Google Scholar]
  • 31. Jhobta RS, Attri Ak, Kaushik R, et al.  Spectrum of perforation peritonitis in India: review of 504 consecutive cases. World J Emerg Surg 2006; 1:26. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32. Ansari AG, Naqvi SQ, Ghumro AA, Jamali AH, Talpur AA. Management of typhoid ileal perforation: a surgical experience of 44 cases. Gomal J Med Sci 2009; 7:26–30. [Google Scholar]
  • 33. Edino ST, Yakubu AA, Mohammed AZ, Abubakar IS. Prognostic factors in typhoid ileal perforation: a prospective study of 53 cases. J Natl Med Assoc 2007; 99:1042–5. [PMC free article] [PubMed] [Google Scholar]
  • 34. Beniwal US, Jindal D, Sharma J, Jain S. Comparative study of operative procedures in typhoid perforation. Indian J Surg 2003; 65:172–77. [Google Scholar]
  • 35. Grema BA, Aliyu I, Michael GC, et al.  Typhoid ileal perforation in a semi-urban tertiary health institution in North-Eastern Nigeria. S Afr Fam Pract 2018; 60:168–73. [Google Scholar]
  • 36. Mogasale V, Desai SN, Mogasale VV, Park JK, Ochiai RL, Wierzba TF. Case fatality rate and length of hospital stay among patients with typhoid intestinal perforation in developing countries: a systematic literature review. PLoS One 2014; 9:e93784. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37. Shrivastava D, Kumar JA, Pankaj J, Bala SD, Sewak VR. Typhoid intestinal perforation in Central India: a surgical experience of 155 cases in resource limited setting. IJBAR 2014; 5:600–4. [Google Scholar]
  • 38. Saxe JM, Cropsey R. Is operative management effective in treatment of perforated typhoid? Am J Surg 2005; 189:342–4. [DOI] [PubMed] [Google Scholar]
  • 39. Ukwenya A, Ahmed A, Garba E. Progress in management of typhoid perforation. Ann Afr Med 2011; 10:259–65. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

ciaa1309_suppl_Supplementary_Table_1

Articles from Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America are provided here courtesy of Oxford University Press

RESOURCES