# Etiology, treatment outcome and prognostic factors among patients with secondary peritonitis at Bugando Medical Centre, Mwanza, Tanzania

**Authors:** Amri Mabewa, Jeremiah Seni, Phillipo L. Chalya, Stephen E. Mshana, Japhet M. Gilyoma

PMC · DOI: 10.1186/s13017-015-0042-5 · World Journal of Emergency Surgery : WJES · 2015-10-06

## TL;DR

This study identifies common causes and risk factors for death in patients with secondary peritonitis at a hospital in Tanzania.

## Contribution

The study is the first to comprehensively evaluate etiologies, treatment outcomes, and prognostic factors for secondary peritonitis at Bugando Medical Centre.

## Key findings

- Perforated appendicitis, peptic ulcer disease, ischemia, and typhoidal perforation were the most common causes of secondary peritonitis.
- Premorbid illness and postoperative complications were strongly associated with patient death.
- Only 3% of patients arrived within 24 hours of symptom onset, and 15.5% of patients died.

## Abstract

Secondary peritonitis due to perforation of the gastrointestinal tract is one of the most common surgical emergencies all over the world and is associated with significantly morbidity and mortality. Previous studies conducted at Bugando Medical Centre (BMC) were retrospective and each was focused on single etiology; therefore there was an obvious need to evaluate the etiologies, treatment outcome and their prognostic factors altogether.

This was a descriptive cross-sectional study involving patients with secondary peritonitis admitted at BMC from May 2014 to April 2015. Sociodemographic and clinical characteristics among consented patients were collected using questionnaires. Peritoneal aspirate, biopsy and blood were collected perioperatively and processed using standard operating procedures. Analysis was done using STATA version 11 software.

The study enrolled 97 patients with the female to male ratio of 1:1.8 and approximately 41.2 % (40/97) were in their third and fourth decades of life. Only 3 (3.09 %) patients arrived to the hospital within 24 hours of onset of illness, 26 (26.80 %) patients presented with shock and HIV seropositivity among all patients was 13.40 % (13/97). The common etiologies of secondary peritonitis were perforated appendicitis 23 (23.71 %), peptic ulcer disease 18 (18.56 %), ischemia 18 (18.56 %) and typhoidal perforation 15 (15.46 %). Of the 97 patients, 35 (36.08 %) had complications and 15 (15.46 %) died. Presence of premorbid illness and post-operative complication were found to be associated with death (p values = 0.004 and <0.001 respectively).

The most common etiologies of secondary peritonitis at BMC are perforated appendicitis, peptic ulcer disease, ischemia and typhoidal perforation. Premorbid illness and postoperative complications in this setting are associated with death and as the matter of fact proper screening on admission should be done to identify patients with premorbid illness and confer prompt management.

## Linked entities

- **Diseases:** peptic ulcer disease (MONDO:0004247)

## Full-text entities

- **Genes:** CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}
- **Diseases:** Typhoid (MESH:D014435), perforation of the gastrointestinal tract (MESH:D005770), Appendicitis (MESH:D001064), HIV (MESH:D015658), Trauma (MESH:D014947), perforation (MESH:D057112), Peritonitis (MESH:D010538), Hypertension (MESH:D006973), Mortality (MESH:D003643), anemia (MESH:D000740), Ischemia (MESH:D007511), Gastric (MESH:D013272), gastrointestinal perforation (MESH:D005767), Diarrhea (MESH:D003967), infection (MESH:D007239), AIDS (MESH:D000163), HIV seropositive (MESH:D006679), enterocutaneous (MESH:D007412), Fever (MESH:D005334), postoperative complications (MESH:D011183), portal hypertension (MESH:D006975), Abdominal pain (MESH:D015746), Constipation (MESH:D003248), gall bladder (MESH:D005706), rigidity (MESH:D009127), bacterial (MESH:D001424), Septicemia (MESH:D018805), complication (MESH:D008107), abscess (MESH:D000038), Neoplastic (MESH:D009369), Dehydration (MESH:D003681), Vomiting (MESH:D014839), Heart failure (MESH:D006333), multisystem organ failure (MESH:D009102), fistula (MESH:D005402), shock (MESH:D012769), tenderness (MESH:D063806), Pneumoperitoneum (MESH:D011027), Puerperal sepsis (MESH:D011644), ascites (MESH:D001201), peptic ulcer (MESH:D010437), Wound dehiscence (MESH:D013529), volvulus (MESH:D045822), inflammatory (MESH:D007249), febrile (MESH:D000071072), Salmonella infection (MESH:D012480), Renal failure (MESH:D051437)
- **Species:** Helicobacter pylori (species) [taxon 210], Human immunodeficiency virus 1 (no rank) [taxon 11676], Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC4595331/full.md

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Source: https://tomesphere.com/paper/PMC4595331