Elsevier

Pancreatology

Volume 17, Issue 5, September–October 2017, Pages 669-674
Pancreatology

Early discharge in Mild Acute Pancreatitis. Is it possible? Observational prospective study in a tertiary-level hospital

https://doi.org/10.1016/j.pan.2017.07.193Get rights and content

Abstract

Background and aims

In acute pancreatitis (AP), first 24 h are crucial as this is the period in which the greatest amount of patients presents an organ failure. This suggests patients with Mild AP (MAP) could be early identified and discharged. This is an observational prospective trial with the aim to demonstrate the safety of early discharge in Mild Acute Pancreatitis (MAP).

Methods

Observational prospective study in a third level single centre. Consecutive patients with AP from March 2012 to March 2014 were collected. Inclusion criteria: MAP, tolerance to oral intake, control of pain, C Reactive Protein <150 mg/dL and blood ureic nitrogen < 5 mg/dL in two samples. Exclusion criteria: pregnant, lack of family support, active comorbidities, temperature and serum bilirubin elevation. Patients with MAP, who met the inclusion criteria, were discharged within the first 48 h. Readmissions within first week and first 30 days were recorded. Adverse effects related to readmissions were also collected.

Results

Three hundred and seventeen episodes were collected of whom 250 patients were diagnosed with MAP. From these, 105 were early discharged. Early discharged patients presented a 30-day readmission rate of 15.2% (16 patients out of 105) corresponding to the readmission rates in Acute Pancreatitis published to date. Any patient presented adverse effects related to readmissions.

Conclusion

Early discharge in accurately selected patients with MAP is feasible, safe and efficient and leads to a decrease in median stay with the ensuing savings per process and with no increase in readmissions or inmorbi-mortality.

Section snippets

Background and aims

Acute pancreatitis (AP) is a broad-ranging entity, which can go from a mild self-limiting disease that requires merely symptomatic treatment to a severe life-threatening illness that may require intensive care admission and aggressive treatment [1].

Our main objective in cases of AP is early detection of patients with severe condition or who are likely to worsen [2].

The first 24–48 h are crucial, as this is the period in which the highest proportion of patients present organ failure [3], [4].

Methods

This is a single-centre prospective observational study at a tertiary-level hospital. All consecutive adult patients (over 18 years old) diagnosed with AP and admitted to our centre from March 2012 to March 2014 were included. Diagnosis was based on characteristic abdominal pain, combined with elevated serum levels of pancreatic enzymes, as recommended in guidelines [1].

Data on demographic, clinical and laboratory parameters were recorded during the patient's admission to the emergency

Results

A total of 317 episodes were recorded between March 2012 and March 2014. Patients' mean age was 62 years (range: 18 to 96).

The flow chart in Fig. 2 presents the patients' distribution. One patient was excluded due to an error in the severity classification, and 66 patients who presented a moderate, severe or critical AP according to the DBC [5] were also excluded. From the 250 patients diagnosed with MAP within this period, 145 required admission for the reasons outlined in Table 1. Finally,

Discussion

This single-centre prospective observational study at a tertiary-level hospital was designed to assess the feasibility, safety and efficiency of a protocol for early discharge in selected patients diagnosed with MAP.

Patients without organ failure were classified as MAP by the Determinant Based Classification (DBC) [5] and by the Atlanta Modified Classification [6], which both have high potency for detecting more severe acute pancreatitis. In both classifications, the absence of organ failure

Disclosure

The authors have nothing to disclose.

Author's contributions

Neus Garcia Monforte involvement in the study was taking part in the design of the study.

Francisco Javier García Borobia involvement in the study was taking part in the design of the study.

Pere Rebasa Cladera involvement in the study was taking part in the design of the study and in the statistical analysis.

Juan Carlos García Pacheco involvement in the study was taking part in the acquisition of data.

Andreu Romaguera Monzonís involvement in the study was taking part in the acquisition of data.

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