Abstract
Background
Peritoneal dialysis (PD) is a commonly used form of renal replacement therapy for patients that have reached end-stage renal disease. Acute bacterial peritonitis (ABP) in chronic PD patients results in pain, increased costs, injury to the peritoneal membrane, and PD modality failure. Optimal antibiotic treatment of acute bacterial peritonitis (ABP) in chronic PD patients should be intraperitoneal, outpatient-based, appropriate, prompt, and uninterrupted. We investigated the frequency of and predisposition to suboptimal antibiotic courses for ABP in our chronic PD patients.
Methods
Twenty-four charts of patients with ABP were reviewed, to test the null hypothesis that all ABP patients received antibiotics optimally.
Results
After 12 patient exclusions (hospitalization), 9 suboptimal antibiotic events were detected in 6 of the remaining 12 patients, disproving the null hypothesis ( p < 0.02). Most suboptimal antibiotics courses (7 of 9) resulted from delays and/or gaps in therapy or antibiotics prescribed outside of community standard. Suboptimal antibiotic events occurred on nights and weekends rather than during the workweek ( p < 0.02) and in the emergency room rather than the PD clinic ( p < 0.02).
Conclusions
Suboptimal ABP antibiotic therapy occurs commonly and is influenced by time and location of presentation and lack of knowledge by patients and physicians. Prevention of suboptimal antibiotic courses in the treatment of ABP in chronic PD patients includes education of patients and providers and allowing emergency rooms and PD clinics to dispense antibiotics for home use.
Introduction
Peritoneal dialysis (PD) is an effective home-based renal replacement modality for patients with end stage kidney disease. The peritoneal lining functions as the semipermeable membrane for dialysis, once PD fluid is instilled into the peritoneal space via an indwelling catheter. PD is the dialysis modality for approximately 11% of the global dialysis population. Acute bacterial peritonitis (ABP) is a common complication of PD, usually presenting with cloudy PD effluent and abdominal pain. Although ABP episodes rarely result in death, severe or prolonged infection may cause peritoneal membrane failure and in fact is the main reason for change in dialysis modality from PD to in-center hemodialysis.
Best practice guidelines recommend intraperitoneal as the preferred route of antibiotics for the treatment of ABP. Unless features of sepsis or intractable pain are present, ABP should be treated on an outpatient basis. Once a sample of dialysis effluent has been collected in the peritoneal dialysis clinic (PDC) or the emergency room (ER) and sent for analysis, intraperitoneal antibiotics should be administered without delay, with daily antibiotic therapy to continue for 14–21 days, depending upon the organism cultured.
Unfortunately, there are barriers to expeditious diagnosis and treatment of ABP. Diagnosis may be delayed and/or inaccurate if patients do not realize that they have acquired ABP or if they live far from their PDC or an ER. We are particularly interested in barriers to prompt and continuous outpatient treatment of ABP, once PD fluid analysis and clinical evaluation have suggested the diagnosis of ABP. In our local health care system, we have observed a number of episodes of suboptimal outpatient intraperitoneal antibiotic treatment, after patients have presented with cloudy PD fluid and abdominal pain to a PDC or ER. However, it is unclear how common these episodes are and what clinical factors predispose to them. Clinical relevance is high, in that delayed, discontinuous, or inappropriate intraperitoneal antibiotic therapy predisposes to prolonged pain, increased risk of bacteremia, sepsis, death, prolonged peritoneal inflammation, scarring of the peritoneal membrane, PD modality failure, and excessive medical costs.
To determine the frequency of chronic PD patients not receiving appropriate outpatient intraperitoneal antibiotics for ABP promptly and consistently, as well as to assess the risk factors for these inconsistencies, we reviewed all cases of ABP from a single PDC over a 17-month period. We tested the null hypothesis that all chronic PD patients with ABP received appropriate outpatient intraperitoneal antibiotics promptly upon presentation to the PDC or ER with subsequent continuous (ie daily) therapy on an outpatient basis, without gaps in therapy for the entire prescribed length of therapy. To our knowledge, this type of analysis has not been performed previously.
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