Management of Recurrent Clostridioides difficile Infection in a Frail Elderly Patient with Multiple Comorbidities
For this 79-year-old patient completing fidaxomicin therapy for her second episode of CDI, the priority is preventing a third recurrence through extended prophylaxis with oral vancomycin tapered-pulsed regimen, aggressive management of her multiple recurrence risk factors (age, CKD, CHF, PPI use, hypoalbuminemia), and consideration of fecal microbiota transplantation if she experiences another recurrence. 1
Immediate CDI Management (Current Episode)
Complete the current fidaxomicin course as ordered (through 11/13/25), as she is clinically responding with resolution of diarrhea and no systemic symptoms. 1
Continue cholestyramine through 11/15/25 as ordered, though evidence for its efficacy in preventing recurrence is limited; it may bind residual toxins but should not interfere with ongoing fidaxomicin absorption given the timing. 1
Continue Lactobacillus supplementation, recognizing that while Saccharomyces boulardii and Lactobacillus species show promise for CDI recurrence prevention, none has demonstrated significant and reproducible efficacy in controlled trials. 1
Maintain strict contact/droplet isolation precautions with single-room isolation; reinforce handwashing with soap and water (not alcohol-based sanitizers, which do not inactivate C. difficile spores) for all staff and visitors. 2
Prevention of Third Recurrence (Critical Priority)
This patient is at extremely high risk for a third recurrence based on multiple factors: age >65 years, second recurrence, CKD stage 3, CHF, continued PPI use, hypoalbuminemia (albumin 3.9 g/dL is borderline), and frailty. 1, 3
Antibiotic Strategy After Fidaxomicin Completion
Initiate oral vancomycin tapered and pulsed regimen immediately after completing fidaxomicin (starting 11/14/25), as this is the IDSA/SHEA guideline-recommended approach for second or subsequent CDI recurrences. 1
Specific vancomycin taper-pulse regimen: Vancomycin 125 mg four times daily for 10–14 days, then 125 mg twice daily for 7 days, then 125 mg once daily for 7 days, then 125 mg every 2–3 days for 2–8 weeks. 1
Rationale: This extended regimen keeps C. difficile vegetative forms suppressed while allowing restoration of normal gut microbiota; fidaxomicin alone has shown less efficacy in patients with ≥2 recurrences. 1
Alternative consideration: Vancomycin standard course followed by rifaximin 400 mg three times daily for 20 days showed trend toward reduced recurrence (15% vs 31%, P=0.11 in small RCT), though evidence is weaker than for tapered-pulse vancomycin. 1
Addressing Modifiable Risk Factors
Discontinue or minimize PPI therapy (currently on omeprazole), as continued PPI use is associated with increased CDI recurrence risk; consider step-down to H2-blocker or PRN antacid therapy if GERD symptoms are minimal. 1
- Reassess PPI necessity given her current lack of reflux symptoms and the known association between PPIs and recurrent CDI. 1
Optimize nutritional status and albumin levels, as hypoalbuminemia is associated with worse CDI outcomes and recurrence. 1
Continue aggressive nutritional supplementation (Pro-Stat 30 mL BID, Ensure before meals, house supplement at bedtime) to maintain albumin >3.5 g/dL and prealbumin >20 mg/dL. 1
Consider albumin supplementation if levels drop below 2 g/dL, both for supportive care and potential anti-toxin properties. 1
Avoid all non-essential antibiotics during and after CDI treatment, as antibiotic exposure is the strongest risk factor for CDI recurrence. 1
If systemic antibiotics become necessary (e.g., for UTI, pneumonia), consider concurrent low-dose vancomycin prophylaxis (125 mg once daily) during and for 1 week after the antibiotic course, particularly given her history of multiple recurrences. 1
Two retrospective studies showed decreased risk of subsequent CDI in patients with prior recurrent CDI who received empiric vancomycin during subsequent antibiotic exposure, though prospective data are lacking. 1
Plan for Potential Third Recurrence
If she develops a third recurrence despite tapered-pulse vancomycin, strongly recommend fecal microbiota transplantation (FMT), which has strong evidence (moderate quality) for patients with multiple recurrences who have failed appropriate antibiotic treatments. 1
FMT efficacy: Success rates of 80–100% when administered via colonoscopy, with the first randomized trial showing marked superiority over vancomycin alone (cure rate 81% vs 31%, P<0.001). 1
FDA-approved oral FMT option (Vowst) is now available as prophylactic therapy for recurrent CDI, though cost and insurance coverage may be barriers. 4
Coordinate with gastroenterology/infectious diseases for FMT planning if third recurrence occurs. 1
Management of Comorbidities Affecting CDI Risk
Chronic Kidney Disease Stage 3
CKD increases both CDI risk and recurrence rates, with patients having higher mortality and healthcare costs. 3
Current renal function (Cr 1.33 mg/dL, eGFR 40 mL/min/1.73m²) is stable; continue weekly BMP monitoring as ordered. 3
Vancomycin dosing does not require adjustment for oral administration in CDI, as systemic absorption is minimal (<5%) and the drug acts locally in the GI tract. 1
Avoid nephrotoxic agents and NSAIDs; ensure adequate hydration to prevent prerenal azotemia (current BUN/Cr ratio of 24 suggests mild prerenal component). 3
Congestive Heart Failure
Maintain euvolemic state to optimize gut perfusion and immune function; current exam shows no edema and lungs are clear. 1
Continue furosemide Mon/Thu schedule with close monitoring of weights (weekly as ordered); adjust diuretics if volume status changes. 1
Low-normal BP (104/57 today) may reflect overdiuresis or medication effect; monitor for orthostatic hypotension and consider holding chlorthalidone if SBP persistently <100 mmHg. 1
Hypothyroidism with Elevated TSH
Markedly elevated TSH (19.19 µIU/mL) indicates under-replacement, which may contribute to constipation, fatigue, and impaired immune function. 2
Increase levothyroxine dose in consultation with PCP/endocrinology; typical adjustment is 12.5–25 mcg increase given age and cardiac history. 2
Ensure proper levothyroxine administration on empty stomach, separated by ≥4 hours from calcium, iron, and multivitamins to optimize absorption. 2
Recheck TSH in 6–8 weeks after dose adjustment. 2
Hyponatremia
Mild hyponatremia (Na 132 mmol/L) may worsen with aggressive diuresis or SIADH from multiple medications. 2
Monitor sodium with weekly CMPs as ordered; consider earlier recheck if mental status changes or weakness worsens. 2
Review diuretic regimen (chlorthalidone and furosemide) and consider reducing or holding chlorthalidone if sodium trends downward or BP remains low. 2
Ensure adequate oral solute intake (protein, sodium in diet) and avoid hypotonic fluids. 2
Monitoring and Follow-Up
Strict monitoring for CDI recurrence is essential given her high-risk profile. 1, 2
Nursing to document stool frequency and consistency each shift; notify provider immediately if ≥3 loose stools in 24 hours or any systemic symptoms (fever, abdominal pain, leukocytosis). 1, 2
Do not perform "test of cure" after CDI treatment, as testing cannot distinguish colonization from active infection. 1
Weekly labs (CBC, CMP, Mg, Phos) as ordered through 11/19/25 to monitor renal function, electrolytes, and WBC count. 2
Continue PT/OT/ST 5x/week and 4x/week respectively to address debility and reduce fall risk, which is critical for maintaining independence and quality of life. 2
Infection Control and Isolation
Maintain single-room isolation with contact/droplet precautions until facility criteria for discontinuation are met (typically 48 hours after diarrhea resolution, though policies vary). 2
Reinforce gown/glove use and handwashing with soap and water (not alcohol) for all staff and visitors entering room. 2
Environmental cleaning with sporicidal agents (bleach-based) is essential to prevent transmission. 2
Medication Reconciliation for CDI Risk
Review all medications for CDI risk factors and anticholinergic burden:
Oxybutynin ER: High anticholinergic burden may worsen cognition and constipation; consider discontinuation or switch to mirabegron if overactive bladder symptoms recur, as she is currently continent. 2
Clonazepam: High fall and cognitive risk in elderly; consider gradual taper with psychiatry input if anxiety is controlled, given her pleasant mood and good sleep. 2
Escitalopram: May contribute to hyponatremia; monitor sodium closely but continue if mood stable. 2
Goals of Care Alignment
DNR status is documented; ensure ongoing communication with patient/family about goals of care, particularly if third recurrence occurs or if FMT is being considered. 2
- Quality of life focus: Preventing recurrent CDI is critical to maintaining her functional status, avoiding rehospitalization, and supporting her ability to participate in rehabilitation. 2