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BMJ Case Rep: first published as 10.1136/bcr-2021-243908 on 5 July 2021. Downloaded from http://casereports.bmj.com/ on July 6, 2021 at AIIMS Rishikesh. Protected by copyright.
Ventilator-associated pneumonia due to carbapenem-
resistant Providencia rettgeri
Nupur B Patel , Gaurav Jain, Saurabh Chandrakar , Beeraling Ningappa Walikar
Department of Anesthesia and SUMMARY An abdominal X-ray was done, which showed air
Critical Care, AIIMS Rishikesh, Ventilator-associated pneumonia (VAP) is one of the under the diaphragm with dilated bowels. A diag-
Rishikesh, India leading cause of mortality and morbidity in critically ill nosis of hollow viscous perforation was made and he
patients on mechanical ventilation. We report a case of was immediately taken for emergency laparotomy.
Correspondence to He was intubated using rapid sequence induction
VAP caused by Providencia rettgeri in a postoperative
Dr Nupur B Patel;
nupurbpatel@yahoo.co.in 58-year-old man with prepyloric perforation. The with continuous cricoid pressure to prevent aspi-
patient’s ICU stay was complicated by VAP. As the ration. He had prepyloric perforation, which was
Accepted 10 June 2021 organism was carbapenem resistant, high-dose extended repaired by an omental patch. During the surgery,
infusion of meropenem along with cefepime was started. patient developed hypotension for which fluid
Early identification and treatment helped in successful boluses were given and low-dose norepinephrine
weaning of the patient from the ventilator. Providencia was started. Arterial blood gas (ABG) was suggestive
is an emerging nosocomial pathogen with an increase of metabolic acidosis. Postoperatively, he was trans-
in resistance pattern. This case highlights the rarity and ferred to the intensive care unit (ICU) in view of
importance of Providencia as a cause of VAP. septic shock. On arrival to the ICU, he had a heart
rate of 112 beats/min, blood pressure of 132/76 mm
Hg with norepinephrine 20 μg/min and saturation
of 98% with endotracheal tube in situ. He was put
BACKGROUND
on invasive mechanical ventilator synchronised
Ventilator-associated pneumonia (VAP) is defined
intermittent mandatory ventilation mode with tidal
as pneumonia that occurs 48 hours or more after
volume of 400 mL, pressure support (PS) of 12 cm
endotracheal intubation. The incidence of VAP
H2O, PEEP (Positive end expiratory pressure) of
is 9%–27% with a mortality rate of 9%–13%.1
6 cm H2O, respiratory rate of 18 breaths/min and
Common pathogens known to cause VAP are Pseu-
fractional inspired oxygen (FiO2) of 40%.
domonas (24.4%), Staphylococcus aureus (20.4%),
Enterobacteriaceae (14.1% includes Klebsiella spp,
Escherichia coli, Proteus spp, Enterobacter spp, INVESTIGATIONS
Serratia spp and Citrobacter spp), Streptococcus sp In the ICU baseline ABG, chest X-ray and routine
(12.1%), Haemophilus sp (9.8%), Acinetobacter blood investigations were done (table 1). ABG
sp (7.9%), Neisseria sp (2.6%), Stenotrophomonas showed metabolic acidosis with a pH of 7.21,
maltophilia (1.7%), coagulase- negative Staphy- partial pressure of oxygen of 112 mmHg, partial
lococcus (1.4%), others (4.7% includes Coryne- pressure of carbon dioxide of 30 mmHg, bicar-
bacterium, Moraxella, Enterococcus and fungi).1 bonate of 15 mEq and base deficit of −12 mEq.
Providencia rettgeri, a gram negative bacillus, is a Initial chest X-
ray (figure 1A) was normal. He
rare cause of VAP. To the best of our knowledge, was empirically started on injection (intravenous)
this is the first reported case of VAP in India due to ceftriaxone 1 g two times per day and metronida-
carbapenem-resistant P. rettgeri. zole 500 mg three times per day after taking blood
cultures. Fluid boluses were administered as he
was fluid responsive. Gradually, he was tapered off
CASE PRESENTATION the vasopressors on postoperative day 2 and was
A 58- year-
old man presented to the emergency planned for weaning. The next day, he developed
department with abdominal pain and vomiting fever (101 F), tachypnoea (28 breaths/min) and
for 3 days. The pain was sudden in onset, initially tachycardia (132 breaths/min) with an increase in
localised to the umbilicus and then spread to the ventilatory requirements (FiO2: 60%, PS: 15 cm
entire abdomen. He had received analgesic (tablet
paracetamol) and antiemetic (tablet ondansetron)
from a primary care physician. But his symptoms
were not relieved and for the past 24 hours, he had
severe abdominal distension with non-passage of
© BMJ Publishing Group
Limited 2021. No commercial stool or flatus for which he came to the hospital.
re-use. See rights and He did not have any previous surgical history or
permissions. Published by BMJ. any comorbidities. On examination, he was dehy-
drated, tachycardic (122 breaths/min) and tachy-
To cite: Patel NB, Jain G,
Chandrakar S, et al. BMJ pnoeic (34 breaths/min). Abdomen was distended
Case Rep 2021;14:e243908. with generalised and rebound tenderness. Guarding
doi:10.1136/bcr-2021- and rigidity were present and bowel sounds were Figure 1 Chest X-ray on intensive care unit admission
243908 diminished. (A) and on postoperative day 3 (1B).
Patel NB, et al. BMJ Case Rep 2021;14:e243908. doi:10.1136/bcr-2021-243908 1
Case report
BMJ Case Rep: first published as 10.1136/bcr-2021-243908 on 5 July 2021. Downloaded from http://casereports.bmj.com/ on July 6, 2021 at AIIMS Rishikesh. Protected by copyright.
Table 1 Laboratory data at admission and during hospitalisation
Postoperative day 3
Variable ICU admission (VAP onset) Day 5 Day 7 Day 10 Day 12
Haemoglobin (g/dL) 10.6 8.7 9 10.8 899 10.1
White cell count (×109/L) 7000 16 600 17 200 9080 8520 6400
Platelets (/μL) 250 000 170 000 267 900 396 000 288 000 286 000
Neutrophils (%) 74 88 84 72 68 71
Creatinine (mg/dL) 1.2 1.4 1.42 0.88 1.1 0.92
Procalcitonin (mg/L) 2 15 3
ICU, intensive care unit; VAP, ventilator-associated pneumonia.
H2O and PEEP: 10 cm H2O). He had purulent endotracheal Blood, urine and tracheal cultures were taken. Antibiotic was
secretions. Repeat chest X-ray was done on postoperative day 3, broadened to intravenous meropenem 1 g three times per day.
which showed right lower zone consolidation (figure 1B). Blood Tracheal culture revealed 1 000 000 CFU/mL non-haemolytic
investigations showed an increase in white blood cell count with gram-negative bacilli. The organism was a non-lactose fermenter,
elevated procalcitonin (table 1). A diagnosis of VAP was made. positive for mannitol, citrate, urease, rhamnose and inositol, and
BMJ Case Rep: first published as 10.1136/bcr-2021-243908 on 5 July 2021. Downloaded from http://casereports.bmj.com/ on July 6, 2021 at AIIMS Rishikesh. Protected by copyright.
negative for sucrose. It was identified as P. rettgeri by VITEK 2 Providencia is not commonly found in tracheal aspirates but,
automated system. when it is, it is usually deemed to be colonisation (ie, not a
source of infection). But in our patient, the colony-forming unit
TREATMENT count and sensitivity pattern were in favour of its pathogenicity.
As the organism was carbapenem resistant (figure 2), high-dose Also, there was clinical and radiological improvement after anti-
extended infusion of meropenem (2 g) over 3 hours three times biotics were broadened and the patient was gradually weaned
per day was given along with high-dose intravenous cefepime off the ventilator.
2 g three times per day. Urine and blood cultures did not reveal Providencia sp are generally resistant to polymyxin, tetra-
any bacterial growth. Gradually, the patient was weaned off the cyclines, older generation cephalosporins and ampicillin but
ventilator on postoperative day 10. He was shifted to the surgery susceptible to newer cephalosporins, imipenem, meropenem
ward on postoperative day 12. and aztreonam. They have variable susceptibilities to aminogly-
cosides, trimethoprim–sulfamethoxazole and fluoroquinolones.6
In our case, the organism was carbapenem resistant, so we had
OUTCOME AND FOLLOW-UP limited antibiotic options. High-dose extended meropenem infu-
Antibiotics were continued for a total duration of 14 days. sion was proven effective against some enterobacteria.7 Hence,
He was discharged on postoperative day 16 and was asked to we decided to start high-dose extended meropenem infusion
follow-up in surgery outpatient clinics after 1 month. along with high-dose cefepime for our patient.
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