LETTER TO EDITOR |
https://doi.org/10.5005/jp-journals-10071-23728 |
Acute Flaccid Quadriparesis in a Recovering COVID-19 Patient: A Clinical Dilemma
1–4Department of Critical Care Medicine, Sir Ganga Ram Hospital, New Delhi, India
Corresponding Author: Sangeeta Chakraborty, Department of Critical Care Medicine, Sir Ganga Ram Hospital, New Delhi, India, Phone: +91 9830356827, e-mail: brightsky@rediffmail.com
How to cite this article Sabharwal P, Chakraborty S, Tyagi N, Kumar A. Acute Flaccid Quadriparesis in a Recovering COVID-19 Patient: A Clinical Dilemma. Indian J Crit Care Med 2021;25(2):238–239.
Source of support: Nil
Conflict of interest: None
Keywords: COVID-19, Guillain-Barré syndrome, Quadriparesis
A 39-year-old woman developed progressive breathing difficulty on July 7 which on evaluation at a private hospital was tested positive for COVID-19 RT PCR. After one day of stay, the patient came to our hospital on a non-rebreathing mask. The increasing oxygen requirement led to intubation and mechanical ventilation on the second day of admission. Patient was managed with intravenous cefuroxime sulbactam 1.5 gm BD, methylprednisone 60 mg BD for five days which was tapered over the next 4 days, inj Remdesivir 200 mg for the first day followed by 100 mg OD next 4 days, and thromboprophylaxis in the form of dalteparin 5000 subcutaneously BD. On the very next day after intubation patient was prone in view of the low PaO2/FiO2 ratio. After three proning sessions patient was finally extubated on July 19. On the third day post extubation, the patient was on room air and ward shifting was planned when the patient complaint of tingling sensation along with weakness in the lower limbs which progressed and involved the upper limb the next day. The neurologic examination revealed severe (medical Research council grade 2/5) distal symmetrical upper and lower limb weakness, loss of deep tendon reflexes, preserved pinprick, and light touch sensation. On the fifth day of post-extubation, an MRI brain and spine were done to rule out any nerve compression, which was normal. Also, a nerve conduction study was done. Neurophysiologic findings were suggestive of acute motor-sensory axonal neuropathy suggesting a clinical diagnosis of Guillain-Barré syndrome (GBS) (Table 1),1 although the possibility of peripheral neuropathy secondary to any drug or critical illness itself could not be ruled out. However, the consent for lumbar puncture was not given by the patient hence could not be done initially. Clinically, the patient maintained oxygenation on nasal prongs 4–6 L/min flow and the oxygen requirement did not increase further. Based on clinical suspicion and NCV finding patient was started on intravenous immunoglobulin infusion 2 gm/kg for 5 days. Patient’s weakness started improving gradually and by the third day of IVIg therapy, the patient came on room air with some residual paresis in lower limbs. After three days of IVIg, therapy patient agreed to undergo a lumbar puncture. In pursuit of establishing the diagnosis, a lumbar puncture and CSF study was done, which came out to be negative for albuminocytological dissociation. IVIg was discontinued after three days because of lack of evidence. Patient continued to improve gradually and was discharged after 22 days of hospital stay.
Neuromuscular weakness amounting to flaccid quadriparesis in recovering patients in ICU is fairly common. Some common causes possible for ICU-acquired weakness (ICUAW) in this patient could be (1) critical illness neuropathy (CIN), (2) drug-induced peripheral neuropathy, (3) steroid-induced myopathy, (4) neuromuscular blockade (NMB) related muscle weakness, (5) prone position leading to spinal nerve root compression, (6) dyselectrolytemia, and (7) GBS.2 After ruling out the possibility of causes (3)–(5) by MRI and NCV and ruling out dyselectrolytemia and any drug causing peripheral neuropathy clinical dilemma persisted between causes (1) and (7). Cases of GBS have been reported in patients infected with SARS-CoV-2 after 10–15 days of symptom onset.3,4 Typically, our patient presented with this weakness, 14 days after the symptom onset with a characteristic distal symmetrical pattern and a characteristic NCV which leaned our diagnosis towards GBS. Improvement after initiation of IVIg substantiated the clinical diagnosis further. CIN is also fairly common in ICU after the first two weeks of turbulent clinical course. Considering the fact that CIN commonly manifests as weaning failure, the clinical manifestation here was unclear,5 but having an axonal neuropathy with absent albuminocytological dissociation leaves us with a conclusion of probable diagnosis of CIN masquerading as GBS.
Nerve conduction | Distal latency (ms) | Amplitude (mV) | Conduction velocity (ms−1) | Area mV×ms |
---|---|---|---|---|
Motor | ||||
Right median | ||||
Wrist | 2.5 | 4.4 | 17.3 | |
Elbow | 6.5 | 4.2 | 55.8 | 15 |
Arm | 7.7 | 3.7 | 49.9 | 10.5 |
R ulnar | ||||
Wrist | 3.1 | 4.0 | 14.6 | |
Elbow | 6.4 | 3.7 | 64.2 | 14.0 |
Arm | 7.6 | 3.6 | 60.6 | 13.2 |
R peroneal | ||||
Sole of the foot | 2.2 | 1.3 | 8.7 | |
Head of the fibula | 11.8 | 1.4 | 9.3 | |
Popliteal fossa | 12.8 | 1.3 | 7.5 | |
L peroneal | ||||
Sole of the foot | 6.6 | 0.3 | 1.5 | |
Head of the fibula | 12.5 | 0.3 | 46.4 | 1.7 |
Popliteal fossa | 13.9 | 0.4 | 50.2 | 2.6 |
R tibial | ||||
Medial malleolus | 6 | 3.1 | 8.9 | |
Popliteal fossa | 12.7 | 3.3 | 57.2 | 14.5 |
L tibial | ||||
Medial malleolus | 8.4 | 4.2 | 19.9 | |
Popliteal fossa | 17 | 4.3 | 44.3 | 23.1 |
Sensory | ||||
R median | ||||
Digit | 2.1 | 15.4 | 56.1 | 10.2 |
Midpalm | 1.4 | 49.1 | 44.1 | 45.7 |
R ulnar | ||||
Digit | 1.9 | 19.9 | 26.8 | |
Midpalm | 1.0 | 3.2 | 1.6 |
ORCID
Pranshuta Sabharwal https://0000-0003-3914-5867
Sangeeta Chakraborty https://orcid.org/0000-0003-1331-1572
Niraj Tyagi https://0000-0001-5862-9731
Amber Kumar https://0000-0003-3411-5917
REFERENCES
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