On 22 March 2020, an eight-year-old female was referred to Shahid Beheshti hospital, Qom city, with weakness, lethargy, abdominal pain, nausea, and fever (sublingual temperature more than 38°C). She had had these symptoms for two days (from 19 March 2020). She did not have any medical history, specific risk factors, or background of receiving any drugs.
Upon admission to the hospital, she looked ill, and her vital signs were as follows: Blood pressure 85/60 mmHg; pulse rate 140 bpm; respiratory rate 58 bpm; and oral temperature 38.5°C. Laboratory assays were conducted to evaluate overall health and detect a disorder. A summary of the clinical outcomes is given in
Table 1. The serum levels of alanine transferase (ALT), aspartate amino transferase (AST), and alkaline phosphatase were in the normal range. Total protein and CRP-1h levels were in the normal range. Echocardiography (ECG) did not reveal any abnormalities (mild TR, good LV function, normal PAP). Following more evaluations, we found evidence of crackle auscultation, and decreased auscultation in the patient.
On the day of hospitalization, the patient presented with acute respiratory distress, tachycardia, and tachypnea without any cyanosis. Concerning the positive result of laboratory-confirmed COVID-19 pneumonia (based on conventional PCR assay and sequencing of PCR amplicons using a throat swab) and fever, for the accurate confirmation of COVID-19 infection, we performed a chest CT scan. The chest CT scan revealed bilateral lung involvement with pleural effusion. The reduction in saturation (up to 67%) caused the patient’s condition to worsen on the day of COVID-19 pneumonia diagnosis, and the patient was hospitalized in the intensive care unit (ICU) and connected to a high-flow ventilator. In the ICU, the medication started with vancomycin IV 240 mg (up to three doses), tamiflu 75 mg (three tablets), and azithromycin 60 mg. The chronology of events by the parents confirmed that their child had no close contact with a suspected or confirmed COVID-19 case in the close family. On the day of hospitalization, the patient's condition worsened, and the patient’s PT, PTT, and D-dimer increased (
Table 1). Eventually, all therapeutic care was unsuccessful, and the patient expired due to acute respiratory distress syndrome (ARDS).
| Tests | Results | Reference Range |
|---|
| 8-Year-Old Female (22 March 2020) |
| Blood biochemistry | | |
| BS, mg/dL | 85 | Up to 120 |
| Creatinine, mg/dL | 1.3 a | Children: 0.3 - 0.7 |
| Uric acid, mg/dL | 4.8 | Children: 2 - 5.5 |
| SGOT (AST), IU/L | 22 | Female < 31; Male < 37 |
| SGPT (ALT), IU/L | 13 | Female < 31; Male < 41 |
| CRP, mg/dL | 32.1 a | Quantitative < 6: Negative |
| Immunohematology | | |
| rRT-PCR | Positive | |
| Hematology | | |
| WBC, × 103/µL | 7 | 6 - 12 years: 4.5 - 13.5 |
| RBC, 106/µL | 4.56 | 6 - 12 years: 4.0 - 5.2 |
| Platelet, 103/µL | 210 | 150 - 450 |
| ESR 1h, mm/h | 17 a | Children: 3 - 13 |
| LDH, IU/L | 165 | 8 - 16 years: 120 - 293 |
| Gasometer data | | |
| pH | 7.3 | 7.2 - 7.6 |
| SO2, % | 67 b | 90 - 100 |
| Coagulation | | |
| Patient PT, sec | 27 a | 11 - 13.5 |
| INR | 2.5 | - |
| Control PT, sec | 13 | - |
| PTT, sec | 66 a | 25 - 45 |
| D-dimer, ng/mL | 12230 a | Up to 500 |
| 16-Month-Old Male (24 March 2020) |
| Blood biochemistry | | |
| BS, mg/dL | 93 | Up to 120 |
| Creatinine, mg/dL | 0.6 a | 0.2 - 0.4 |
| Urea, mg/dL | 13 | 11 - 36 |
| SGOT (AST), U/L | 35 | < 37 |
| SGPT (ALT), U/L | 31 | < 41 |
| CRP, mg/dL | 14.3 a | Up to 10 negative |
| Immunohematology | | |
| rRT-PCR | Positive | |
| Hematology | | |
| WBC, × 103/µL | 11.5 | 5 - 18.5 (for 1 - 16 months) |
| RBC, 106/µL | 4.42 | 2 - 5.9 (for 16 month infants) |
| Platelet, 103/µL | 309 | 150 - 450 |
| ESR 1h, mm/h | 7 a | 0 - 5 |
| LDH, IU/L | 292 | 170 - 490 |
| Gasometer data | | |
| pH | 7.1 | 7.2 - 7.6 |
| SO2, % | 58 b | 90 - 100 |
| PO2, mm Hg | 54 b | 80 - 100 |
| Coagulation | | |
| Patient PT, sec | 16.8 a | 11 - 13.5 |
| INR | 2.5 | - |
| Control PT, sec | 13 | - |
| PTT, sec | 63 a | 25 - 45 |
Abbreviations: BS, blood sugar; AST, aspartate amino transferase; ALT, alanine transferase; CRP, C-reactive protein; RT-PCR, reverse transcription polymerase chain reaction; WBC, white blood cell; RBC, red blood cell; ESR, erythrocyte sedimentation rate; LDH, lactate dehydrogenase; PT, prothrombin time; INR, international normalized ratio; PTT, partial thromboplastin time.
a Higher than the reference value.
b Lower than the reference value.
On 24 March 2020, a 16-month-old male was referred to the Emergency Department of Shahid Beheshti hospital, Qom city, complaining of laryngomalacia, microcephaly, cerebral palsy (CP), and breathing distress. His medical history indicated tracheotomy and hospitalization history, and he received levebel and phenobarbital.
Upon admission to the hospital, he looked ill, and his vital signs were as follows: Blood pressure 85/50 mmHg; pulse rate 140 bpm; respiratory rate 35 bpm; and oral temperature 37.2°C. To accurately evaluate the patient, laboratory tests were performed. The results are summarized in
Table 1. The serum levels of ALT, AST, and alkaline phosphatase were in the normal range. Echocardiography (ECG) did not indicate any abnormalities. Laboratory-confirmed COVID-19 pneumonia was assessed using SARS-CoV-2 conventional PCR assay and sequencing of PCR amplicons, which was reported to be positive. After performing a chest CT scan, we noticed bilateral lung involvement with pleural effusion. Due to the persistence of dyspnea and reduction of saturation (up to 58%), the patient was admitted to the ICU and connected to a high-flow ventilator. Medication with vancomycin BD 120 mg (up to three doses) and Kaletra PG 7.5 mg was started following the first symptoms of SARS-CoV-2 infection to reduce pneumonia and acute respiratory distress. The infant's condition worsened on the second day of hospitalization, and the patient’s PT, PTT, and INR increased (
Table 1). Eventually, on 4 April 2020, the patient was expired due to ARDS.