Re: Clinical characteristics of 113 deceased patients with coronavirus disease 2019: retrospective study
Dear Editor
This is an interesting article from a Paediatric Surgeon’s perspective.
We would like to highlight the possibility of histopathology similarity between the critically ill SARS-Cov-2 patients to moribund infants with a congenital diaphragmatic hernia (CDH). Hopefully, this may lead to a possible lead upon clinical management of the acutely ill SARS-CoV-2 patients.
A) CLINICAL COURSE SIMILARITY:
The novel coronavirus disease 2019 (COVID-19) can induce acute respiratory distress syndrome (ARDS), which can progress to refractory pulmonary failure. The mortality of critically ill patients with SARS-CoV-2 pneumonia is considerable. The survival time of the non-survivors is likely to be within 1–2 weeks after ICU admission. [1] In such cases, extracorporeal membrane oxygenation (ECMO) may be considered as rescue therapy.
Similarly, in the immediate postnatal phase of some CDH moribund infants, there is a short period of better oxygenation referred to as the “honeymoon” period. [2] However, progressive deterioration in oxygenation is commonly observed due to a combination of pulmonary arterial hypertension, right ventricular hypertrophy and/or failure, and left ventricular hypoplasia with pulmonary venous hypertension results in severe Persistent pulmonary hypertension of the newborn (PPHN) unresponsive to conventional management following birth. [2]
Treatment after birth requires all the refinements of critical care including extracorporeal membrane oxygenation (ECMO) prior to surgical correction.
B) HISTOPATHOLOGIC SIMILARITY:
Animal models of CDH have demonstrated that in utero compression of developing fetal lungs by herniated abdominal viscera impairs pulmonary growth and maturation, resulting in pulmonary hypoplasia, which can be quantified by histologic, biochemical, and pulmonary morphometric techniques. Whatever its cause, pulmonary hypoplasia, which usually is a bilateral process, even in unilateral CDH, results in alveolar hypoplasia and a distinctly abnormal pulmonary vascular bed. Arterial branches are reduced, and there is a medial thickening in the small preacinar and intra-acinar arterioles. The physiologic consequence of this abnormality in pulmonary vasculature is an increase in pulmonary vascular resistance, which contributes to the development of persistent pulmonary hypertension, arguably the principal determinant of mortality in CDH. Another contributing factor appears to be a hyperreactivity to known stimuli of pulmonary vasoconstriction, including hypoxia, acidosis, hypothermia, and stress.
Similarly, the microscopic findings in SARS-CoV-2 patients included diffuse alveolar damage with exudates. The inflammation was predominantly lymphocytic, and multinucleated giant cells were seen alongside large atypical pneumocytes, although no definitive viral inclusions were noted.
POSSIBLE INFERENCES:
ECMO IN CDH moribund Infants provides a means of maintaining oxygen delivery only temporarily, and its salvage rate depends on the reversibility of the pathologic factors that led to respiratory failure within the time frame that ECMO can be used. Although the pulmonary hypoplasia associated with CDH can be “outgrown”, the time required for this adaptive process often exceeds that provided by ECMO bypass. This accounts for the significant differences in survival observed between patients who have CDH and those who have more rapidly reversible causes of respiratory failure, including PPHN, meconium aspiration syndrome, and sepsis.
However, that may not be the case in critically ill SARS-CoV-2. Hopefully, the timely use of ECMO would lead to better clinical outcomes in critically ill SARS-CoV-2 patients as compared to CDH infants. More so considering that in the study of ECMO for ARDS in patients with Middle East Respiratory Syndrome Coronavirus (MERS-CoV), a similar coronavirus disease that emerged in 2012, a significant decrease of in-hospital mortality rate and length of intensive care unit (ICU) stay was found in patients treated with ECMO compared to those managed with conventional therapy.
References:
1. Brandon Michael Henry, Giuseppe Lippi. Poor survival with extracorporeal membrane oxygenation in acute respiratory distress syndrome (ARDS) due to coronavirus disease 2019 (COVID-19): Pooled analysis of early reports. J. Crit Care 2020 Apr 1 doi: 10.1016/j.jcrc.2020.03.011 [Epub ahead of print]
2. Nair J, Lakshminrusimha S. Update on PPHN: mechanisms and treatment. Semin Perinatol. 2014;38(2):78–91.
Competing interests:
No competing interests
16 April 2020
Jahoorahmad Patankar
General Pediatric Surgeon
Dr Hemant Lahoti (MCh. - Paediatric Surgeon & Associate professor, Dept of Pediatric Surgery, D Y Patil Medical College, Navi Mumbai. D Y Patil hospital, Sector 5, Nerul, Navi Mumbai. Maharashtra 400706)
Rapid Response:
Re: Clinical characteristics of 113 deceased patients with coronavirus disease 2019: retrospective study
Dear Editor
This is an interesting article from a Paediatric Surgeon’s perspective.
We would like to highlight the possibility of histopathology similarity between the critically ill SARS-Cov-2 patients to moribund infants with a congenital diaphragmatic hernia (CDH). Hopefully, this may lead to a possible lead upon clinical management of the acutely ill SARS-CoV-2 patients.
A) CLINICAL COURSE SIMILARITY:
The novel coronavirus disease 2019 (COVID-19) can induce acute respiratory distress syndrome (ARDS), which can progress to refractory pulmonary failure. The mortality of critically ill patients with SARS-CoV-2 pneumonia is considerable. The survival time of the non-survivors is likely to be within 1–2 weeks after ICU admission. [1] In such cases, extracorporeal membrane oxygenation (ECMO) may be considered as rescue therapy.
Similarly, in the immediate postnatal phase of some CDH moribund infants, there is a short period of better oxygenation referred to as the “honeymoon” period. [2] However, progressive deterioration in oxygenation is commonly observed due to a combination of pulmonary arterial hypertension, right ventricular hypertrophy and/or failure, and left ventricular hypoplasia with pulmonary venous hypertension results in severe Persistent pulmonary hypertension of the newborn (PPHN) unresponsive to conventional management following birth. [2]
Treatment after birth requires all the refinements of critical care including extracorporeal membrane oxygenation (ECMO) prior to surgical correction.
B) HISTOPATHOLOGIC SIMILARITY:
Animal models of CDH have demonstrated that in utero compression of developing fetal lungs by herniated abdominal viscera impairs pulmonary growth and maturation, resulting in pulmonary hypoplasia, which can be quantified by histologic, biochemical, and pulmonary morphometric techniques. Whatever its cause, pulmonary hypoplasia, which usually is a bilateral process, even in unilateral CDH, results in alveolar hypoplasia and a distinctly abnormal pulmonary vascular bed. Arterial branches are reduced, and there is a medial thickening in the small preacinar and intra-acinar arterioles. The physiologic consequence of this abnormality in pulmonary vasculature is an increase in pulmonary vascular resistance, which contributes to the development of persistent pulmonary hypertension, arguably the principal determinant of mortality in CDH. Another contributing factor appears to be a hyperreactivity to known stimuli of pulmonary vasoconstriction, including hypoxia, acidosis, hypothermia, and stress.
Similarly, the microscopic findings in SARS-CoV-2 patients included diffuse alveolar damage with exudates. The inflammation was predominantly lymphocytic, and multinucleated giant cells were seen alongside large atypical pneumocytes, although no definitive viral inclusions were noted.
POSSIBLE INFERENCES:
ECMO IN CDH moribund Infants provides a means of maintaining oxygen delivery only temporarily, and its salvage rate depends on the reversibility of the pathologic factors that led to respiratory failure within the time frame that ECMO can be used. Although the pulmonary hypoplasia associated with CDH can be “outgrown”, the time required for this adaptive process often exceeds that provided by ECMO bypass. This accounts for the significant differences in survival observed between patients who have CDH and those who have more rapidly reversible causes of respiratory failure, including PPHN, meconium aspiration syndrome, and sepsis.
However, that may not be the case in critically ill SARS-CoV-2. Hopefully, the timely use of ECMO would lead to better clinical outcomes in critically ill SARS-CoV-2 patients as compared to CDH infants. More so considering that in the study of ECMO for ARDS in patients with Middle East Respiratory Syndrome Coronavirus (MERS-CoV), a similar coronavirus disease that emerged in 2012, a significant decrease of in-hospital mortality rate and length of intensive care unit (ICU) stay was found in patients treated with ECMO compared to those managed with conventional therapy.
References:
1. Brandon Michael Henry, Giuseppe Lippi. Poor survival with extracorporeal membrane oxygenation in acute respiratory distress syndrome (ARDS) due to coronavirus disease 2019 (COVID-19): Pooled analysis of early reports. J. Crit Care 2020 Apr 1 doi: 10.1016/j.jcrc.2020.03.011 [Epub ahead of print]
2. Nair J, Lakshminrusimha S. Update on PPHN: mechanisms and treatment. Semin Perinatol. 2014;38(2):78–91.
Competing interests: No competing interests