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Background: The declaration of the COVID-19 pandemic triggered a global inquiry into the transmission, mortality, risk factors, and management of the disease. Recently, however, attention has shifted toward its long-term consequences. There is a need for a better understanding of the predictors and symptoms of post-COVID syndrome, to ensure appropriate care for patients recovering from COVID-19 beyond the acute phase.
Methods: We searched PubMed, Google Scholar, Cochrane databases, and available data in the PROSPERO databases. We also explored the reference lists of included articles and any systematic reviews identified therein. We searched the keywords "Post Covid", "Post COVID syndrome", "Post- Covid" and "PostCOVID", until July 2021.
Results: Of 8167 articles, 13 were included. The syndrome affects several systems with variable prevalence. Fatigue and sleep disturbance is the most common symptom of acute post-COVID syndrome, observed in more than two-thirds of patients, while a reduction in quality of life and general health status was noted in up to 69%. Furthermore, a reduced aerobic and diffusion capacity was seen in 38% of patients up to one month after presumed recovery from infection. Radiologically, in up to 52% of patients, a ground-glass opacity (GGO) was noted beyond three months post-infection. The incidence of new psychiatric illness increased from as early as 14 days after infection and up to three or six months. Hearing impairment or loss, whether sensorineural or conductive, was noted in up to 8.3% of patients, and tinnitus was seen in up to 4.2% .
Conclusion: Overall, given the variability in the manifestation of post-COVID syndrome, a multidisciplinary team is required to better serve these patients. We therefore urge the establishment of such teams, encompassing internal medicine, pulmonology, cardiology, and neurocognitive services.
Keywords: Post COVID, Post COVID Complications, Post COVID Syndrome
The declaration of the COVID-19 pandemic triggered im- mediate inquiry into its transmission, mortality, risk factors, and management. Recently, however, attention has shifted toward its long-term consequences. Several reports highlight the issue of new or persistent symptoms several weeks after presumed recovery [1], the first report thereof probably being in May 2020 [2]. These reports describe an organised syn- drome that affects the multisystem in an unorganised fashion, termed "post-COVID-19 syndrome" [3]. The pathophysiology of post-COVID syndrome is believed to be multifactorial. It was proposed that the major contributors to the syndrome
Abdulmohsen Alhumayn, Ibrahim Alsaif, Sharafaldeen Bin Nafisah are with Emergency Department, King Fahd Medical City, e-mail: mohsen.alhumayn@gmail.com, e-mail: ebrahim771@hotmail.com, e-mail: dr.sharafaldeen@yahoo.com (Corresponding author: Abdulmohsen Alhu- mayn)
Joud Enabi is with Alfaisal University , e-mail: jenabi@alfaisal.edu
include, but are not limited to, microvascular ischaemia and injury, immobility, and metabolic alterations during the critical phase of infection [4]. It was also proposed that the syndrome be classified according to the timing of symptoms, degree of recovery, and complications [5]. The duration of symptoms prompted further classification, with symptoms of less than three months but more than five weeks referred to as acute post-COVID symptoms; more than three months but less than 24 weeks termed long post-COVID symptoms; and symptoms beyond 24 weeks referred to as persistent post-COVID symp- toms [6-8].
A proper understanding of this syndrome and its predictors is essential to develop an infrastructure capable of caring for those patients recovering from COVID-19 infection beyond the acute phase. It came to our attention that although the literature includes several systematic reviews concerning each system, the reporting of the symptoms of each system still lacks systematic inquiry. This systematic review therefore aims to explore the symptoms of post-COVID-19 and the predictors for its development.
Review question: What are the manifestations and the predictors of post-COVID syndrome?
Study Design: A systematic review of the systematic reviews of post-COVID syndrome.
Search Strategy: We searched PubMed, Google Scholar, Cochrane databases, and available data in the PROSPERO databases. We also explored the reference lists of included ar- ticles and any systematic reviews identified therein. Keywords searched were "Post Covid", "Post COVID syndrome", "Post- Covid", and "PostCOVID", from 1963 to July 2021.
Selection Criteria: Our inclusion criteria were all system- atic reviews of post-COVID syndrome articles that explored patients’ symptomatology, irrespective of the syndrome’s clas- sification. We excluded non-English articles that lacked trans- lation, and articles that were non-systematic reviews.
Data Extraction and Management: We screened titles and abstracts, extracted published articles, and retrieved data to analyse this systematic review. The studies’ eligibility for inclusion was examined by the authors separately; a meeting was then held in case of any disagreement regarding a study’s inclusion. The data was extracted on the basis of various factors, including the study’s time frame, patient population, investigations, interventions, and outcomes.
We used the Critical Appraisal Skills Programme (CASP) to assess the risk of bias for systematic review [9]. The analysis
was recorded following the Preferred Reporting Items for a Review and Meta-analysis of Individual Participant Data [10].
Data Synthesis and Summary Measures: We focused on including the descriptive measures of the various signs and symptoms among Post-COVID syndrome patients in each study, using the upper confidence interval limit. We also explored the predictors for the syndrome’s development.
RESOURCE : No funds, grants, or support were received.
IV. APPROVAL : This study was approved by the research committee, with IRB log number IRB00010471.
Of 8167 articles, 13 were included, as illustrated in the Prisma chart, Figure 1. The number of participants within each review and the number of articles is illustrated in Table 1, while Table 2 illustrates the risk of bias in those articles.
General health: Fatigue is the second-most common symptom of acute post- COVID syndrome, occurring in up to 73% of patients [11-13], secondary to sleep disturbance in 85% [11]. While fatigue is still prevalent in chronic post-COVID syndrome, dyspnoea is also prevalent in up to 64% of patients [11-13]. Nonetheless, fatigue was attributed to many factors, including respiratory muscle weakness, post-viral fatigue syndromes, and possi- ble general deconditioning [12]. Thus, the symptomatology may suggest overlaps with clinical presentation of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) [14]. However, any association or causation between post-COVID and those syndromes is yet to be determined, and thus far the similarity has only been suggested [14].
On the other hand, a reduction in quality of life and general health status was noted in up to 69% of patients from 14 days to three months post-infection [15]. In addition, there was a decline in the performance of activities of daily living (ADL) after COVID-19 infection, regardless of the scale applied [16]. Other non-specific symptoms that affect general health included arthralgia in up to 24% of patients, neuralgia in 38%, alopecia in 34%, and some had hyperhidrosis [13,17,18].
Respiratory system: A reduction in aerobic and diffusion capacity was observed in 38% of patients within one month after infection. Patients have persistent dyspnoea, cough and chest pain [19]. However, other explanations for the dyspnoea include the development of pulmonary fibrosis, dysfunctional breathing and respiratory muscle weakness that may persist up to eight weeks from recovery [11,12]. Residual signs of fibrosis, in particular, were responsible for exercise-induced desaturation [12].
Nevertheless, altered diffusion capacity is the most common pathology, seen in up to 55% of patients, followed by a restrictive pattern in 17% and an obstructive pattern in 9% [12,19]. It should be noted that 55% of patients will have an abnormal pulmonary function tests (PFT) [12]. However, there is an improvement in lung mechanics over time [19].
It should also be asserted that abnormal lung function and structural changes were seen up to six months post-infection [20].
Radiologically, in up to 52% of patients there is a ground- glass opacity (GGO) beyond three months post-infection [12]. During this period, up to 52% of patients’ CTs will reveal interstitial thickening or interlobular septal thickening [12]. In the same period, fibrous stripes were also common and seen in up to 44% of patients, with a similar percentage for bronchiec- tasis, in 43% [12]. Fibrotic-like changes, in particular, were seen up to 6 months post-infection, in up to 35% of patients [20]. Consolidation was less common, seen in only 11% [12]. Pleural thickening and bronchovascular bundle distortion were also seen, more commonly than consolation [12]. Autopsies of COVID-19 patients revealed varying degrees of destruction of alveolar structure, as well as pulmonary interstitial fibrosis [19].
Cardiovascular and haematological system: Myocardial inflammation was common, as noted in 78% [11]. This figure varies, however; some studies revealed a lower percentage of 26% [15]. Acute findings included non- specific interstitial oedema, with or without myocarditis [21]. However, such findings were not the cause of death in most patients, while hypertrophy or cardiac dilation was noted in the autopsies of those who did not survive [12]. Myocardial fibrosis was more common than myocardial infarction, venous or intracardiac thrombosis, amyloidosis, and inflammatory infiltrate not meeting the diagnosis of myocarditis. However, it was difficult to determine whether these symptoms were acute or overlapping with chronic pathology [12]. Hence, myocardial fibrosis might be the end result of any of the aforementioned cardiac injuries [12].
Symptomatically, chest pain occurred in up to 35% of patients. This may be a result of the abovementioned causes, or may be related to myocardial ischaemia, thrombosis, my- ocarditis, perimyocarditis or pericarditis [11,13]. The latter three pathologies appeared as late as three months after onset of symptoms of infection [15]. Even with apparently recovered cardiac function, there might still be a risk of coronary artery disease, atrial fibrillation or ventricular arrhythmias due to myocardial injury [15].
Neurological system and mental health: Headache beyond the infection period occurred in up to 78% of patients [11,13,17]. Other symptoms included sensorimotor disturbances, dizziness and vertigo [13,22].
The incidence of new psychiatric illness increased from as early as 14 days and up to three or six months post-infection [15,22]. Psychiatric conditions entailed anxiety in 26.8%, depression in 33%, post-traumatic stress disorder in 24.1%, insomnia and dementia, compared with an unaffected control group [11,15,22]. Cognitive impairment was observed in up to 35.7%, manifesting as inattention and impaired short-term memory, and was observed up to six months post infection [20]. Moreover, persistent neurological symptoms were noted in up to 55% of patients after three months [15]. On the other hand, the infection itself might trigger neurodegenerative diseases such as multiple sclerosis, Parkinson’s disease, and narcolepsy in the long term [15].
need for mechanical ventilation and ICU care [16].
At the time of this writing, this is the first comprehensive review of post-COVID syndrome. This review uncovered a broad range of symptoms that persist beyond assumed recov- ery from COVID infection. It is therefore prudent to explore the prevalence of such symptoms and their onset, in order to reduce the frequency of patient visits to the ED and to plan for subsequent care after discharge. Due to the variation in symptoms and the multiple systems affected post-COVID, it is also prudent to establish an interdisciplinary team to follows every patient with this syndrome.
The symptomatology of post-COVID syndrome varies in the literature; however, fatigue, dyspnoea and sleep disturbance are common in the early phase. Fatigue was indeed noted after several infections, including influenza A (H1N1) virus, SARS-CoV, Ebolavirus and West Nile virus [15]. Although fatigability might be multifactorial here, some advocate the implication of muscular atrophy and the use of steroids [24]. Dyspnoea was related to altered diffusion capacity, acutely, or the development of pulmonary fibrosis or respiratory muscle weakness. The chronic lung changes that occurred during the infection were responsible for the dyspnoea that occurred after resolution of the infection. Lung damage from other Coronavirus strains also manifested with dyspnoea [25]. It is assuring to note that the lung mechanics improve with time; however, it may require six months for complete improvement [20]. In this review, we noted that up to one-third of patients developed pulmonary fibrosis. Therefore, a follow up with advanced imaging is required in those presenting with the respiratory symptoms.
Several myocardial changes were also noted in relation to post-COVID syndrome. Myocarditis was also seen, but was not severe enough to be a cause of death [12]. Chest pain should be worked up for myocardial ischaemia, thrombosis, myocarditis, perimyocarditis and pericarditis [11,13]. Those with chest tightness will also require investigation for a secondary chest infection or stress-induced cardiomyopathy [26]. Because myocarditis was not common, it should not be among the top differential diagnoses as a cause of cardio- vascular deterioration [21]. Arrhythmias should also not be overlooked [15]. Moreover, due to the variation in post-Covid cardiovascular findings, MRI is warranted, whether on an acute emergency visit or as an inpatient.
Probably the least common manifestation of this syndrome is the otorhinolaryngological symptoms and the endocrinolog- ical and reproductive symptoms and, given the inconsistent findings, a follow-up should not be standardised.
Overall deconditioning should be expected, mandating fre- quent outpatient visits, and more involvement could be needed from the patient’s family or from social services. Furthermore, decreased functional status and dependency should be assessed regularly, as these were associated with short-term mortality [16].
The association of the initial presentation and higher symp- tom load with the development of this syndrome is a non- modifiable factor. With widespread vaccination, however, this may change. Nevertheless, patients with a severe presentation, especially with high inflammatory markers, should have reg- ular and more frequent follow-ups given their propensity for persistent lung abnormalities, neurocognitive impairment and fatigue, all of which lead to a decline in general health status. Whether the reduction in quality of life and general health status is related to dyspnoea or to fatigue and joint pain is yet to be determined. However, we believe it stems from multifactorial causes, including organic and psychological factors.
Overall, given the variability in the manifestation of post- COVID syndrome, a multidisciplinary team is needed to better serve these patients. We therefore urge the establishment of such teams, encompassing internal medicine, pulmonology, cardiology, and neurocognitive services.
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| Review | No. of participants | No. of studies referenced | Studies |
|---|---|---|---|
| within review | within review | ||
| Activities of daily living | 1465 | 9 | Pizarro-Pennarolli et |
| al. (2021) | |||
| Cardiovascular, respiratory, neurological and mental health | 12974 | 43 | Iqbal et al. (2021) |
| Cardiovascular | 322 | 41 | Roshdy et al. (2021) |
| Cardiovascular, respiratory, neurological, mental health, endocrine, | 3520 | 31 | Willi et al. (2021) |
| haematological and ENT | |||
| Cardiovascular, respiratory, neurological, mental health, endocrine, | 364 | 35 | Hoshijima et al. |
| haematological and ENT | (2021) | ||
| Neurological and mental health | 5795 | 21 | Wong and Weitzer |
| (2021) | |||
| Cardiovascular, respiratory, neurological, mental health, endocrine, | 47910 | 15 | Lopez-Leon et al. |
| haematological and ENT | (2021) | ||
| ENT | 1874 | 56 | Almufarrij and |
| Munro (2021) | |||
| Neurological and mental health | 18917 | 51 | Badenoch et al. |
| (2021) | |||
| Cardiovascular, respiratory, neurological, mental health, endocrine, | 54910 | 21 | Malik et al. (2021) |
| haematological and ENT | |||
| Respiratory | 5323 | 24 | Sanchez-Ramirez et |
| al. (2021) | |||
| Respiratory, neurological, mental health, endocrine, haematological, | 22289 | 145 | Salamanna et al. |
| ENT and activities of daily living | (2021) | ||
| Respiratory | 380 | 6 | Torres-Castro et al. |
| (2020) |
| Lead author Q1 Q2 Q3 Q4 | Q5 Q6 Q7 Q8 Q9 Q10 Fully achieved |
|---|---|
| Pizarro-Pennarolli et al. (2021) Y Y Y Y | Y P N Y Y Y 8 |
| Iqbal et al. (2021) Y Y P Y | Y Y Y Y Y Y 9 |
| Roshdy et al. (2021) Y Y Y P | Y Y N Y Y Y 8 |
| Willi et al. (2021) Y Y Y Y | Y Y N Y Y Y 9 |
| Hoshijima et al. (2021) Y Y P Y | Y Y Y Y Y Y 9 |
| Wong and Weitzer (2021) Y Y P Y | Y Y N Y Y Y 8 |
| Lopez-Leon et al. (2021) Y Y P Y | P Y P Y Y Y 7 |
| Almufarrij and Munro (2021) Y Y Y Y | Y P P Y Y Y 8 |
| Badenoch et al. (2021) Y Y Y Y | Y N N Y Y Y 8 |
| Malik et al. (2021) Y Y N Y | Y P N Y Y Y 7 |
| Sanchez-Ramirez et al. (2021) Y Y Y Y | Y P Y Y Y Y 9 |
| Salamanna et al. (2021) Y Y Y Y | Y N N Y N Y 7 |
| Torres-Castro et al. (2020) Y Y Y Y | Y Y P Y N Y 8 |
| Y: Yes; N: No; P: Partially | |
| Otorhinolaryngological system: | Endocrine manifestations included subacute thyroiditis, |
| Hearing impairment/loss, whether sensorineural or con- | hypothalamic-pituitary-thyroid axis dysfunction, diabetes sec- |
| ductive, was noted in up to 8.3% of patients [20,23]. The | ondary to pancreatic damage, and testicular dysfunction with |
| extent of impartment varies, but it appears to occur at high | associated infertility [15]. |
| frequencies [23]. Tinnitus was also noted in up to 4.2%, | |
| occurring intermittently or continuously [20]. Such symptoms | Predictors for the development of post-COVID syndrome: |
| may have been present before the infection, however, and | The worse the initial presentation, the more likely it is that |
| only exacerbated later on [23]. Non-specific vertigo, otalgia, | the patient will report functional impairment later on [11]. |
| otitis media, and other symptoms related to hypersensitivity | Moreover, the higher the symptom load, the more likely it will |
| and phonophobia were also noted [20,23]. Anosmia also | persist, and the more likely it will subsequently develop |
| occurred in post-COVID syndrome in up to 27% of patients | persistent fatigue associated with long term impairment [11]. |
| [11,13]. The olfactory dysfunction observed in these patients | However, some argued against the association of disease |
| follows a similar mechanism to that of the post-viral olfactory | severity with a higher prevalence of fatigue [12]. The need for |
| dysfunction seen in other common viral infections, such as | hospitalisation and the 40-49-year age segment were also |
| rhinovirus [15]. The olfactory and gustatory dysfunctions did | predictors for the development of post-COVID syndrome [11]. |
| not improve after one month, in 28% and 20% of patients | Higher mortality was observed in the short term among |
| retrospectively. The former persisted in up to 14.3% after the | patients with a low baseline score on the Barthel Index for |
| second month, and some cases remained up to six months | Activities of Daily Living (ADL), i.e., decreased functional |
| [20]. Ageusia was also reported in up to 28% of patients [11]. | status and dependency. This was seen among older age groups |
| and patients with a complicated hospital stay, including the | |
| The severity of the altered diffusion capacity is associated | Headache is known to be a common presentation of Covid- |
| with the development of pulmonary fibrosis. Moreover, high | 19 infection, and also in the post-infection period. Although |
| inflammatory markers signify severe disease [19]. Those with | 78% of patients developed a headache as part of their syn- |
| severe disease had persistent lung abnormalities on advanced | drome, it should trigger investigating for cerebral venous |
| imaging [12]. Increased oxygen requirement is associated with | thrombosis as well, given the thrombogenicity of the virus |
| ground-glass opacification/opacity and the diffusing capacity | [27]. |
| of the lungs for carbon monoxide (DLCO) [12]. Symptomati- | New-onset psychiatric illness was not uncommon, and |
| cally, residual abnormalities in CXR correlated with persisting | mental health assessment should be included in the patient’s |
| respiratory symptoms up to six months post-infection [20]. | follow-up. While more than half the patients had a persistent |
| In addition, moderate to severe COVID is associated with | neurological deficit after three months, we noted that cognitive |
| neurocognitive impairment in up to 37% of patients for a | impairment was seen up to six months [15,20]; this mandates |
| period of up to six months [20]. The prevalence of neuralgia | the integration of a neurocognitive service in the follow-up |
| appears to increase with time [13]. Moreover, non-hospitalised | period. |
| patients were more likely to develop anxiety [22]. | Probably the least common manifestation of this syndrome |
| is the otorhinolaryngological symptoms and the endocrinolog- |