Next Article in Journal
Can Intergroup Contact in Virtual Reality (VR) Reduce Stigmatization Against People with Schizophrenia?
Next Article in Special Issue
Risk Factors Associated with 30-Day Mortality in Older Patients with Influenza
Previous Article in Journal
Comparison of Holmium:YAG and Thulium Fiber Lasers on the Risk of Laser Fiber Fracture
Previous Article in Special Issue
Flexible Modeling of Net Survival and Cure by AML Subtype and Age: A French Population-Based Study from FRANCIM
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Chronology of COVID-19 Symptoms in Very Old Patients: Study of a Hospital Outbreak

1
Service de Gériatrie à Orientation Cardiologique et Neurologique, AP-HP, Sorbonne Université, Hôpitaux Universitaires Pitie-Salpêtrière-Charles Foix, F-94200 Ivry-sur-Seine, France
2
Clinical Epidemiology and Ageing (CEpiA) Unit, INSERM U955, Institut Mondor de Recherche Biomédicale, F-9410 Créteil, France
3
Unité de Gériatrie Aigue, AP-HP, Sorbonne Université, Hôpital Rothschild, F-75012 Paris, France
4
Service de Soins de Suite et de Réadaptation Gériatrique, AP-HP, Sorbonne Université, Hôpitaux Universitaires Pitie-Salpêtrière-Charles Foix, F-94200 Ivry-sur-Seine, France
*
Author to whom correspondence should be addressed.
J. Clin. Med. 2021, 10(13), 2962; https://doi.org/10.3390/jcm10132962
Submission received: 18 June 2021 / Revised: 26 June 2021 / Accepted: 29 June 2021 / Published: 30 June 2021
(This article belongs to the Special Issue Acute Care and Medication Management in Older Adults)

Abstract

:
Background: We wanted to better understand the frequency and temporal distribution of symptoms of COVID-19 in very old patients, which are currently not well defined. Methods: In an observational, descriptive study, we followed all patients being at three geriatric convalescence and rehabilitation units when a COVID-19 outbreak emerged in those units in March 2020. For those who developed the disease, we recorded any new symptom occurring at diagnosis, in the previous 14 and the following 21 days. A group of SARS-Cov-2-negative patients served as controls. Results: Sixty-nine of the 176 inpatients (mean age: 86 years) were infected by SARS-Cov-2 during the outbreak. At the moment of diagnosis, a majority of patients had fever (71.0%), malaise-asthenia (24.6%), or respiratory symptoms (66.7%). However, 48 patients (69.6% of all SARS-Cov-2 positive patients) also presented, usually several days before, other symptoms: (a) gastrointestinal symptoms (39.1% of all patients, median onset eight days before diagnosis, IQR −9 to +3 days); (b) neurological symptoms (30.4% of all patients, median onset five days before diagnosis, IQR −11 to −3 days), notably delirium (24.6%); and (c) other symptoms, like falls and unexplained decompensation of chronic conditions (29.0% of all patients, median onset four days before diagnosis, IQR −10 to 0). None of those symptoms were observed in similar proportion in 25 control SARS-CoV-2-negative patients, hospitalized during the same period. Conclusions: Diarrhea, nausea-vomiting, delirium, falls, and unexplained decompensation of chronic conditions were the first symptoms of COVID-19 in a majority of older patients in this cohort, preceding typical symptoms by several days. Recognizing those early symptoms could hasten the diagnosis of COVID-19 in this population.

1. Introduction

Older patients constitute a substantial proportion of all COVID-19 patients, develop severe disease more frequently, and cumulate a majority of the deaths caused by COVID-19, especially if very old or frail [1,2,3,4,5]. The extent to which the clinical presentation of COVID-19 may be different in older patients is not well known. Published studies to date have reached inconsistent results. Some studies, including a small series, a retrospective cohort, and a national cross-sectional study, have found that atypical symptoms, like diarrhea, falls, and delirium, were more frequent in older patients [6,7], especially in frail ones [8]. This was also the impression of some clinicians who had treated older COVID-19 patients [9]. However, other series and large studies found either no difference compared with younger patients [10,11], or found, as the only difference, that typical symptoms (fever, malaise, respiratory) were less frequent in older patients [12,13,14]. Solving those discordances is important, as not recognizing early symptoms of COVID-19 might lead to delayed diagnosis and treatment, as well as allowing more time to further spread the infection between contacts.
In mid-March 2020, as the COVID-19 pandemic wave reached the Paris area, France, outbreaks of COVID-19 developed in several geriatric rehabilitation units, affecting patients who had been initially hospitalized for other causes. That provided us a unique opportunity to observe and follow the clinical characteristics of COVID-19 as they developed in those patients. Therefore, we decided to systematically record any symptom that appeared, and its time of onset, in all patients who acquired COVID-19, as well as in a control group of patients who tested negative for SARS-CoV-2, to better define which were the most frequent symptoms of COVID-19 in older people, and to determine if those symptoms followed any temporal pattern.

2. Methods

This was an observational study, with a retrospective cohort, conducted in three geriatric rehabilitation and convalescence units, totaling 176 beds, located at two hospitals, in the Paris area, France.
Patients included were older adults (>75 years old) who were hospitalized at the participating units and developed SARS-CoV-2 infection during their stay. Patients had been initially hospitalized for a variety of medical conditions and had been transferred from acute care because they needed rehabilitation or more time to recover. After the first Covid-19 cases appeared, all patients who had been in contact with them were systematically tested, whether symptomatic or not, as well as any patient subsequently presenting any new or unusual symptom, of any severity, even very mild. All diagnostic were made by detecting SARS-CoV-2 specific ARN (E gen and/or Orf region) in nasopharyngeal swab samples, using an automated PCR Cobas® 6800 System assay (Roche Ltd., Basel, Switzerland).
For each COVID-19 patient, we retrieved and recorded, using a predefined form, any new clinical sign or symptom that was present at the time of diagnosis, have been noticed in the previous 14 days or appeared in the following 21 days, as well as the moment it appeared. Data were retrieved prospectively from the moment of diagnostic for some patients, but retrospectively from their medical records for others. In addition, in order to differentiate those signs and symptoms from other acute complications frequent in geriatric patients (e.g., other infections), we also retrieved symptoms, in the same way, in all patients who were in one of the participating units at the beginning of the outbreak but who tested negative for SARS-CoV-2. Variables in both groups (COVID-19 and controls) were compared using Fisher exact test (for frequencies) or a Wilcoxon rank sum test (when numerical), employing STATA (v13, StataCorp LP, Texas, TX, USA). All tests were two-tailed and a p < 0.05 was considered significant.
All patients received written information about the use of their personal medical data for research purposes and could refuse at any moment to participate in the study. All data was anonymized. The French Commission Nationale Informatique et Libertés (CNIL) authorized the use of medical data for this study (Declaration number: 2218210v0). The study was conducted in full accordance with the Declaration of Helsinki. We followed the STROBE statement for improving the reporting of observational studies while writing this manuscript [15]. A completed STROBE checklist is available from the authors upon request.

3. Results

After the first PCR-confirmed COVID-19 case, on March 19, 2020, the number of cases quickly increased and reached a peak eight days later. An enquiry found no preceding suspected cases in patients or in hospital staff, but at least two confirmed Covid-19 cases in relatives who had recently visited their loved ones (visits were later forbidden, in 12 March). We concluded that the disease had probably been introduced by visiting relatives, then involuntarily disseminated among in-patients by caregivers and patient-to-patient contact. A separate division was created to host and isolate all COVID-19 patients and after 20 April no new case appeared for the following four weeks, when this study was closed.
In the end, 69 of the 176 inpatients (39.2%) acquired a confirmed SARS-CoV-2 infection during the study period (Figure 1). Mean age was 86 (SD ±6.4) years. Six patients (8.7%) were asymptomatic at all times. They were tested, and thus diagnosed, because have been in contact with known cases. The characteristics of patients and the distribution of symptoms are shown in Table 1.
The most frequent symptoms were fever, associated or not with general symptoms (71.0% of patients), and respiratory symptoms (66.7% of patients). Eighteen patients (26.1%) had oxygen desaturation at least at one moment, but only four patients (5.8%) developed overt respiratory failure. Fever, general and respiratory symptoms usually appeared at the same time, as shown in Figure 2, and prompted the diagnosis of COVID-19 in most patients. Overall, 57 patients (82.6%) had one (or several) of those symptoms.
In the horizontal axis, the 0 point corresponds to the moment COVID-19 was diagnosed. Negative numbers denote an onset of symptoms prior to COVID-19 diagnosis, positive numbers an onset of symptom afterwards.
In addition, 48 patients (69.6%) presented symptoms other than fever, general or respiratory. Twenty seven patients (39.1%) had gastrointestinal symptoms, diarrhea being by large the most frequent (34.8% of all patients). Twenty one (30.4%) presented neurological symptoms, particularly the appearance of unexplained delirium (24.6% of all patients) and less frequently behavioural disturbances (7.2%). Finally, some patients had other, diverse symptoms, such as falls (15.6% of patients) and sudden decompensation of previously stable chronic diseases, predominantly of heart failure (13.0%). None of those symptoms happened with similar frequency in control, COVID-19-negative patients, during the study period.
A distinctive temporal pattern appeared when analyzing the time of onset of each symptom, as shown in Table 1 and Figure 2. Gastrointestinal, neurological, and other symptoms tended to appear early in the course of disease, preceding fever and respiratory symptoms by several days: neurological symptoms appeared a median of eight days before (interquartile range (IQR) −11 to −3); gastrointestinal symptoms a median of five days before (IQR −9 days before to +3 days after); and other symptoms (falls, heart failure) a median of four days before (IQR −10 to 0).

4. Discussion

In this study, we found that a great proportion of older patients had other symptoms than fever and respiratory. Almost 40% also had gastrointestinal symptoms and about 30% presented neurological or other symptoms. Diarrhea, occurrence of unexplained delirium and falls were respectively the leading symptom in each group. These symptoms are relatively frequent in older patients, as they can be caused by a variety of conditions, but none of them happened with similar frequency in the control group during the same period.
The main finding of our study, however, is a definite temporal pattern: gastrointestinal, neurological, and other atypical symptoms had a clear tendency to appear early in the course of the infection. They preceded by several days the appearance of fever and respiratory symptoms, which, in most cases, were the symptoms that finally led us to diagnosing COVID-19. Luo et al. also found that gastrointestinal symptoms were often the first symptoms appearing [16]. No other study, however, has reported a similar temporal distribution of symptoms, to the best of our knowledge. Fever, respiratory symptoms, general symptoms (fatigue, myalgia, asthenia …), and anosmia are reported in virtually all studies as the first symptoms appearing in COVID-19 [1,2,3,4,5,6,7,8,9,10,11,12,13,17]. Larsen et al. specifically studied the order of symptoms onset in a dataset of more than 55,000 COVID-19 patients from China and found that the most likely order of occurrence of symptoms was fever, cough, nausea/vomiting, and diarrhea [18]. Most patients in the dataset they employed were young adults, however, and a separate analysis of older adults was not conducted.
Additionally, our findings confirm those from other studies indicating that atypical symptoms of COVID-19 are more frequent in older patients [6,7]. Gastrointestinal and neurologic syndromes have been well described in COVID-19 patients but less frequently. Gastrointestinal symptoms have been found in 11–19% of all patients [2,16,19,20]. Neurological symptoms have been reported less consistently and in just between 3% and 9% of patients, if we exclude unspecific symptoms like headache and dizziness [1,2,21,22,23]. Published studies in older patients have found inconsistent results regarding the type and frequency of COVID-19 symptoms [5,6,7,8,9,10,11,12,13]. These discrepancies are probably due to variations in the characteristics of included patients, setting of the study and methods employed. The mean age of included patients, for instance, varied largely, ranging from 67 to 86.5 years. Another important factor is frailty, which has been associated COVID-19 severity and variations in clinical features [3,4,7]. Patients in our study were very old (mean 86 years) and, although we did not formally assess frailty, most of them had chronic conditions and limitations in their autonomy that would qualify them as frail. In any case, several published studies have also found that atypical presentations were more frequent in older persons [5,6,11,12,13]. None of those studies, however, analyzed the order of symptoms onset. In most of them symptoms were only assessed at inclusion.
The fact that the chronology of symptoms may be very different in very old persons has important clinical implications, as recognizing those first, less typical symptoms might allow to diagnose COVID-19 several days earlier in many of those patients. An early diagnosis is important, not only for starting proper treatment of affected patients, but also in order to rapidly implement control measures to limit the virus spreading. The latter is essential in these settings, at hospitals and nursing homes, where many older persons stay together, to limit the number of persons contaminated. In this regard, it must be noted that, as in other studies in older patients [24,25], some of our patients showed active nasopharyngeal excretion of SARS-CoV-2, as confirmed by PCR, but were completely asymptomatic, even though they were very old and fragile.
Our work has clear limitations: the number of patients included is limited, they were very old and most of them had diverse chronic conditions, part of the data was retrieved retrospectively, and older patients were not directly compared with younger ones. Consequently, it remains uncertain whether our findings could be applied to the general population of frail or very old patients. Further studies would be needed to confirm its generalizability. Assessing frailty status in those studies would be important. As strengths, including all patients involved in an outbreak allowed us to study patients from the whole spectrum of severity of the disease, as well as methodically retrieve any symptom appearing during the entire clinical course of the disease.
In conclusion, in this cohort of very old patients with COVID-19, the first symptoms of COVID-19 in a majority of patients (more than two thirds) were gastrointestinal, neurological, and other atypical symptoms, particularly delirium, falls, and sudden decompensation of chronic conditions. Those symptoms showed a definite temporal pattern, usually appearing several days before fever and respiratory symptoms. Recognizing this temporal pattern could hasten the diagnosis of COVID-19 in older patients by several days.
More research remains necessary to know if COVID-19 symptoms follow a similar pattern in other groups of older patients.

Author Contributions

C.L.-L.: conception and design, analysis and interpretation of data, statistical analysis, critical revision of the manuscript, supervision. Q.D.N.: acquisition of data, analysis and interpretation of data, drafting of the manuscript. H.K.: acquisition of data, statistical analysis, technical support. S.O.-F.: acquisition of data, analysis and interpretation of data, technical support. M.M.: acquisition of data, statistical analysis, administrative support. B.O.: acquisition of data, technical support, critical revision of the manuscript. C.D.: acquisition of data, critical revision of the manuscript. A.R.: acquisition of data, analysis and interpretation of data, drafting of the manuscript. J.B.: conception and design, analysis and interpretation of data, critical revision of the manuscript, obtaining funding, supervision. All authors have read and agreed to the published version of the manuscript.

Funding

Assistance Publique—Hôpitaux de Paris, Paris, France. Sorbonne Université, Paris, France.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki, and approved by the Institutional Review Board (“Comité de Protection des Personnes”) of Ile-de-France XI (protocole 2020-A00754-35, 30 March 2020).

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

The data presented in this study are openly available in the Open Science Framework at DOI:10.17605/OSF.IO/WQC79, reference number WQC79.

Conflicts of Interest

None of the authors have any conflict of interest to declare regarding this work.

References

  1. Cummings, M.J.; Baldwin, M.R.; Abrams, D.; Jacobson, S.D.; Meyer, B.J.; Balough, E.M.; Aaron, J.G.; Claassen, J.; Rabbani, L.E.; Hastie, J.; et al. Epidemiology, clinical course, and outcomes of critically ill adults with COVID-19 in New York City: A prospective cohort study. Lancet 2020, 395, 1763–1770. [Google Scholar] [CrossRef]
  2. Zhou, F.; Yu, T.; Du, R.; Fan, G.; Liu, Y.; Liu, Z.; Xiang, J.; Wang, Y.; Song, B.; Gu, X.; et al. Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: A retrospective cohort study. Lancet 2020, 395, 1054–1062. [Google Scholar] [CrossRef]
  3. Hewitt, J.; Carter, B.; Vilches-Moraga, A.; Quinn, T.J.; Braude, P.; Verduri, A.; Pearce, L.; Stechman, M.; Short, R.; Price, A.; et al. The effect of frailty on survival in patients with COVID-19 (COPE): A multicentre, European, observational cohort study. Lancet Public Health 2020, 5, e444–e451. [Google Scholar] [CrossRef]
  4. Blomaard, L.C.; van der Linden, C.M.J.; van der Bol, J.M.; Jansen, S.W.M.; Polinder-Bos, H.A.; Willems, H.C.; Festen, J.; Barten, D.G.; Borgers, A.J.; Bos, J.C.; et al. Frailty is associated with in-hospital mortality in older hospitalised COVID-19 patients in the Netherlands: The COVID-OLD study. Age Ageing 2021, 50, 631–640. [Google Scholar] [CrossRef] [PubMed]
  5. COVIDSurg Collaborative. Mortality and pulmonary complications in patients undergoing surgery with perioperative SARS-CoV-2 infection: An international cohort study. Lancet 2020, 396, 27–38. [Google Scholar] [CrossRef]
  6. Godaert, L.; Proye, E.; Demoustier-Tampere, D.; Coulibaly, P.S.; Hequet, F.; Dramé, M. Clinical characteristics of older patients: The experience of a geriatric short-stay unit dedicated to patients with COVID-19 in France. J. Infect. 2020, 81, e93–e94. [Google Scholar] [CrossRef] [PubMed]
  7. Annweiler, C.; Sacco, G.; Salles, N.; Aquino, J.-P.; Gautier, J.; Berrut, G.; Guérin, O.; Gavazzi, G. National French Survey of Coronavirus Disease (COVID-19) Symptoms in People Aged 70 and Over. Clin. Infect. Dis. 2021, 72, 490–494. [Google Scholar] [CrossRef]
  8. Osuafor, C.N.; Davidson, C.; Mackett, A.J.; Goujon, M.; Van Der Poel, L.; Taylor, V.; Preller, J.; Goudie, R.J.B.; Keevil, V.L. Clinical Features, Inpatient Trajectories and Frailty in Older Inpatients with COVID-19: A Retrospective Observational Study. Geriatrics 2021, 6, 11. [Google Scholar] [CrossRef] [PubMed]
  9. Graham, J. Seniors with COVID-19 Show Unusual Symptoms. Available online: https://www.medscape.com/viewarticle/929407#vp_1 (accessed on 2 June 2020).
  10. Liu, K.; Chen, Y.; Lin, R.; Han, K. Clinical features of COVID-19 in elderly patients: A comparison with young and middle-aged patients. J. Infect. 2020, 80, e14–e18. [Google Scholar] [CrossRef] [Green Version]
  11. Covino, M.; De Matteis, G.; Santoro, M.; Sabia, L.; Simeoni, B.; Candelli, M.; Ojetti, V.; Franceschi, F. Clinical characteristics and prognostic factors in COVID-19 patients aged ≥80 years. Geriatr. Gerontol. Int. 2020, 20, 704–708. [Google Scholar] [CrossRef]
  12. Zhao, M.; Wang, M.; Zhang, J.; Gu, J.; Zhang, P.; Xu, Y.; Ye, J.; Wang, Z.; Ye, D.; Pan, W.; et al. Comparison of clinical characteristics and outcomes of patients with coronavirus disease 2019 at different ages. Aging 2020, 12, 10070–10086. [Google Scholar] [CrossRef]
  13. Kimball, A.; Hatfield, K.M.; Arons, M.; James, A.; Taylor, J.; Spicer, K.; Bardossy, A.C.; Oakley, L.P.; Tanwar, S.; Chisty, Z.; et al. Asymptomatic and Presymptomatic SARS-CoV-2 Infections in Residents of a Long-Term Care Skilled Nursing Facility—King County, Washington, March 2020. MMWR. Morb. Mortal. Wkly. Rep. 2020, 69, 377–381. [Google Scholar] [CrossRef] [Green Version]
  14. Guo, T.; Shen, Q.; Guo, W.; He, W.; Li, J.; Zhang, Y.; Wang, Y.; Zhou, Z.; Deng, D.; Ouyang, X.; et al. Clinical Characteristics of Elderly Patients with COVID-19 in Hunan Province, China: A Multicenter, Retrospective Study. Gerontology 2020, 66, 467–475. [Google Scholar] [CrossRef]
  15. von Elm, E.; Altman, D.G.; Egger, M.; Pocock, S.J.; Gøtzsche, P.C.; Vandenbroucke, J.P. STROBE Initiative. The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: Guidelines for reporting observational studies. J. Clin. Epidemiol. 2008, 61, 344–349. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  16. Jin, X.; Lian, J.S.; Hu, J.H.; Gao, J.; Zheng, L.; Zhang, Y.M.; Hao, S.R.; Jia, H.Y.; Cai, H.; Zhang, X.L.; et al. Epidemiological, clinical and virological characteristics of 74 cases of coronavirus-infected disease 2019 (COVID-19) with gastrointestinal symptoms. Gut 2020, 69, 1002–1009. [Google Scholar] [CrossRef] [Green Version]
  17. Luo, S.; Zhang, X.; Xu, H. Don’t Overlook Digestive Symptoms in Patients With 2019 Novel Coronavirus Disease (COVID-19). Clin. Gastroenterol. Hepatol. 2020, 18, 1636–1637. [Google Scholar] [CrossRef]
  18. Pan, L.; Mu, M.; Yang, P.; Sun, Y.; Wang, R.; Yan, J.; Li, P.; Hu, B.; Wang, J.; Hu, C.; et al. Clinical Characteristics of COVID-19 Patients With Digestive Symptoms in Hubei, China: A Descriptive, Cross-Sectional, Multicenter Study. Am. J. Gastroenterol. 2020, 115, 766–773. [Google Scholar] [CrossRef]
  19. Mao, L.; Jin, H.; Wang, M.; Hu, Y.; Chen, S.; He, Q.; Chang, J.; Hong, C.; Zhou, Y.; Wang, D.; et al. Neurologic Manifestations of Hospitalized Patients With Coronavirus Disease 2019 in Wuhan, China. JAMA Neurol. 2020, e201127. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  20. Montalvan, V.; Lee, J.; Bueso, T.; De Toledo, J.; Rivas, K. Neurological manifestations of COVID-19 and other coronavirus infections: A systematic review. Clin. Neurol. Neurosurg. 2020, 194, 105921. [Google Scholar] [CrossRef]
  21. Wang, L.; Shen, Y.; Li, M.; Chuang, H.; Ye, Y.; Zhao, H.; Wang, H. Clinical manifestations and evidence of neurological involvement in 2019 novel coronavirus SARS-CoV-2: A systematic review and meta-analysis. J. Neurol. 2020, 267, 2777–2789. [Google Scholar] [CrossRef] [PubMed]
  22. Cohen, P.A.; Hall, L.E.; John, J.N.; Rapoport, A.B. The Early Natural History of SARS-CoV-2 Infection: Clinical Observations From an Urban, Ambulatory COVID-19 Clinic. Mayo Clin. Proc. 2020, 95, 1124–1126. [Google Scholar] [CrossRef]
  23. Larsen, J.R.; Martin, M.R.; Martin, J.D.; Kuhn, P.; Hicks, J.B. Modeling the Onset of Symptoms of COVID-19. Front. Public Health 2020, 8, 473. [Google Scholar] [CrossRef] [PubMed]
  24. Roxby, A.C.; Greninger, A.L.; Hatfield, K.M.; Lynch, J.B.; Dellit, T.H.; James, A.; Taylor, J.; Page, L.C.; Kimball, A.; Arons, M.; et al. Outbreak Investigation of COVID-19 Among Residents and Staff of an Independent and Assisted Living Community for Older Adults in Seattle, Washington. JAMA Intern. Med. 2020, 180, 1101–1105. [Google Scholar] [CrossRef] [PubMed]
  25. Arons, M.M.; Hatfield, K.M.; Reddy, S.C.; Kimball, A.; James, A.; Jacobs, J.R.; Taylor, J.; Spicer, K.; Bardossy, A.C.; Oakley, L.P.; et al. Presymptomatic SARS-CoV-2 Infections and Transmission in a Skilled Nursing Facility. N. Engl. J. Med. 2020, 382, 2081–2090. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Inclusion of patients.
Figure 1. Inclusion of patients.
Jcm 10 02962 g001
Figure 2. Temporal distribution of the onset of symptoms, by type.
Figure 2. Temporal distribution of the onset of symptoms, by type.
Jcm 10 02962 g002
Table 1. Signs and symptoms of COVID-19 in included patients.
Table 1. Signs and symptoms of COVID-19 in included patients.
Confirmed COVID-19 Patients
(n = 69)
PCR Negative Patients
(n = 25)
VariablePatients
N (%)
Onset of Symptom to COVID-19 Diagnostic (Days)
Median (IQR)
Patients
N (%)
Onset of Symptom to First PCR Test (Days)p
Patients characteristics
Age (mean, ±SD)86 ± 6.4-82 ± 4.8-ns
Women43 (75.4)-26 (70.3)-ns
ADL score (mean, ±SD)3.25 ± 2.1-Not available--
IADL score (mean, ±SD)2.6 ± 2.5-Not available--
Heart failure26 (37.7)-8 (32.0)-ns
Coronary disease16 (23.2)-0-0.008
Chronic lung disease13 (18.8)-0-0.02
Cerebrovascular disease19 (27.5)-7 (28.0)-ns
Dementia32 (46.4)-15 (31.9)-ns
Cancer6 (8.7)-6 (24.0)-0.049
Presenting symptoms
No symptom at all6 (8.7)-21 (84.0)--
Fever, general symptoms49 (71.0)0 (0 to 0)1 (4.0)0<0.001
Fever46 (66.7)0 (0 to 0)1 (4.0)0<0.001
Malaise, asthenia17 (24.6)0 (-2 to 1)0-0.048
Myalgia2 (2.9)−2.5 (−5 to 0)1 (4.0)0ns
Respiratory46 (66.7)0 (0 to 1)2 (8.0)0 (both)<0.001
Cough32 (46.4)0 (0 to 0)1 (4.0)0<0.001
Oxygen desaturation18 (26.1)1 (−4 to 2)0-0.002
Dyspnoea 14 (20.3)0 (0 to 2)0-<0.017
Abnormal lung sounds14 (20.3)1 (0 to 2)1 (4.0)0ns
Respiratory failure4 (5.8)2 (1 to 3)0-ns
Gastrointestinal27 (39.1)−5 (−9 to 3)0-<0.001
Diarrhea24 (34.8)−3 (−7 to 4)0-<0.001
Nausea, vomiting8 (11.6)−1 (−9 to 3)0-ns
Abdominal pain4 (5.8)−11 (−17 to 11)0-ns
Anorexia2 (2.9)−14 (both patients)0-ns
Neurological21 (30.4)−8 (−11 to −3)2 (8.0)-0.029
Delirium17 (24.6)−7 (−8 to −3)2 (8.0)−2 and 7ns
New behavioural disorder5 (7.2)−11 (−13 to −3)0-ns
Anosmia1 (1.4)00-ns
Other symptoms20 (29.0)−4 (−10 to 0)3 (12.0)-ns
Fall, syncope11 (15.9)−4 (−12 to 1)2 (8.0)−2 and 21ns
Heart failure decompensation9 (13.0)−3 (−8 to 0)1 (4.0)−6ns
Outcome (at 30 days after inclusion)
Dead10 (14.5)-1 (4.0)-ns
ADL = Activities of daily living, IADL = Instrumental activities of daily living, IQR = Interquartile range, ns = Not significant.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Lafuente-Lafuente, C.; Nghiem, Q.D.; Keravec, H.; Oukbir-Ferrag, S.; Magri, M.; Oquendo, B.; Donadio, C.; Rainone, A.; Belmin, J. Chronology of COVID-19 Symptoms in Very Old Patients: Study of a Hospital Outbreak. J. Clin. Med. 2021, 10, 2962. https://doi.org/10.3390/jcm10132962

AMA Style

Lafuente-Lafuente C, Nghiem QD, Keravec H, Oukbir-Ferrag S, Magri M, Oquendo B, Donadio C, Rainone A, Belmin J. Chronology of COVID-19 Symptoms in Very Old Patients: Study of a Hospital Outbreak. Journal of Clinical Medicine. 2021; 10(13):2962. https://doi.org/10.3390/jcm10132962

Chicago/Turabian Style

Lafuente-Lafuente, Carmelo, Quoc Duy Nghiem, Héloïse Keravec, Sihem Oukbir-Ferrag, Maurizio Magri, Bruno Oquendo, Cristiano Donadio, Antonio Rainone, and Joël Belmin. 2021. "Chronology of COVID-19 Symptoms in Very Old Patients: Study of a Hospital Outbreak" Journal of Clinical Medicine 10, no. 13: 2962. https://doi.org/10.3390/jcm10132962

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop