The 4th Udayana International Nursing Conference (4th INC)
Más datosIndonesia was one of the countries with the highest COVID-19 positive cases. Understanding the length of hospitalisation is critical for anticipating bed demand and resource allocation, such as oxygen. This study aims to examine the determinants of oxygen saturation and the length of hospitalisation in Hermina Mekarsari Hospital, West Java, Indonesia.
MethodsThis cross-sectional study uses medical records from June to August 2021. The inclusion criteria were: COVID-19 patients aged between18 and 65, fully conscious, and not using mechanical ventilation. Participants who passed away during hospital stay were excluded. We used demographic information, laboratory data, and the clinician's assessments of the patients admitted to the hospital. Linear regression was performed for oxygen saturation on day seven, while logistic regression analysis was conducted to predict the length of hospital stay.
ResultsIn total, 371 participants with an average age of 47.2 (standard deviation 15.8) years were included. Most participants were female (57.7%) and smoking (78.4%). The results indicated that decreasing oxygen saturation was reported in vomiting patients (β=1.63, p-value=.001), hypertensive patients (β 1.18 with, p-value=.034), and patients with the increased respiratory rate (β=0.28, p-value=.000). In the logistic regression, we found that respondents who experienced dyspnoea, headache, fever, an increasing number of D-Dimer and blood glucose, and those with diabetes mellitus were more likely to stay more than 14 days.
ConclusionsOxygen saturation was influenced by vomiting, hypertension, and increasing respiratory rate. Length of hospitalisation of more than 14 days was influenced by dyspnoea, headache, fever, increased number of D-Dimer, blood glucose, and diabetes mellitus. Identifying the determinants of oxygen saturation and length of stay can inform health professionals in designing a suitable intervention to reduce mortality and length of stay among COVID-19 patients in Indonesia.
The novel coronavirus disease 2019 (COVID-19) was first discovered in Wuhan in December 2019 before spreading worldwide. In Indonesia, the deaths related to COVID-19 reached 143,592 cases from a total of 4,249,323 positive cases.1 In mid-2020, World Health Organization (WHO) reported that the number of cases in Indonesia increased by 50% or more.1 From January to April 2022, the total number of cases was 6,015,748, with 155,164 deaths.1
A previous study pointed out that 57% of deaths due to COVID-19 occurred in men aged between 18 and 59, with a cumulative mortality rate of 13 deaths in every 100,000 people.2 WHO reported that Indonesia's health system was under tremendous strain due to the rising prevalence of COVID-19, including the supply of oxygen (WHO, 2021). Oxygen saturation≤90% predicts mortality among COVID-19 patients with respiratory distress after oxygenation.2 Therefore, it is crucial to determine the risk variables associated with oxygen saturation in the triage of patients.
Hospitalisation due to COVID-19 profoundly affected global health systems, i.e., overcrowding health facilities, demanding many health experts, causing burnout, and rising health finance and medical costs.3 A previous investigation has revealed that in Ghana, the presence of hypertension and diabetes mellitus influenced the length of stay among COVID-19 patients.4 However, their data is limited to only participants’ characteristics and comorbidities as the predictor. A more thorough understanding of the determinants of the length of hospitalisation is critical for anticipating bed demand and resource allocation, especially in resource-constrained settings. To fill the gaps and support the health care services, this study aims to identify the determinants of oxygen saturation and length of hospitalisation among COVID-19 patients in Indonesia.
MethodsThis cross-sectional study uses data from the medical record in Hermina Mekarsari Hospital, West Java, Indonesia. West Java was the province where the first COVID-19 cases were confirmed.5 The data were collected in the second wave of the epidemic, between May and August 2022, when the number of COVID-19 cases increased from an average of 1170 cases per week to 6949 cases per week in West Java. The inclusion criteria were: (a) COVID-19 positive, (b) aged between 19 and 64, (c) fully conscious, and (d) not using mechanical ventilation. We excluded participants who passed away during their treatment at the hospital.
The sample size was calculated based on the previous study, reporting an odds ratio (OR) of 0.2 between comorbidities on length of stay6 to achieve the power of 80% and a significance level of 0.05. We set the final sample size to at least 371 patients. We extracted demographic and health characteristic data, signs and symptoms, comorbidities, clinical assessment, and laboratory indices from medical records when patients were admitted to the hospital. The study protocol was approved by The Ethical Review Board of Saint Carolus Health Science, Indonesia (No. 005/KEPPKSTIKSC/I/2022).
We analysed the data using the Statistical Package for the Social Sciences for Windows (version 26.0; SPSS, Chicago, IL). The descriptive statistics were analysed using percentage, frequency, mean, and standard deviation to report the distribution of the variables. In bivariate analysis, we used a t-test to compare the mean between oxygen saturation and some potential factors, for instance, demographic and vital signs, signs and symptoms at admission, comorbid, and laboratory indices. We used linear regression to examine the factors of oxygen saturation among the COVID-19 patients, while binary logistics was used to analyse the clinical determinants of length of stay.
ResultsCharacteristics of participantsOf the 371 participants recruited, all completed the survey. The characteristics of the participants are described in Table 1. The results indicated that most participants were female, smoking, had several symptoms for instance dry cough, fever, tachipnoea. Additionally, most of the participant also had comorbidity.
Participants’ characteristics.
Variables | Frequency (n=371) | Percentage (%) (n=371) |
---|---|---|
Age, Mean (SD) | 47.2 | 15.8 |
Gender | ||
Female | 214 | 57.7 |
Male | 157 | 42.3 |
Smoking | ||
Yes | 291 | 78.4 |
No | 80 | 21.6 |
Haemoglobin, Mean (SD) | 13.1 | 7.5 |
Thrombocyte, Mean (SD) | 276,044.4 | 116,244.4 |
D-dimer, Mean (SD) | 481.1 | 557.1 |
Blood glucose, Mean (SD) | 152.5 | 116 |
Temperature, Mean (SD) | 37.5 | 1.0 |
Heart rate, Mean (SD) | 94.3 | 10.7 |
RR, Mean (SD) | 27.2 | 3.7 |
Systole, Mean (SD) | 124.8 | 15.9 |
Dry cough | ||
Yes | 328 | 88.4 |
No | 43 | 11.6 |
Fever | ||
Yes | 328 | 88.4 |
No | 43 | 11.6 |
Tachypnoea | ||
Yes | 306 | 82.5 |
No | 65 | 17.5 |
Chest distress | ||
Yes | 60 | 16.2 |
No | 311 | 83.8 |
Myalgia | ||
Yes | 122 | 32.9 |
No | 249 | 67.1 |
Headache | ||
Yes | 123 | 33.2 |
No | 248 | 66.8 |
Vomitus | ||
Yes | 74 | 19.9 |
No | 297 | 80.1 |
Diarrhoea | ||
Yes | 35 | 9.4 |
No | 336 | 90.6 |
Diabetes mellitus | ||
Yes | 92 | 24.8 |
No | 279 | 75.2 |
Immunodeficiency | ||
Yes | 1 | 0.3 |
No | 370 | 99.7 |
Hypertension | ||
Yes | 92 | 24.8 |
No | 729 | 75.2 |
Pregnancy | ||
Yes | 58 | 15.6 |
No | 313 | 84.4 |
Comorbidity | ||
Yes | 208 | 56.1 |
No | 163 | 43.9 |
Note. N: frequency, SD: standard deviation, RR: respiratory rate, %: percentage.
The determinants of oxygen saturation and length of hospitalisation are described in Tables 2 and 3. The results indicated that participant who had vomitus, hypertension, and also tachypnoea were significantly reported decreasing oxygen saturation. From analysis, we also found that patient who had tachypnoea.
Regression analysis of oxygen saturation among COVID-19 patients (n=371).
Variable | M | SD | B | Standardised β | p-Value |
---|---|---|---|---|---|
Age | |||||
<30 years | 303 | 81.7 | −0.001 | −0.002 | 0.968 |
≥30 years | 68 | 18.3 | Ref | Ref | |
Wheezing | |||||
Yes | 29 | 7.8 | −1.25 | −0.09 | 0.132 |
No | 342 | 92.2 | Ref | Ref | |
Fever | |||||
Yes | 262 | 70.6 | −0.06 | −0.01 | 0.901 |
No | 109 | 29.4 | Ref | Ref | |
Chest distress | |||||
Yes | 60 | 16.2 | 0.55 | 0.05 | 0.383 |
No | 311 | 83.8 | Ref | Ref | |
Vomitus | |||||
Yes | 74 | 19.9 | −1.63 | −0.17 | 0.001 |
No | 297 | 80.1 | Ref | Ref | |
Diabetes mellitus | |||||
Yes | 92 | 24.8 | 0.22 | 0.02 | 0.710 |
No | 279 | 75.2 | Ref | Ref | |
Hypertension | |||||
Yes | 92 | 24.8 | −1.18 | −1.22 | 0.034 |
No | 279 | 75.2 | Ref | Ref | |
Pregnancy | |||||
Yes | 58 | 15.6 | 0.14 | 0.01 | 0.848 |
No | 312 | 84.1 | Ref | Ref | |
Comorbid | |||||
Yes | 208 | 56.1 | 0.08 | 0.01 | 0.884 |
No | 163 | 43.9 | Ref | Ref | |
Headache | |||||
Yes | 123 | 33.2 | 0.09 | 0.01 | 0.853 |
No | 248 | 66.8 | Ref | Ref | |
Haemoglobin | |||||
Abnormal | 166 | 44.7 | 0.04 | 0.02 | 0.641 |
Normal | 205 | 55.3 | Ref | Ref | |
D-dimer | |||||
Abnormal | 127 | 41.2 | 0.00 | −0.06 | 0.264 |
Normal | 181 | 58.8 | Ref | Ref | |
Blood glucose | |||||
Abnormal | 71 | 20.2 | −0.002 | −0.063 | 0.303 |
Normal | 281 | 79.8 | Ref | Ref | |
Tachypnoea | |||||
Abnormal | 359 | 96.8 | −0.28 | −0.26 | 0.000 |
Normal | 12 | 3.2 | Ref | Ref | |
HR | |||||
Abnormal | 76 | 20.5 | −0.03 | −0.08 | 0.118 |
Normal | 295 | 79.5 | Ref | Ref |
Note: M: mean, SD: standard deviation, B: beta, RR: respiratory rate, HR: heart rate.
Bold: Significant value.
Regression analysis of length of hospitalisation more than 14 days (n=371).
Variable | N | % | OR (95% CI) | SE | p-Value |
---|---|---|---|---|---|
Tachypnoea | 3.80 (1.11–13.0) | ||||
Yes | 306 | 82.5 | Ref | 0.63 | 0.033 |
No | 65 | 17.5 | |||
Headache | 1.23 (0.11–0.51) | ||||
Yes | 123 | 33.2 | Ref | 0.40 | 0.000 |
No | 248 | 66.8 | |||
Fever | 2.24 (1.07–4.68) | ||||
Yes | 262 | 70.6 | Ref | 0.38 | 0.032 |
No | 109 | 29.4 | |||
D-dimer | 1.00 (1.00–1.001) | ||||
Abnormal | 127 | 41.2 | Ref | 0.00 | 0.006 |
Normal | 181 | 58.8 | |||
Blood glucose | 1.00 (1.00–1.005) | ||||
Abnormal | 71 | 20.2 | Ref | 0.01 | 0.006 |
Normal | 281 | 79.8 | |||
HR | |||||
Abnormal | 76 | 20.5 | 0.58 (0.29–1.13) | 0.34 | 0.110 |
Normal | 295 | 79.5 | Ref | ||
Diabetes mellitus | 2.23 (1.08–4.61) | ||||
Yes | 92 | 24.8 | Ref | 0.37 | 0.030 |
No | 279 | 75.2 | |||
Pregnancy | |||||
Yes | 58 | 15.6 | 0.27 (0.06–1.21) | 0.77 | 0.088 |
No | 312 | 84.1 | Ref | ||
Comorbidity | |||||
Yes | 208 | 56.1 | 0.93 (0.43–1.93) | 0.40 | 0.847 |
No | 163 | 43.9 | Ref |
Note: N: total number, %: percentage, OR: odd ratio, SE: standard error, HR: heart rate.
Bold: Significant value.
In this study, tachypnoea has the strongest relationship with oxygen saturation and length of stay. This is in line with the previous study that revealed the manifestation of tachypnoea due to the distribution of the majority of Angiotensin-converting enzyme 2 (ACE2) receptors in lung epithelial cells, where then the SARS-CoV-2 virus enters and destroys the alveoli.7,8 T helper CD4 cells and T cytotoxic CD8 cells begin to be trapped in the lung tissues. These cells play a role in fighting off the viruses, but they also play a role in the inflammation and subsequent lung injuries.9
It is important to note that vomiting significantly predicted lowered oxygen saturation. This aligns with the previous study with 27 autopsy cases, stating that vomiting followed by inhalation of gastric contents into the bronchial tract may cause pulmonary inflammation.10 The severity of lung injury increases significantly with the large volume of gastric contents aspirated and the low potential hydrogen (PH) of gastric contents.11 Patients experiencing the aspiration of gastric contents may experience respiratory signs and symptoms, such as wheezing, coughing, dyspnoea, cyanosis, pulmonary oedema, and hypoxaemia, which may develop into severe ARDS.12
Our study also found that hypertension contributed to lowered oxygen saturation. This study also aligned with the previous study, revealing that COVID-19 patients who suffered from hypertension as comorbidity showed low oxygen saturation levels.13 The possible explanation for this is the Angiotensin-Converting Enzyme 2 (ACE2) receptor as the site of attachment for the SARS-CoV-2 virus on the cell surface to enter the cell.14,15 The ACE2 catalyses the conversion of angiotensin II (a vasoconstrictor peptide) to angiotensin 1–7 (a vasodilator). This can bring influence the occurrence of hypertension in COVID-19 patients.
In addition, our study has shown that dyspnoea, fever, and diabetes mellitus (DM) are prognostic factors for a more extended hospitalisation. This result is consistent with the previous study, claiming that patients with more severe symptoms tend to be hospitalised longer than patients with less severe symptoms of the same diagnosis.16 In COVID-19 cases, dyspnoea and fever are signs of pneumonia, which could be classified as moderate symptoms of COVID-19.17 Meanwhile, studies on immunity showed that poorly controlled diabetes could inhibit the lymphocyte response and impair the function of monocytes, macrophages, and neutrophils,18,19 which means a longer hospitalisation.
Finally, this study shows that high D-Dimer also influences the length of hospitalisation. An increase in D-Dimer is a sign of coagulopathy, indicating that severe sepsis has occurred, leading to a critical illness.20 This suggests that the D-Dimer level is related to the disease severity, which has also been proven in a previous study describing that the D-Dimer level at admission is a risk factor for severe symptoms and death.6
This study had some limitations. First, our study recruits participants from one hospital, so the generalisation is low. Future study needs to include multiple centres and locations. Second, the causal relationship was difficult to build since we used a cross-sectional design. Longitudinal studies are required to explore the changes in oxygen saturation among COVID-19 patients. This study indicates important variables associated with oxygen saturation, including tachypnoea, vomiting, and hypertension. Health professionals should consider some variables, including dyspnoea, headache, fever, D-dimer, blood glucose, and diabetes mellitus, in reducing the length of hospitalisation of COVID-19 patients.
FundingThis research received no funding.
Conflict of interestThe authors declare no conflict of interest.
We thank Douglas S Umboh, MD, Director of Hermina Mekarsari Hospital, for the permission in conducting this research.
Peer-review under the responsibility of the scientific committee of “The 4th Udayana International Nursing Conference (4th INC)”. Full text and its content are under the responsibility of the authors of the article.