By Owhonda G; Nnoka VN;
Eli S; Ikenga VO; Wekere
FCC; Emeghara GI; Tee GP (2022).
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Greener
Journal of Medical Sciences Vol. 12(1),
pp. 116-122, 2022 ISSN:
2276-7797 Copyright
©2022, the copyright of this article is retained by the author(s) |
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Prevalence of COVID–19/HIV-Positive Patients
in an Isolation Center in Rivers State, Southern Nigeria.
Owhonda
G1; Nnoka VN2; Eli S3;
Ikenga VO4; Wekere
FCC1; Emeghara GI5; Tee GP5
Department of
community Medicine, Rivers State University.1
Department of
Pharmacology, Rivers State University.2
Mother, Baby and
Adolescent Care Global Foundation.3
Department of
Surgery, Rivers State University.4
Department of Human
Physiology, Rivers State University.5
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ARTICLE INFO |
ABSTRACT |
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Article No.: 030922032 Type: Research |
Background: COVID – 19 Infection/Human immunodeficiency Virus (HIV) co–infection is a double tragedy to those infected global.
The reason is that those infected with HIV have reduced immunity and at
greater risk of contacting COVID –19 infection
resulting in higher mortality. The global prevalence of COVID-19 infected
persons in people living with HIV (PLHIV) is 2%. Aim: This study aims to determine the prevalence of admitted patients with
COVID-19/HIV co-infection in an isolation center in
Rivers State, South-South region of Nigeria. Method: This was a 6 – months
cross-sectional study of COVID – 19/HIV- positive patients at an isolation
centre in Rivers State, Southern Nigeria. Polymerase Chain Reaction Test
(PCR) was used to confirm those that were COVID-19 positive and HIV.
Permission for the study was granted by the Director of Public Health, Rivers
State Ministry of Health. The data was analysed with SPSS version 25. Result: Three hundred and thirty five patients were recruited for the study
all of which were COVID-19 positive. There were 105 (44.7) males and 130
(55.3) females. The mean age was 38.4 SD 13.2 and .231(98.3) HIV positive. There were 1Male positive for HIV and 3
Females positive for HIV. Conclusion: The study revealed the prevalence of COVID – 19/HIV co-infection as
1.7%. Multi-disciplinary management should be instituted for better outcome.
In addition, residents should be encouraged to accept COVID-19 vaccination
for improved prognosis for those COVID – 19/HIV co-infection. |
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Accepted: 09/03/2022 Published: 25/03/2022 |
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*Corresponding Author Dr. Nnoka
V. (MBBS) E-mail: nnokaalentine@ yahoo.com Phone:
08064843958 |
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Keywords: |
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INTRODUCTION
Consequent on the COVID-19
pandemic, there have been fears over the increased susceptibility to severe
COVID-19 disease in people living with HIV (PLHIV) due to varying degrees of
immunosuppression1. Individuals with HIV infection who are not on
ARV medications are said to be at even greater risk. However, when compared
with other comorbidities like obesity, older age, severe asthma, diabetes
mellitus, heart or respiratory diseases, HIV appears to be a lower risk factor
for severe COVID-19 disease. People living with HIV who also have a heart or
respiratory disease or who are elderly are also more likely to acquire COVID-19
with greater severity of the disease compared with those without these
comorbidities (UNAIDS).2
This study aims to
determine the prevalence of admitted patients with COVID-19/HIV co-infection in
an isolation center in Rivers State, South-South region of Nigeria. According
to the National Agency for the Control of AIDS (NACA), Nigeria has a HIV
prevalent rate of 1.4% while Rivers State has a HIV prevalence rate of 3.8%
making it the 3rd highest among all the states in the country3.
CORONA
VIRUS DISEASE, 2019 (COVID-19).
Corona virus disease 2019
(COVID-19) is a disease that can be transmitted from person to person via inhalation
of contaminated air droplets containing the virus and whose etiology is the
severe acute respiratory syndrome coronavirus 2 (SARS CoV-2), a novel virus. In
December, 2019, the first known case of this disease was identified in Wuhan,
China4. Since then, the coronavirus disease has resulted in a
pandemic as almost all countries of the world have been affected one way or the
other5.
When the virus was first
identified in Wuhan, it was called the Wuhan coronavirus6. Since the
new 2015 World Health Organization (WHO) guidelines avoids naming diseases
according to geographical locations, or the group of people involved, so as to
avoid stigmatization7, the virus was officially named SARS-CoV-2 and
COVID-19 by the WHO in February, 20208. CO represents corona, VI
stands for virus, D stood for disease while 19 stands for the year the virus
was discovered being 20199.
As at the 10th
of February, 2022, there has being a total of 402,044,502 confirmed coronavirus
cases with about 5,770,023 related deaths worldwide8.
In Nigeria, as at 11th
of February, 2022, there has being a total of 253,923 confirmed cases with
3,139 COVID-19 related deaths. Out of this figures,
Rivers State with a population of over 5,198,716 (2006 census) has had about
16,499 confirmed cases with a total of 154 corona virus related deaths10.
Signs and
Symptoms
Symptoms may vary from
asymptomatic infection to mild, moderate or severe. They may include any
combination of fever, cough, catarrh, muscle or joint pain, fatigue, loss of
smell, loss of taste, headache, and difficulty in breathing. Shock, respiratory
failure or multi organ dysfunction can also occur. About 81% of symptomatic
persons develop only mild to moderate symptoms; only about 14% end up with
severe symptoms like difficulty in breathing while only 5% suffer from life
threatening symptoms like shock, respiratory collapse or multiorgan
failure. Time of exposure to symptom onset is usually between 4-5days on the
average11.
Pathophysiology
The virus first enters the
host through the target host cell receptor. SARS-CoV-2 is primarily made up of
four structural glycoproteins namely spike, envelop, membrane and nucleocapsid12.
Several works have been published all pointing to human angiotensin converting
enzyme 2 (ACE2) as a receptor that allows the entry of SARS-CoV-213,14. Apart from the lungs, ACE2 can also be expressed
in the small intestine, heart, testis, kidneys, adipose tissue and thyroid
gland which may mean that in conditions of a high viral load, SARS-CoV2 could
also infect cells of other organ system.2-4 The
virus enters the host cell through binding of the viral and host cell membrane.1-3
Host Defense
against SARS-CoV-2
In the initial phase of
infection, lung cells, epithelial cells of the bronchi and nasal cavity are
targeted by Corona virus with the aid of its spike protein which attaches to
ACE215. Uptake of the virus is enhanced by trans-membrane serene
protease 2 (TMPRSS2) which is present in the host cell. This is achieved via
the cleavage of ACE2 and the activation of the viral spike protein which is
responsible for the COVID-19 viral entry into the cells of the host15,16. As it is with some other viruses that affects the
respiratory system, TMPRSS2 and ACE2 are expressed in cells like the alveolar
epithelial type 2 pneumocytes17. Marked depletion of lymphocytes may
result from COVID-19 infection following destruction of T-cells18.
This could also result from inflammatory responses elicited by the virus (both
natural and acquired immune responses) which hampers the formation of
lymphocytes and promotes the programmed cell death of lymphocytes15,18.
Following continuous
replication of the virus in the later phase of the infection, the integrity of
the epithelial barrier is compromised19. COVID-19 attacks the
capillary endothelial cells of the lungs, enhancing the inflammatory response
with entry of neutrophils and monocytes. Viral sepsis can ensue leading to
multi-organ failure15,20.
Diagnosis and
laboratory findings
A provisional diagnosis of
SARS-CoV-2 can be made using symptoms alone, however,
this will have to be confirmed with the help of a reverse transcription
polymerase chain reaction (RT-PCR) of secretions containing the virus or some
other forms of nucleic acid testing21. Laboratory investigations
like a full blood count (FBC), C-reactive protein (CRP) radiological
investigations like chest radiographs, CT scans of the chest can also aid
diagnosis especially in individuals with a high index of suspicion22.
Laboratory findings may include
an increase in lactate dehydrogenase, alanine amino-transferase,
aspartate amino transaminase and C-reactive protein15. A decrease in
the number of Lymphocyte count (absolute lymphocyte count ˂ 1.0 × 10⁹/L)
is also a very common finding15,17.
Clinical
management and Treatment
Management of COVID-19
infection includes prevention and control of infection, supportive measures
like oxygen supplementation and mechanical ventilation as indicated (CDC).
New drugs have being developed
for the treatment of COVID-19 infection while there has been evaluation of some
already existing drugs. For example, Remdesivir is a
drug that has been approved by the U.S Food and Drug Administration for the
treatment of COVID-19 infection.
Chloroquine/hydroxychloroquine
compounds have previously been used to treat SARS-CoV-2 patients as this drug
inhibit entry of the virus into host cell and also cause endocytosis of the
virus invitro; however studies have not shown much
benefits15,23.
Dexamethaxone and statins
(anti-inflammatory agents) are other drugs that have reduced hospital stay and
severity of symptoms in patients with SARS-CoV-215.
Monoclonal antibodies that targets any of interleukin-1, interferon
gamma, or interleukin-6 serves as anti-inflammatory agents, preventing organ
damage in SARS-CoV-2 infection.
Immunomodulatory
therapies like Anakira, Ruxolitinib
and anti-coagulants like heparin have been tried with varying efficacies15.
Prevention
COVID-19 Preventive measures include
wearing of face mask, social distancing, reduction in outdoor exposures,
regular washing of hands with soap and water, use of hand sanitizers, avoiding
contact with the eyes, mouth or nose, respiratory etiquette and vaccination24.
Human
immunodeficiency virus
Human Immunodeficiency
virus (HIV) is a blood borne virus of the Retroviridae
family and Lentivirus
genus. The virus is said to have originated in Central Africa from chimpanzee25.
HIV has slowly spread across Africa and into other parts of the world. In the
long run, HIV can cause acquired immunodeficiency syndrome (AIDS) which is
characterized by depression of the immune system which makes way for
opportunistic infections and certain cancers26.
According to the W.H.O,
prior to 2021, there were about 37.7 million people infected with HIV worldwide
and over two thirds are within the African continent. In 2020 alone, not less
than 680,000 lost their lives following HIV-related causes with about 1.5
million new cases (WHO)27.
There are two species of
HIV – HIV-1 and HIV-2, each one containing several subtypes. HIV is usually
transmitted through sexual intercourse, sharing of needles and sharps, infected
blood and blood products, mother to child transmission (MTCT) which can occur
during the process of delivery or breastfeeding.
Pathophysiology
HIV infects cells that
participate in immune functions such as the T lymphocytes especially the CD4 T
cells, dendritic cells and macrophages28. As a result of the
infection with the virus, CD4 T cells are depleted by a number of ways
including but not limited to direct destruction by CD8 cytotoxic cells of CD4 T
cells that has been infected, apoptosis of bystander cells that are uninfected
etc29,30. Following the depletion of CD4 T
lymphocytes, a threshold level will be reached when cell mediated immunity will
be lost with antecedent susceptibility of the host to various types of
opportunistic infections eventually giving rise to full blown AIDS.
Diagnosis
An initial diagnosis of HIV
can be made using an enzyme-linked immunosorbent
assay (ELISA) which can be confirmed using any of western blot technique, Immunoflorescence assay (IFA) or a polymerase chain
reaction (PCR).
Signs and
symptoms
The signs and symptoms of
HIV infection depends on the stage of the disease. In the early phase of
infection, there could be seroconversion (typically
within the first 2-4 weeks of infection) which presents with flu-like symptoms
like fever, chills, generalized rashes, malaise, muscle aches, generalized
lymphadenopathy.
Acquired immunodeficiency
syndrome (AIDS) presents as a severe, recurrent and sometimes lethal
opportunistic infections and malignancies.
Treatment
At present, there is no
cure for HIV infection and current treatment modalities only aims to suppress
replication of the virus within the host allowing the individuals immune system
to recover and resume its role in the fight against opportunistic infections
and certain cancers27.
Current treatment regimen
consists of a combination of three or more antiretroviral (ARV) drugs.
Prevention
Preventive measures of HIV
infection includes use of condoms, routine screening for HIV and other sexually
transmitted diseases, prevention of mother to child transmission (MTCT) of HIV,
Post exposure prophylaxis (PEP) with ARV.
COVID-19 and
HIV co-infection
Consequent on the COVID-19
pandemic, there have been fears over the increased susceptibility to severe
COVID-19 disease in people living with HIV (PLHIV) due to varying degrees of
immunosuppression27. Individuals with HIV infection who are not on
ARV medications are said to be at even greater risk. However, when compared
with other comorbidities like obesity, older age, severe asthma, diabetes
mellitus, heart or respiratory diseases, HIV appears to be a lower risk factor
for severe COVID-19 disease. People living with HIV who also have a heart or
respiratory disease or who are elderly are also more likely to acquire COVID-19
with greater severity of the disease compared with those without these
comorbidities (UNAIDS). A study by Karmen-Tuohy et al
(2020) showed that HIV/COVID-19 co-infection does not have any significant
impact on the duration of hospital stay, presentation or outcome when compared
with individuals who are negative to HIV31. This was supported by
another work done by Nagarakanti et al (2021) which
also showed no difference in admission into the intensive care unit, need for
mechanical ventilation or even mortality amongst individuals with HIV/COVID-19
co-infection (who were on admission) when compared with COVID-19 positive
individuals without HIV infection32.
It is pertinent that people living with HIV adhere strictly to all the
preventive measures that have been put in place by the World Health
Organization (WHO) in other to avoid acquiring the SARS-CoV-2.
Aim
To
determine the prevalence of HIV infection amongst COVID - 19 positive patients
at an isolation centre in, Southern Nigeria.
METHODOLOGY
This was a 6 – months cross-sectional study of
HIV- COVID – 19 positive patients at an isolation centre
in Rivers State, Southern Nigeria. HIV confirmatory kit was used to confirm
those that were positive for HIV. Polymerase Chain Reaction Test was used to
confirm those that were COVID-19 positive. Permission for the study was granted
by the Director of Public Health, Rivers State Ministry of Health. The
information was analysed using SPSS version 25.
RESULT
Table 1: COVID-19 and HIV Co-Infection
|
Variable
|
Number
|
Percentage
|
|
Sex |
|
|
|
Female Male |
105 130 |
44.7 55.3 |
|
Age |
|
|
|
Mean
38.4 |
SD
13.2 |
|
|
Result
(HIV) |
|
|
|
Negative Positive
|
231 4 |
98.3 1.7 |
|
|
|
|
Mean
age 38±13.2
Table 2: Prevalence of HIV Among COVID – 19 Patients (COVID – 19/HIV Co-Infection)
|
|
RESULT |
Total |
|
|
SEX |
NEGATIVE
(%) |
POSITIVE |
|
|
Male
|
129
(99.2) |
1(0.8) |
130 |
|
Female |
102
(97.1) |
3(2.9) |
105 |
|
Total |
231
(98.3) |
4(1.7) |
235 |

Bar Chart of Male and Female
Distribution of HIV- Positive Infections
DISCUSSION
Our study revealed the
prevalence of HIV amongst COVID – 19 patients in an isolation center In southern Nigeria was 1.7% (table 1 and 2). This figure
was lower than the global figure of 2%.33 In
the study conducted by Tope Oyelade et al. 33. The
study showed that CIOVID – 19/ HIV Co – infection was highest amongst African
population .33 furthermore, the study revealed that HIV infection
may be linked with increased COVID – 19 death.
In the research carried out
by Algatitan JS et al in Spain showed that people
living with HIV are most affected by COVID – 19 infection.
34 In addition, the researchers showed that people giving with HIV
were feeling threatened with high level of fear, anxiety and stress because of
the possibility of being infected with another virus that could kill them.
Although there are ongoing research about COVID – 19 / HIV Co – infection much
is still unknown however early data revealed that people with HIV with a CD4
cell counts above 200 have the same risk for severe COVID – 19 as people
without HIV. 34 - 36 However in, persons with
HIV who have weaker immunity and are theoretically more vulnerable especially
the elderly and with poorer health. 3,7 It is combination of these variables age as
immunity in HIV positive patients with COVID – 19 that put them at greater
risk. 34 for this reason it is important that people with HIV have
adequate information, should not panic nor be over confident and should engage
in positive health behavior especially optimal adherence to treatment. 35
Our study showed that female
infected with COVID – 19 / HIV co – infection when compared to males in the
ratio 3 : 1; indicating that out of the
231 infected cases 3(2.9%) of the females had COVID – 19 / HIV co –infection compared to 1 (0.8%) males.
This was not actually in agreement
with some studies which revealed that there is inconclusive studies or hypothesis
whether females or males were more predisposed to COVID – 19/ HIV co-infection.
33
CONCLUSION
The study revealed the prevalence of
COVID – 19/HIV co-infection as 1.7%. Multi-disciplinary management should be
instituted for better outcome. In addition, residents should be encouraged to
accept COVID-19 vaccination for improved prognosis for those COVID – 19/HIV
co-infection.
Funding:
There was no funding for the research
work.
Ethical
Consideration:
Permission for the study was granted
from data collected by the office of the Director Public Health Department
Rivers State Ministry of Health, Nigeria.
REFERENCES
1. Mirzaei H, McFarland W, Karamouzian
M and Sharifi H (2020). COVID-19 among people living
with HIV: A systematic review. AIDS Behav. 1-8. doi: 10.1007/s10461-020-02983-2
2.
United States Agency for International Development (USAID).
https://www.unaids.org/en/covid19
3.
National Agency for the Control of AIDS (NACA), 2019. Nigeria
prevalence rate. https://www.naca.gov.ng/nigeria-prevalence-rate/
4. Page J, Hinshaw D and McKay B (2021). "In Hunt for Covid-19
Origin, Patient Zero Points to Second Wuhan Market – The man with the first
confirmed infection of the new coronavirus told the WHO team that his parents
had shopped there". The Wall Street Journal.
5. Zimmer C
(2021). "The Secret Life of a Coronavirus – An oily, 100-nanometer-wide
bubble of genes has killed more than two million people and reshaped the world.
Scientists don't quite know what to make of it". The New
York Times.
6. McNeil Jr DG (2020). "Wuhan Coronavirus Looks
Increasingly Like a Pandemic, Experts Say". The
New York Times. ISSN 0362-4331.
7. World
Health Organization (WHO), 2015. World Health Organization Best Practices for
the Naming of New Human Infectious Diseases (PDF) (Report). hdl:10665/163636.
8. World
Health Organization (WHO), 2020. Novel Coronavirus
(2019-nCoV) Situation Report – 1" (PDF).
9.
Coronavirus disease 2019 (COVID-19) in the EU/EEA and UK – eight update (PDF)
(Report). ecdc. Archived
(PDF) from the original on 14 March 2020. Retrieved 19 April, 2020
10. Nigeria
COVID-19 update (2021).Nigerian Center for Disease
Control (NCDC). https://covid19.ncdc.gov.ng/
11. Gandhi
RT, Lynch JB, and Del Rio C (2020). "Mild or Moderate
Covid-19". The New England Journal of Medicine.
383 (18): 1757–1766. doi:10.1056/NEJMcp2009249. PMID
32329974
12. Bohn MK,
Lippi G, Horvath A, Sethi S, Koch D, Ferrari M, Wang
C-B, Mancini N, Steele S and Adeli K (2020).
Molecular, serological, and biochemical diagnosis and monitoring of COVID-19:
IFCC taskforce evaluation of the latest evidence. Clin
Chem Lab Med 58: 1037–1052. doi:10.1515/cclm-2020-0722.
13. Letko M, Marzi A, and Munster V
(2020). Functional assessment of cell entry and receptor
usage for SARS-CoV-2 and other lineage B betacoronaviruses.
Nat Microbiol, 5: 562–569. doi:10.1038/s41564-020-0688-y.
14. Ou X, Liu Y, Lei X, Li P, Mi D, Ren L, Guo L, Guo
R, Chen T, Hu J, Xiang Z, Mu Z, Chen X, Chen J, Hu K, Jin Q, Wang J and Qian Z (2020). Characterization of spike
glycoprotein of SARS-CoV-2 on virus entry and its immune cross-reactivity with
SARS-CoV. Nat Commun,
11: 1620. doi:10.1038/s41467-020-15562-9.
15. Eli S, Orluwene CG, Oku IY, Bob-Manuel M, Enyinnaya
SO, Iyama AC, Nnoka VN and Emeghara GI (2022). Proposed treatment of
COVID-19 infection in a poor resource setting – the use of medicinal extract
from sunflower seed (Helianthus annuus seed).
IJSRA, 05(01), 009-015.
16. Zou X, Chen K, Zou J, Han P,Hao J and Han Z (2020).
Single-cell RNA-seq data analysis in the receptor
ACE2 expression reveals the potential risk of different human organs vulnerable
to 2019-nCOV infection. Front Med;14(2):185-192.
17. Garg S, et al. Clinical trends among US hospitalized with
COVID – 19. Ann Intern Med; 174(10): 1409-1419. Doi:
10.7326/M21-1991.
18. Mikami T, Miyashite H, Yanid T, et al (2021). Risk factors for
mortality in patients with COVID – 19 in New York City. J GEN INTERN
MED; 16:17-26.
19. Amakura Y, Yoshimura M, Yamakami
S, and Yoshida T (2013). Isolation of phenolic constituents and characterization
of antioxidant makers from sunflower (Helianthus annuus
L.) seed extract. Phytochemistry Letters; 6(2): 302 –
305.
20. Kamal J
(2011). Quantification of alkaloids, phenols, and flavonoids
in sunflower (Helianthus annuus L.).
Department of Biotechnology; 10(916): 3149 – 3151
21. Li MY, Li
L, Zhang Y and Wang XS (2020). Expression of the SARS-CoV-2
cell receptor gene ACE2 in a wide variety of human tissues. Infect Dis
Poverty 9: 45. doi:10.1186/s40249-020-00662-x.
22. Salehi S, Abedi A, Balakrishnan S, and Gholamrezanezhad
A (2020). "Coronavirus Disease 2019 (COVID-19): A Systematic Review of
Imaging Findings in 919 Patients". AJR. American Journal of Roentgenology.
215 (1): 87–93. doi:10.2214/AJR.20.23034.
23. Whigham LD, Watras AC and Schoeller DA (2007). Efficacy of conjugated linoleic acid
for reducing fat mass: a meta – analysis in humans;
American Journal of Clinical Nutrition; 85(5):1203 – 1211.
24. Centers
for Disease Control and Prevention (2020). www.cdc.gov/media/releases/2020/archives.html
25.
Gao F, Bailes E, Robertson D.L et
al. (1999). Origin of HIV-1 in the chimpanzee pan troglodytes
troglodytes. Nature, 397(6718):436-41.
26. Powell
MK, Benková K, Selinger P, Dogoši M, Kinkorová Luňáčková I, Koutníková
H, Laštíková J, Roubíčková
A, Špůrková Z, Laclová
L, Eis V, Šach J and Heneberg P (2016). "Opportunistic Infections in
HIV-Infected Patients Differ Strongly in Frequencies and Spectra between
Patients with Low CD4+ Cell Counts Examined Postmortem and Compensated Patients
Examined Antemortem Irrespective of the HAART
Era". PLOS ONE. 11 (9)
doi:10.1371/journal.pone.0162704
27. World
Health Organization (2021). HIV/AIDS.
https://www.who.int/news-room/fact-sheets/detail/hiv-aids
28.
Cunningham AL, Donaghy H, Harman AN, Kim M and Turville SG (2010). "Manipulation of
dendritic cell function by viruses". Current
Opinion in Microbiology. 13 (4): 524–9. doi:10.1016/j.mib.2010.06.002.
29. Garg H, Mohl J and Joshi A
(2012). "HIV-1 induced bystander apoptosis". Viruses.
4 (11): 3020–43. doi:10.3390/v4113020
30. Kumar V
(2012). Robbins Basic Pathology (9th ed.). p. 147. ISBN 978-1-4557-3787-1.
31. Karmen-Tuohy S, Carlucci P.M, Zervou
F.N, Zacharioudakis I.M, Rebick
G, Klein E, Reich J, Jones S, and Rahimian J (2020).
Outcomes among HIV-Positive patients hospitalized with COVID-19. J Acquir Immune Defic Syndr; 85(1):6-10. DOI;
10.1097/QAI.0000000000002423.
32. Nagarakanti S.R, Okoh A.K and Bishburg E (2021). Clinical outcomes of
patients with COVID-19 and HIV coinfection. J
Med Virol, 93(3): 1687-1693. DOI: 10.1002/jmv.26533.
33. Oyelade T, Algaltani JS, Hjazi AM, Li A, Kamila A; Raya R P. Global and Regional Prevalence and Outcomes
of COVID – 19 in people living with HIV: A Systematic Review and Meta –
Analysis. Trop Med. Infect Dis. 2022 3; 7 (2): 22.
34. Algatitan JS, Aldhahiv AM, Oyelade T, Alghamdi
SM, Almamary AS.
Smoking Cessation during COVID - 19. The top to – do list. Prim. Care
Respire. Med 2021; 31: 1-3.
35. Yang J, Zheng Y, Guox, Puk, Chen Z, Guo Q, JiR, Wang Y Zhon Y. Prevalence of
Comorbidities in the Novel Wuhan Coronanrns (Covid – 19) infection: A Systematic Review and Meta –
Analysis, Int. J Infect. Dis 2020: 94: 91-95.
36. Seyed Alinghi S, et al.
Prevalence of Covid – 19 like Symptoms among people
living with HIV and using Anti Retroviral Therapy
for Preventing ad Treatment. Curr HIV Resp. 2020; 18(5): 373 – 380.
37. Shekhar R.et al. Coronavirus Disease of 2019 in patients
with well – Controlled Human Immunodeficiency Virus on Antiretroviral Therapy.
J Acquire Immune Defic Syn
2020; 85 (1): e1 – e4.
38. Seyed Alirighi et al. Prevalence of Covid
– 19 like Symptoms among People Living with HIV, and using Antiretroviral
Therapy fo Prevention and Treatment Curr HIV Res 2020; 18 (5): 373 – 380.
39. The Virus
That Changed Spain. Impact of COVID – 19 on people with HIV. Ballester – Amal. R, Gil –llaria M. Https://www.ncbi:nlm.nlm.Gov (accessed 9/3/2022)
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Cite this Article: Owhonda G; Nnoka
VN; Eli S; Ikenga VO; Wekere
FCC; Emeghara GI; Tee GP (2022). Prevalence of
COVID–19/HIV-Positive Patients in an Isolation Center in Rivers State,
Southern Nigeria. Greener Journal of
Medical Sciences, 12(1): 116-122. |