|Year : 2013 | Volume
| Issue : 1 | Page : 10-16
The potential anesthetic threats, challenges and intensive care considerations in patients with HIV infection
Sukhminder Jit Singh Bajwa, Ashish Kulshrestha
Department of Anaesthesiology and Intensive Care, Gian Sagar Medical College and Hospital, Ram Nagar, Banur, Punjab, India
|Date of Submission||14-Jan-2012|
|Date of Decision||20-Jun-2012|
|Date of Acceptance||07-Aug-2012|
|Date of Web Publication||28-Jan-2013|
Sukhminder Jit Singh Bajwa
Department of Anaesthesiology and Intensive Care, Gian Sagar Medical College and Hospital, Ram Nagar, Banur, Punjab
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Acquired immunodeficiency syndrome (AIDS) has become a pandemic with ever looming danger of its transmission in health professionals. The number of AIDS patients has increased tremendously over the last two decades, who present for surgical procedures as well as who get admitted in intensive care unit for their critical condition. As such anesthesiologists and intensivists are exposed to potential risk of disease transmission on a daily basis from such patients. The guidelines and protocols formulated in the western world regarding prevention of disease transmission cannot be applied uniformly in the developing nations, such as India due to various factors and limitations. As such there is a continuous need felt in this arena to prevent the catastrophic consequences of AIDS in our medical fraternity while treating such patients in operation theatres and critical care units. This study reviews the various pathophysiological aspects, anesthetic considerations, intensive care implications, and various areas where current knowledge about AIDS can be applied to prevent its potential transmission in high-risk clinical groups.
Keywords: Acquired immunodeficiency syndrome, anesthesia, anti-retroviral therapy, human immunodeficiency virus, intensive care
|How to cite this article:|
Bajwa SS, Kulshrestha A. The potential anesthetic threats, challenges and intensive care considerations in patients with HIV infection. J Pharm Bioall Sci 2013;5:10-6
|How to cite this URL:|
Bajwa SS, Kulshrestha A. The potential anesthetic threats, challenges and intensive care considerations in patients with HIV infection. J Pharm Bioall Sci [serial online] 2013 [cited 2018 Aug 16];5:10-6. Available from: http://www.jpbsonline.org/text.asp?2013/5/1/10/106554
Acquired immunodeficiency syndrome (AIDS) was first described in 1981 in adults and the causative agent was first isolated in 1983. , According to the United Nations report on AIDS in 2007, about 33 million people were living with human immunodeficiency virus (HIV) and around 2.7 million were newly infected.  Developing nations like India has about 2.5 million people infected with the virus.  As a result this pandemic of AIDS has engulfed the entire globe in its grip.
The medical fraternity is at the highest risk among various professions as they are invariably and frequently exposed to established and undiagnosed cases of AIDS. Anesthesiologist' services are frequently sought either for any elective/emergency surgery or during the care of critically ill patients in intensive care unit (ICU). Though in established cases of AIDS, precautions can be taken but many a time during emergency situations and mass casualties, large numbers of patients are encountered. The potential risk of HIV transmission during these circumstances increases manifold from undiagnosed and unsuspected positive HIV cases. These risks certainly increase during the performance of invasive procedures such as intubation and airway management, securing of peripheral and central vascular access, insertion of Ryle's tube and urinary catheter. The risk increases further if the approach during these procedures is a casual one.
Tremendous advancement in understanding and management of this disease over the last decade has brought about prolongation of life span of the infected people. This subset of population can come for various types of elective or emergency surgeries, so the attending anesthesiologist is faced with managing these patients keeping in mind of various implications of this disease on anesthesia. An estimated 20-25% of all HIV infected patients come for various surgeries at some point of their lives. 
The causative agent is HIV belonging to the family retroviridae and subfamily lentivirus and is a single stranded RNA virus. , Two subtypes have been described: HIV 1 and 2. The pathogenesis involves binding of viral envelope protein GP160 to the specific CD4 receptors found on T4 lymphocytes (T-helper cells) of immune system. This process also requires a co-receptor named chemokine co-receptor (CCR5). After binding, the virion fuses with the host cell membrane and gets internalized. The viral RNA is then transcribed to host DNA by the enzyme reverse transcriptase present within the virion. This pro DNA is then integrated to the host DNA by the enzyme integrase. The viral DNA can remain integrated to the host DNA in an inactive form for many years. Once activated, the pro viral DNA transcribes viral RNA and messenger RNA which later forms various viral proteins forming viral progeny. Inhibition of viral replication is usually targeted by the various anti-retroviral agents. With the progress of the disease, the T-helper immune cells become deficient both quantitatively as well as qualitatively, leading to the opportunistic infections and neoplasms.
Classification of the disease
WHO and Centre for Disease Control and Prevention (CDC) have classified HIV infection according to the clinical symptoms and severity of immune suppression as depicted in [Table 1]. 
According to the World Health Organization, established HIV infections can be classified based on the CD4 cell counts which suggests the severity of immunological compromise and also can be used to know the effectiveness of anti-retroviral therapy. The classification is depicted in [Table 2].
| Pre-operative Anesthetic Considerations|| |
History and systemic examination
It has been observed and reported as well that during history taking only 20% of the physicians seek drug abuse history and much lesser than that enquire about the possibility of HIV infection.  Various systems may be involved due to direct consequence of opportunistic infections or neoplasms or may be due to other causes such as side-effects of anti-retro viral medications. Therefore, a detailed history encompassing physiological functioning of the individual organ system should be elicited.
Both the upper as well as lower respiratory tract may be involved due to opportunistic infections or neoplasms, e.g., Kaposi's sarcoma. Bronchitis, sinusitis, pneumonia caused by encapsulated bacteria like Haemophilus influenzae, Streptococcus pneumonia, etc., have been seen as well as infection with Mycobacterium tuberculosis n develop early in the course of disease. Atypical mycobacterium and fungal infections are also common in these patients especially with low CD4 T-cell counts. Pneumocystis carinii opportunistic pneumonia has been found in most of the patients and may be the earliest indication of the disease.
The cardiovascular system may be involved due to a primary HIV infection or due to the side-effects of anti-retroviral therapy. Pericardial effusion may arise due to infection itself, due to opportunistic infection or due to neoplasms. Dilated cardiomyopathy, known as HIV-associated cardiomyopathy, have been described as a late complication due to primary or secondary opportunistic infections or due to side-effects of anti-retroviral drugs like reverse transcriptase inhibitors, which causes mitochondrial toxicity. Acute coronary syndrome has been found in patients taking protease inhibitors more so in patients with pre-existing cardiovascular disease. Various auto-immune vasculitis like poly arteritis nodosa, Henoch-Schonlein purpura, Takayasu's arteritis and Kawasaki-like syndrome have been found in these patients. Recently, pulmonary arterial hypertension associated with HIV infection has also been described. 
Neurological abnormalities may develop in 90% of patients with HIV infection. Almost all the structures in nervous system may be involved, e.g., meninges, brain, spinal cord, peripheral nerves and muscles.  These include: Opportunistic infections, e.g., Cryptococcus, toxoplasma, aspergillus, candida, etc.
- Aseptic meningitis
- Subacute encephalitis
- Herpes simplex encephalitis
- Multifocal leukoencephalopathy
- Autonomic neuropathy
- HIV-related dementia and neurocognitive impairment.
Various hematologic abnormalities associated with HIV infection includes: 
These may be a result of direct HIV infection, secondary opportunistic infections or toxic effects of anti-retroviral drugs.  Hematologic malignancies have also been described.
- Coagulation abnormalities.
Involvement of renal system may be due to nephrotoxic effects of anti-retroviral drugs causing acute renal failure or due to chronic effects of HIV infection leading to end stage renal disease. Anesthetic technique has to be modified in these patients with renal involvement in accordance with the severity of the disease. ,
Involvement of oral cavity with lesions due to candida or infiltrative neoplasms can lead to dysphagia and odynophagia. These lesions can easily bleed during instrumentation of upper gastrointestinal tract as in Ryle's tube insertion or direct laryngoscopy. Chronic diarrhea due to infection with cytomegalovirus, cryptosporidium or other bacteria can cause severe fluid and electrolyte imbalances and should be evaluated pre-operatively.
Endocrine system and metabolism
Lipodystrophy and metabolic syndrome involving elevated plasma triglycerides, glucose and cholesterol have been found due to side-effects of anti-retroviral therapy. Other abnormalities may include:
- Adrenal insufficiency
- Syndrome of inappropriate secretion of anti-diuretic hormone (SIADH)
- Hypo- or hyperthyroidism
- Lactic acidosis due to side-effects of anti-retroviral drugs, e.g., nucleoside/nucleotide analogues.
| Laboratory Profile and Investigations|| |
A thorough pre-anesthetic evaluation should be supplemented with laboratory data in all HIV infected patients to know the severity of disease, organ systems involved and presence of other co-morbid illnesses which may have implications on anesthetic technique. A complete evaluation of anti-retroviral drugs should be made pre-operatively.  Laboratory investigations should include:
The overall risk of anesthesia and surgery in HIV infected patients is not documented but no elective surgery should be deferred on basis of HIV positivity alone.  The type of anesthetic technique used in HIV infected patients depends upon the type of surgery, severity of HIV infection and presence of co-morbid diseases. General anesthesia can safely be used in these patients but drug interactions and systems involved and their implications should be kept in mind. Drugs like etomidate, atracurium, remifentanyl, and desflurane can be safely used as their metabolism is independent of cytochrome 450 enzyme.
- Complete blood count with coagulation parameters, renal and hepatic function tests.
- Electrocardiogram (ECG) and Echocardiogram if ECG shows abnormality.
- Pulmonary function tests and arterial blood gas analysis to know severity of pulmonary system involvement.
- Chest X-ray if indicated.
- Advanced imaging modalities, e.g., CT scan, MRI, etc., to be done if clinical condition warrants.
Regional anesthesia can also be considered in less advanced disease with no neurological deficits or coagulation abnormalities. Central neuraxial blockade have been studied in obstetric anesthesia with no adverse effects provided no neurological deficits exist pre-operatively. ,,[16 ]
Combination therapy known as highly active anti-retroviral therapy (HAART), have undergone tremendous advancement in recent years. The drugs are classified according to the mechanism of inhibition of viral replication as shown in [Table 3]. 
Adverse drug effects
The side-effects associated with anti-retroviral drugs can be summarized as: 
- Mitochondrial dysfunction: Lactic acidosis, hepatotoxicity, pancreatitis, peripheral neuropathy.
- Metabolic: Lipodystrophy, hyperglycemia, body habitus changes, insulin resistance, osteoporosis.
- Bone marrow suppression: Pancytopenia.
- Allergi creactions: Skin rashes and hypersensitivity reactions.
Interaction of anti-retroviral drugs with anesthetic drugs and other agents are very important as these patients usually are on multiple drugs.  Pharmacodynamic interactions may be avoided by proper selection of anesthetic agents that have minimal effects on hepatic or renal systems. NRTI's have been implicated in causing lactic acidosis and hence long term propofol infusions should be avoided in such patients.
Pharmacokinetic interactions involves induction or inhibition of hepatic enzymes particularly CYP4503A4 enzyme. The various group of anesthetic drugs affected are:
Pre-operative anti-retroviral therapy
- Opioids: Ritonavir (PI) both induces and inhibits hepatic enzyme thus enhancing the effects of fentanyl by reducing the clearance and by increasing the active metabolites
- Benzodiazepines: Saquinavir (PI) inhibits midazolam metabolism
- Calcium channel blockers: Enzyme inhibition can enhance their hypotensive effect
- Neuromuscular blockers: Prolonged effects of muscle relaxants have been observed
- Local anesthetics: Plasma levels of lignocaine may be increased due to enzyme inhibition.
It is recommended to continue anti-retroviral therapy during pre-operative period to reduce drug resistance as long as it is compatible with the surgery. Only few anti-retroviral drugs, e.g., zidovudine, are available as parenteral preparations.
Anesthetic implications in obstetrical patients with HIV infection
Pregnancy in the setting of HIV infection has been the most debated topic among women of child bearing age and extensive research is being carried out throughout the globe. Anesthesiologists are also encountering increasing number of parturients some of them may be established cases while other gets diagnosed for the first time in the hospital setting.  As in other patients of HIV infection, patients' disease status and current treatment should be reviewed carefully. The minimum necessary investigations required in these cases include hemoglobin, blood count, coagulation profile, liver function tests, renal panel, ECG, roentgenogram and echocardiography.
Choice of anesthetic technique
There had been concerns of immune suppression with general anesthesia but nothing conclusive has been established till date. , However, the risk increases with administration of GA due to underlying pulmonary and cardiac pathology. Regional anesthesia had also been a subject of controversy due to claims of possible central nervous system involvement. , It has been now clearly established that neuraxial anesthesia can be administered safely in patients with HIV infection. , One of the chief concerns with this technique is the failure to treat the complications associated with post-dural puncture headache. 
The responsibility of anesthesiologist lies not solely in caring for the mother only but he has to take care of the neonate as well. Therefore, a judicious use of anesthetic drugs is warranted so as not to affect the neonatal apgar scores. The risk of transmission of HIV from mother to fetus is around 25% which can be reduced to 2% by combination of anti-retroviral therapy and elective caesarean section. ,,, There is very little literary evidence to suggest that HIV increases complications of pregnancy or pregnancy alters the HIV disease progression in a parturient.  The marked reduction in incidence of disease transmission should not be the sole criterion for subjecting the parturients to elective caesarean section (CS) as maternal mortality and morbidity increases with operative delivery as compared to normal vaginal delivery.  However, American college of obstetrics and gynecology (ACOG) has stated that an elective CS should be offered to every HIV infected parturient to reduce the risk of vertical transmission.
Challenges in critically ill patients with HIV infection
The HIV infected patients may require intensive care for variety of reasons which may be due to complications arising out of primary infection or may be due to other surgical or medical reasons unrelated to HIV infection. With the advancement in anti-retroviral therapy, the mortality in HIV infected patients requiring intensive care have been reduced from 70% in 1980s to 30-40% in 2002. 
Major causes necessitating ICU admission
The most common reason for ICU admission in HIV infected patients is acute respiratory failure and Pneumocystis carinii pneumonia (PCP) constitutes about 25-50% of these cases.  There has been an improvement in survival rates in PCP related acute respiratory failure from 0-13% in 1980s to about 30-45% in 1990s, which may be attributed to the advancement in anti-retroviral therapy, increased use of PCP prophylaxis and adjunctive corticosteroid treatment in moderate to severe PCP. Patients usually presents with fever, dry cough and shortness of breath followed by oxygen desaturation on exertion severe PCP manifests on chest X-ray as diffuse bilateral granular opacities with development of air containing pneumatoceles, predisposing to pneumothorax. Bronchoalveolar lavage cytology is the gold standard for diagnosing PCP. The important differential diagnoses involve disseminated infection with histoplasma, coccidiomyces and invasive aspergillusfumigatus infection. About 20% of PCP infections are complicated with concomitant bacterial infection. The need for mechanical ventilation and presence of pneumothorax are considered as poor prognostic indicators in patients with PCP infection. 
Therapy with high dose trimethoprim-sulfamethoxazole combination is the first line treatment but is often complicated by rash, neutropenia and fever. Pentamidine and clindamycin comes as second line of treatment whereas primaquine and combination of dapsone with trimethoprim is reserved for those intolerant to first and second line of treatment. High dose corticosteroids within 24-72 hours of PCP treatment initiation can be considered in hypoxemic patients as these have shown to reduce morbidity and mortality. 
The other causes of acute respiratory failure in HIV infected patients are bacterial pneumonias caused by Pseudomonas, Staphylococcus aureus, etc., which usually require antibacterial treatment. HIV-associated lymphocytic interstitial pneumonitis and bronchiolitis obliterans organizing pneumonia (BOOP) are some rare pathology which may be seen in these patients.
Opportunistic mycobacterium infection is also frequent in HIV positive patients and is usually seen in conjunction with extra-pulmonary manifestations. The Mycobacterium avium complex (MAC) is also common in developed countries and is seen in those with CD4 counts less than 50/μl.
The other common reason for intensive care admission in these patients may be neurological pathologies comprising up to 27% of admissions.  Cerebral toxoplasmosis is common in these patients and usually presents with focal neurological signs, fever, seizures and depressed consciousness. The diagnosis can be made by serum antibody testing and brain biopsy might be needed to differentiate it from other similar pathologies (cerebral abscess, tuberculoma, neurosyphilis and progressive multifocal leukoencephalopathy). The treatment includes sulfadiazine and pyrimethamine with high incidence of adverse drug reactions.
Another common infection seen in HIV-positive patients is cryptococcosis of central nervous system (CNS). It presents with non-specific symptoms of fever, headache and vomiting and the diagnosis is confirmed by demonstration of Cryptococci in cerebrospinal fluid on India ink staining. The treatment is usually with liposomal amphotericin B and flucytosine.
Other common CNS pathologies seen in these patients are non-Hodgkin's lymphoma, progressive leukoencephalopathy and HIV encephalopathy. Glasgow coma scale of less than 7 or signs of brainstem involvement at the time of intensive care admission are considered as independent predictors of mortality. 
Bleeding from gastrointestinal tract often due to ulcerations, Kaposi's sarcoma, lymphoma, gastric or duodenal ulcers, varietal bleeding, etc., may result in intensive care admissions. Bowel perforation secondary to cytomegalovirus enteritis, lymphomas, cholangiopathy and pancreatitis are other possible causes of intensive care admissions in these patients.
Severe sepsis accounts for approximately 15% of diagnoses in HIV-positive patients admitted to ICU with an increased mortality as compared to those without HIV/AIDS.  Patients should undergo aggressive management with appropriate antibiotics as mortality in these patients is high.
The introduction to highly active anti-retroviral therapy (HAART), classification, mechanism of action of various drugs and common adverse effects has already been dealt before. An important adverse effect of HAART especially seen in ICU patients known as immune reconstitution inflammatory syndrome needs to be mentioned here. It is a life threatening adverse reaction seen days to weeks after initiation of HAART and usually presents as paradoxical worsening of previous infection which is either partially treated or recently treated with concomitant worsening hypoxemia and an increase in chest infiltrates and adrenomegalies.  It is thought to result from an exuberant inflammatory response in presence of pathogens, e.g. M. avium complex. 
Mortality predictors in IC
The predictors of poor prognosis or higher mortality in these patients admitted in intensive care are sepsis, respiratory failure requiring mechanical ventilation, low serum albumin and a high acute physiology and chronic health evaluation II (APACHE II) score. The initiation of HAART for improving prognosis depends on the clinician assessment.
Risks and mechanisms of disease transmission
There always remains a high risk of HIV transmission in anesthetic practice. HIV infection can be transmitted from patient through sharp injuries, broken skin contact with body fluids and splashing of mucosal surfaces. The risk of transmission by needle stick injury may be between 0.03 and 0.3% depending on factors like hollow needle injury, volume of blood inoculated and depth of needle puncture. The possible risk of HIV transmission from patient to patient results from reuse of syringes, airway devices or respiratory circuits. Disposable circuits and use of hydrophobic filters should be instituted in an infected patient. Laryngoscopes should be properly sterilized before reuse. The risk of HIV transmission from anesthesiologist to patient is estimated at around 2.4-24 per million procedures.
All types of in hospital transmission of HIV infection can be effectively reduced by implementing 'Universal Precautions' which is defined by CDC as set of precautions designed to prevent transmission of HIV infection to health workers while providing health care.  It involves proper handling of blood, body fluids containing semen, blood, tissues, cerebrospinal fluid, pleural fluid, peritoneal, pericardial, and amniotic fluids. Various measures described are washing hands, wearing double gloves, eye protection, feet protection, proper handling of needles and sharps, and proper sterilization of instruments and linen.
The health workers are in a constant danger of exposure to an HIV infected patient as they are involved in the care of such patients. The need to start the post-exposure prophylaxis for these exposed health workers depends upon:
The need for post-exposure prophylaxis should be ascertained by a team of experts keeping in mind all the factors involved in transmission of disease and it should be started within 72 hours of exposure and can be continued for four weeks. The variousrecommendations for post-exposure prophylaxis are summarized in following table [Table 4]. ,
- Nature of inoculums, i.e., percutaneous or mucosal splash, large or small volume of blood and hollow or closed needle injuries.
- Patient's viremic status, i.e., HIV negative, unknown or HIV positive.
Basic two drug regimen: Zidovudine 600 mg/day in divided doses + Lamivudine 150 mg twice a day.
Expanded three drug regimens: Basic two drug regimen + one of the following:
Nevirapine (NNRTI) is usually not recommended for post-exposure prophylaxis.
- Indinavir 800 mg three times a day on an empty stomach.
- Nelfinavir 750 mg three times a day with meals.
- Efavirenz 600 mg once a day at bed time
- Abcavir 300 mg two times a day.
Post-exposure prophylaxis in pregnancy
If the pregnant female is exposed, the decision to initiate the therapy should be taken after thorough discussion and after weighing the potential risks and benefits to the mother and fetus. The following drugs should be avoided in pregnancy:
Blood transfusion and HIV
- Efavirenz due to its suspected teratogenicity in animals.
- Combination of stavudine and didanosine due to its potential to cause severe lactic acidosis.
- Indinavir due to the risk of hyperbilirubinemia in newborn.
Scientific data exists for the immunomodulatory effect of allogenic blood transfusion known as Transfusion Related Immunomodulation (TRIM).  It has been suggested that there is an increase in viral load in patients with advanced HIV infection with the use of blood transfusion and hence it should be used cautiously if need arise. 
Pain related to HIV infection
HIV infection is often accompanied with both acute and chronic pain whose etiology is multifactorial which includes opportunistic infections like herpes simplex, peripheral neuropathy, HIV related arthralgia or drug related pain. The pain associated with HIV infection is often debilitating and is mostly undertreated. The approach towards treatment of HIV related pain should be multidisciplinary and should be given equal importance as that of the treatment of HIV.
| Conclusions|| |
HIV infection has become a growing danger to the humanity and the anesthesiologist is often faced with difficulty in managing such patients for various surgeries. The anesthetic technique should be chosen keeping in mind various implications of this disease on the body. The care of such patients in intensive care also should be done with all the universal precautions to reduce the cross infection to health care personnel.
| References|| |
|1.||Gottlieb MS, Schroff R, Schanker HM, Weisman JD, Fan PT, Wolf RA, et al. Pneumocystis carinii pneumonia and mucosal candidiasis in previously healthy homosexual men: Evidence of a new acquired cellular immunodeficiency. N Engl J Med 1981;305:1425-31. |
|2.||Barré-Sinoussi F, Chermann JC, Rey F, Nugeyre MT, Chamaret S, Gruest J, et al. Isolation of a T-lymphotropic retrovirus from a patient at risk for acquired immune deficiency syndrome (AIDS). Science 1983;220:868-71. |
|3.||Bokazhanova A, Rutherford GW. The epidemiology of HIV and AIDS in the world. Coll Antropol. 2006;30 Suppl 2:3-10. |
|4.||Eichler A, Eiden U, Kessler P. Aids and anesthesia. Anaesthesist 2000;49:1006-17. |
|5.||Fauci AS, Lane HC. Human immunodeficiency virus disease: AIDS and related disorders. In: Fauci AS, Braunwald E, Kasper DL, Hauser SL, Longo DL, Jameson JL, editors. Harrison′s Principles of Internal Medicine. 17 th ed. New York: McGraw-Hill; 2008. p. 1137-204. |
|6.||Levy JA. Human immunodeficiency viruses and the pathogenesis of AIDS. JAMA 1989;261:2997-3006. |
|7.||World Health Organization. WHO case definitions of HIV for surveillance and revised clinical staging and immunological classification of HIV-related diseases in adults and children. 2007. |
|8.||Ogilvie G, Adsett S, Macdonald G. Do physicians discuss HIV testing during prenatal care? Can Fam Physician 1997;43:1376-81. |
|9.||Lederman MM, Sereni D, Simonneau G, Voelkel NF. Pulmonary arterial hypertension and its association with HIV infection: An overview. AIDS 2008;22 Suppl 3:S1-6. |
|10.||Leelanukrom R. Anaesthetic considerations of the HIV-infected patients. Curr Opin Anaesthesiol 2009;22:412-8. |
|11.||Hoffman RM, Currier JS. Management of antiretroviral treatment-related complications. Infect Dis Clin North Am 2007;21:103-32, i×. |
|12.||Weller IV, Williams IG. ABC of AIDS. Antiretroviral drugs. BMJ 2001;322:1410-2. |
|13.||Jones S, Schechter CB, Smith C, Rose DN. Is HIV infection a risk factor for complications of surgery? Mt Sinai J Med 2002;69:329-33. |
|14.||Avidan MS, Groves P, Blott M, Welch J, Leung T, Pozniak A, et al. Low complication rate associated with cesarean section under spinal anesthesia for HIV-1-infected women on antiretroviral therapy. Anesthesiology 2002;97:320-4. |
|15.||Kuczkowski KM. Human immunodeficiency virus in the parturient. J Clin Anesth 2003;15:224-33. |
|16.||Evron S, Glezerman M, Harow E, Sadan O, Ezri T. Human immunodeficiency virus: Anesthetic and obstetric considerations. Anesth Analg 2004;98:503-11. |
|17.||Hughes SC, Dailey PA. Human immunodeficiency virus in the delivery suite. In: Hughes SC, Levinson G, Rosen MA, editors. Shnider and Levinson′s Anesthesia for Obstetrics. 4 th ed. Philadelphia: Lippincot, Williams and Willkins; 2002. p. 583-95. |
|18.||Thomson DA. Anesthesia and the immune system. J Burn Care Rehabil 1987;8:483-7. |
|19.||Kanzer MD. Neuropathology of AIDS. Crit Rev Neurobiol 1990;5:313-62. |
|20.||Spector SA, Hsia K, Pratt D, Lathey J, McCutchan JA, Alcaraz JE, et al. Virologic markers of human immunodeficiency virus type 1 in cerebrospinal fluid. The HIV Neurobehavioral Research Center Group. J Infect Dis 1993;168:68-74. |
|21.||Bremerich DH, Ahr A, Büchner S, Hingott H, Kaufmann M, Faul-Burbes C, et al. Anesthetic regimen for HIV positive parturients undergoing elective cesarean section. Anaesthesist 2003;52:1124-31. |
|22.||Hughes SC, Dailey PA, Landers D, Dattel BJ, Crombleholme WR, Johnson JL. Parturients infected with human immunodeficiency virus and regional anesthesia. Clinical and immunologic response. Anesthesiology 1995;82:32-7. |
|23.||Loo CC, Dahlgren G, Irestedt L. Neurological complications in obstetric regional anesthesia. Int J Obstet Anesth 1994;7:167-9. |
|24.||European Mode of Delivery Collaboration. Elective caesarean-section versus vaginal delivery in prevention of vertical HIV-1 transmission: A randomised clinical trial. Lancet 1999;353:1035-9. |
|25.||International Perinatal HIV Group. The mode of delivery and the risks of vertical transmission of human immunodeficiency virus type-1: a meta-analysis of 15 prospective cohort studies. N Engl J Med 1999;340:977-87. |
|26.||Kuczkowski KM. Anesthetic considerations for the HIV-infected pregnant patient. Yonsei Med J 2004;45:1-6. |
|27.||Mandelbrot L, Le Chenadec J, Berrebi A, Bongain A, Bénifla JL, Delfraissy JF, et al. Perinatal HIV-1 transmission: Interaction between zidovudine prophylaxis and mode of delivery in the French Perinatal Cohort. JAMA 1998;280:55-60. |
|28.||Hebert PR, Reed G, Entman SS, Mitchel EF Jr, Berg C, Griffin MR. Serious maternal morbidity after childbirth: Prolonged hospital stays and readmissions. Obstet Gynecol 1999;94:942-7. |
|29.||Avidan MS, Jones N, Pozniak AL. The implications of HIV for the anaesthetist and the intensivist. Anaesthesia 2000;55:344-54. |
|30.||Morris A, Creasman J, Turner J, Luce JM, Wachter RM, Huang L. Intensive care of human immunodeficiency virus-infected patients during the era of highly active antiretroviral therapy. Am J Respir Crit Care Med 2002;166:262-7. |
|31.||British Thoracic Society Standards of Care Committee. BTS Guidelines for the Management of Community Acquired Pneumonia in Adults. Thora×2001;56 Suppl 4:IV1-64. |
|32.||Casalino E, Wolff M, Ravaud P, Choquet C, Bruneel F, Regnier B. Impact of HAART advent on admission patterns and survival in HIV-infected patients admitted to an intensive care unit. AIDS 2004;18:1429-33. |
|33.||Crothers K, Huang L. Critical care of patients with HIV. HIV in site knowledge base chapter; 2003. Available from: http://www.hivinsite.ucsf.udu/InSite. [Last accessed on 2011 June 14]. |
|34.||Mrus JM, Braun L, Yi MS, Linde-Zwirble WT, Johnston JA. Impact of HIV/AIDS on care and outcomes of severe sepsis. Crit Care 2005;9:R623-30. |
|35.||Vizcaychipi M, Keays R, Soni R. Anaesthesia and intensive care for HIV patients. Anaes Intensive Care Med 2006;8:44-7. |
|36.||Masur H. Management of patients with HIV in the intensive care unit. Proc Am Thorac Soc 2006;3:96-102. |
|37.||Centers for Disease Control (CDC). Update: Universal precautions for prevention of transmission of human immunodeficiency virus, hepatitis B virus, and other bloodborne pathogens in health-care settings. MMWR Morb Mortal Wkly Rep 1988;37:377-82, 387-8. |
|38.||Panlilio AL, Cardo DM, Grohskopf LA, Heneine W, Ross CS, U.S. Public Health Service. Updated U.S. Public Health Service guidelines for the management of occupational exposures to HIV and recommendations for postexposure prophylaxis. MMWR Recomm Rep 2005;54:1-17. |
|39.||Parthasarathy S, Ravishankar M. HIV and anaesthesia. Indian J Anaesth 2007;51:91-9. |
|40.||Kurosawa S, Kato M. Anesthetics, immune cells, and immune responses. J Anesth 2008;22:263-77. |
|41.||Mudido PM, Georges D, Dorazio D, Yen-Lieberman B, Bae S, O′Brien WA, et al. Human immunodeficiency virus type 1 activation after blood transfusion. Transfusion 1996;36:860-5. |
[Table 1], [Table 2], [Table 3], [Table 4]