Community acquired pneumonia implies pneumonia that is contracted outside of a medical facility or a long-term facility [30]. The 2005 American Thoracic Society (ATS) / Infectious disease society of America (IDSA) guidelines for the management of ventilator-associated pneumonia and hospital-acquired pneumonia included healthcare-associated pneumonia (HCAP) as a distinct clinical entity that required special antibiotic treatment. Patients with any of the following potential risk factors for antibiotic-resistant pathogens were classified as having HCAP: living in a nursing home or other long-term care facility; being hospitalized for more than two days within the previous ninety days; receiving chronic dialysis, home infusion therapy, home wound care; or having a family member with a known antibiotic-resistant pathogen. In order to choose extended antibiotic coverage for patients with CAP, the prior categorization of HCAP should be avoided. This primarily motivates a desire to address the misuse of anti-methicillin resistant Staphylococcus aureus (MRSA) and antipseudomonal therapy that has happened since the introduction of the HCAP categorization. The elderly age group is more prone to be affected by CAP and has several co-morbidities, both of which might raise the likelihood of unfavorable outcomes and subsequently result in the excessive use of healthcare resources and cost [31]. According to the ATS, for the treatment of CAP in previously healthy patients without risk factors for drug-resistant Streptococcus pneumoniae (DRSP) infection, the use of a macrolide antibiotic such as azithromycin, clarithromycin, or erythromycin is strongly recommended [32]. Presence of co-morbidities would require the usage of a respiratory fluoroquinolone (moxifloxacin, gemifloxacin or levofloxacin or a combination of β-lactam antibiotics plus a macrolide) [33]. β-lactam antibiotics can either be a high dose amoxicillin or amoxicillin-clavulanate or alternatives like ceftriaxone, cefpodoxime, and cefuroxime. For ICU treatment, a β- lactam antibiotic (cefotaxime, ceftriaxone, or ampicillin-sulbactam, Pipericillin + Tazobactam and Cefoperazone + Sulbactam) plus either azithromycin or fluoroquinolone is strongly recommended [32]. Data from the physician survey reporting commonly prescribed medications support recommendations made by ATS guidelines after ruling out Pulmonary Tuberculosis. The choice of the medications is influenced by the severity of the condition and the presence or absence of risk factors for Pseudomonas and MRSA along with the host’s factors like age and comorbidities which support recommendations made by ATS guidelines.
The study also assessed the clinical progression of CAP in adults by chronicling the burden of CAP in patients’ up to 90 days after diagnosis from patients’ perspective. The study also weighed the economic impact of CAP primarily based on the symptom severity and the correlation between treatment costs and risk variables. The primary results indicate that CAP patients had an array of systemic and respiratory symptoms that impact the development of other concurrent illnesses. Participants also reported worsening of existing co-morbid ailments like high blood pressure, diabetes, COPD due to CAP in both hospitalized and non-hospitalized patients. Hospitalized patients and non-hospitalized patients both experienced cough, tiredness, body ache, pain and weakness. Systemic symptoms like weak appetite, trouble sleeping, wheezing took a longer time to resolve in the non-hospitalized patients as opposed to hospitalized patients. Respiratory symptoms like pain from coughing, thick mucus or phlegm with cough shortness of breath were resolved in a shorter duration of time in hospitalized patients. This might have been on account of the fact that hospitalized individuals were more likely to receive nebulization; and also that there was a lower threshold for the prescription of systemic steroids in such of those patients with a background of asthma and COPD in the hospitalized patients. Additionally, the findings demonstrate that symptoms and their consequences might persist for days to weeks following the onset of sickness, inflicting a strain on patients as well as their caregivers and partners.
Our results can have an impact on a clinical practice since they offer insights from the patients’ point of view on the complexity of CAP symptoms, functional restrictions, and the amount of time required to fully recover. A greater understanding of the natural progression of CAP can help patients and medical professionals manage episodes that extend beyond the acute stage of the condition. Our data reveal a wider spectrum of symptoms that encompasses trouble in sleeping, tiredness, weak appetite, confusion, or trouble in sleeping than the usual pneumonia symptoms of cough, chest discomfort, and shortness of breath, suggesting that clinicians must solicit a wider range of symptoms. Further research might determine whether certain therapies are more efficacious than others at alleviating the various CAP symptoms. The quest for patient-centered outcomes that accurately reflect the patient’s experience is now an indispensable stimulus of health care reform.
Furthermore, even though the CAP-BIQ collects information to provide a thorough picture of the course of illness and impact of the disease from the perspective of the patient, this extensive questionnaire might not prove to be a congruous outcome metric in clinical trials for scrutinizing the therapeutic efficacy of varied treatments for pneumonia. However, the outcomes from this patient-reported outcome questionnaire may assist in the building of a more concise instrument for use in clinical studies assessing the impact of CAP at diagnosis and recovery. The studies that deploy the CAP-BIQ serve as the foundation for studies to generate a prospective patient-reported outcome for clinical trials in patients who have confirmed CAP radiographically. Patients’ awareness of the disease progression allows a more realistic anticipation of their recovery path. It might eliminate superfluous medical care and erroneous antibiotic prescriptions for unexpected recurrent episodes that actually mirror the illness’ typical course. However, this study has a few limitations. Like previous studies, retrospective collection of symptoms was used in this which is prone to recall bias. A window of 90 days between diagnosis and patient survey completion was necessary to recruit an adequate cohort of adults. Furthermore, though the study was conducted at seven medical centers across India, findings from the study were based on data from 188 patients thereby limiting the generalizability of the results. Moreover, the study primarily focused on hospitalized patients, leading to an underrepresentation of non-hospitalized cases, rendering the non-hospitalized cohort too small for drawing significant inferences. Additionally, the study predominantly involved patients from private hospitals, potentially skewing the findings in terms of cost implications and healthcare access, thus presenting a lopsided perspective on the economic burden. Future studies need to be conducted with a larger set of patients. Also, future studies need to be conducted enrolling more government medical centers to get an accurate representation of treatment patterns, symptom burden, healthcare resource utilization and costs. Despite these drawbacks, the study renders an array of pertinent insights regarding the burden of CAP as experienced by patients, a perspective which is often overlooked.